gms | German Medical Science

GMS Current Topics in Otorhinolaryngology - Head and Neck Surgery

German Society of Oto-Rhino-Laryngology, Head and Neck Surgery (DGHNOKHC)

ISSN 1865-1011

Pathophysiology of chronic rhinosinusitis, pharmaceutical therapy options

Review Article

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  • corresponding author Claus Bachert - Department of Otolaryngology and Upper Airways Research Laboratory, University of Ghent, Belgium; Division of ENT Diseases, CLINTEC, Karolinska Institute, University of Stockholm, Sweden
  • Gabriële Holtappels - Department of Otolaryngology and Upper Airways Research Laboratory, University of Ghent, Belgium

GMS Curr Top Otorhinolaryngol Head Neck Surg 2015;14:Doc09

doi: 10.3205/cto000124, urn:nbn:de:0183-cto0001242

Published: December 22, 2015

© 2015 Bachert et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution-Share Alike 4.0 License. See license information at http://creativecommons.org/licenses/by-sa/4.0/.


Abstract

Research in immunology has brought great progress in knowledge of inflammatory processes in the last 2 decades, which also has an impact on the upper airways. Our understanding of the pathophysiology of chronic rhinosinusitis developed from a rather mechanistic point of view with a focus on narrow clefts and mucociliary clearance to the appreciation of a complex network of immunological pathways forming the basis of disease. We today differentiate various forms of inflammation, we start to understand complex immune-regulatory networks and the reasons for their failure, and have already developed innovative approaches for therapy for the most severely ill subjects. Due to this new knowledge in inflammation and remodeling processes within mucosal tissue, specifically on the key driving factors, new diagnostic tools and therapeutic approaches for chronic rhinosinusitis have developed; the differentiation of endotypes based on pathophysiological principles will be crucial for the use of innovative therapies, mostly humanized monoclonal antibodies. Several hundred of those antibodies are currently developed for various indications and will impact our specialty as well as pneumology to a great extent.

Keywords: chronic rhinosinusitis, pathophysiology, cluster analysis, phenotypes, endotypes, Staphylococcus aureus, biologics


1 Introduction: From pathophysiology to endotypes of chronic rhinosinusitis and their treatment

Chronic rhinosinusitis (CRS) describes a heterogeneous group of diseases of the nose and the paranasal sinuses that is characterized by two phenomena: inflammation and tissue remodeling. According to the European position paper on rhinosinusitis and nasal polyps [1], CRS is defined by the presence of at least two of the following symptoms: nasal obstruction, nasal secretion and/or post-nasal drip (PND), headaches and/or facial pains, a reduction of smelling for more than 12 weeks during the last year while at least one of the first two mentioned symptoms should be observed. The burden of the symptoms, the associated reduction of the quality of life and the influence of the disease on work productivity are often underestimated. With reference to the endoscopic findings, the difference is made between the clinical phenotypes of CRS without and CRS with nasal polyps (CRSsNP, CRSwNP) [1]. Recent findings on remodeling confirm this differentiation and reveal that there are significant differences between the phenotypes. Histologically, CRSsNP is characterized by fibrosis of the mucosa and the basal membrane while nasal polyposis is characterized by important edema with deposition of albumin and the development of pseudocysts. The differentiation of the inflammation types based on T helper cells allows a more differentiated classification according to pathomechanical principles into so-called endotypes within the clinical phenotypes which can finally be used to define innovative therapeutic objectives and to implement them in daily clinical routine.

CRS is one of the most frequently occurring diseases in humans. Recently, the Global Allergy and Asthma Network of Excellence GALEN [2] published a first multicenter prevalence study on chronic rhinosinusitis that is based on 56,000 questionnaires that were returned by 19 centers in 12 European countries; a random sample was also submitted to clinical examination by a specialist in order to confirm the diagnosis [3]. The investigation came to the conclusion that the prevalence of CRS in Europe amounts to 10.9%, between 6.9 and 27.1% in different European cities [4]. Higher prevalences were discovered in younger people, women, and southern countries; smoking significantly increased the risk for CRS, depending on the dose. In the USA the prevalence is even higher [5]. CRS, however, also affects and increased part of the older population up to the age of 60, afterwards the incidence decreases. Among all CRS patients in the USA, about 20–33% suffer from CRSwNP, 60–65% suffer from CRSsNP, and 8–12% from allergic fungal sinusitis (AFS).

One important finding of the GALEN study on chronic rhinosinusitis was that CRS is associated with an increased risk for a special type of asthma, i.e. a so-called late-onset asthma or asthma occurring after the age of 18 [6]. This association was independent from an existing allergy, in contrast to asthma in early childhood which is clearly associated with allergic rhinitis. The exact pathophysiology of this observation is not known up to now. Mechanisms could consist of the nasobronchial reflex, aspiration of nasal secretion, inhalation of cold air with obstructed nose, or the progress of the inflammation along the airway mucosa. The research program established in the USA entitled “Severe Asthma Research Program (SARP)” recently identified five different asthma phenotypes in a cluster analysis; in one of the clusters with non-atopic late-onset asthma, more than half of the patients reported about interventions of the paranasal sinuses [7]. Another investigation of 2,500 asthmatics revealed that about 51% had rhinosinusitis; CRS was associated with a deterioration of coughing symptoms and with a higher number of exacerbations [8]. Those results confirm the relationship between CRS and asthma; however, it remains unclear for which type of CRS they are true and which pathomechanisms are responsible.

Further it is well-known that part of the patients with CRS will have recurrences even after well performed surgery and will have to undergo another surgical intervention – or innovative therapeutic approaches (see the following chapters) [1]. Own observations show that nearly 80% of CRSwNP patients develop at least one recurrence over a time of 12 years after complete surgery of all paranasal sinuses and removal of all polyps. About 50% of those patients have to undergo at least one further surgery (data not published). It would be desirable to understand the pathomechanisms of this disposition to develop recurrences and to recognize patients with a high disposition in the group of CRSwNP patients already at the time of first surgery [9] in order to be able to adapt treatment strategies.

It is not possible to fulfill this task only with endoscopes and CT scans; a basic knowledge of the pathomechanisms of inflammation and of remodeling is required as well as differentiation of CRS into relevant endotypes based on this knowledge. In the future biomarkers will be applied for their identification. The understanding of the pathomechanisms will also define new therapeutic objectives that will open new possibilities for the management of especially severe types of airway diseases. Those endotypes will allow to give statements on the prognosis of the disease and their comorbidities and to apply specific innovative biologics, generally humanized monoclonal antibodies for cytokines or their receptors, in those patients who have the highest therapeutic potential.

The present paper will first discuss the significant aspects and regulators of inflammation and remodeling that are then attributed to the different endotypes on which finally innovative therapeutic approaches are based. In this context, very special pathomechanisms and relationships are explained that play a role in the development of endotypes and that help understanding the diseases and their secondary consequences. Also the innovative therapeutic approaches will be understandable and clear. However, those explanations make no claim to be complete.


2 Selected pathomechanical principles of the upper airways

The mucosa of the upper airways represents a barrier of the body between the environment with pollutants, viruses, and bacteria and the body’s defense system that can be classified into an unspecific “innate” and a specific “adaptive” defense. Overlapping of these systems is profitable. Starting with genetics via the innate and adaptive defenses up to the mechanisms that act against inflammation in healthy people, deficits were found in CRS patients that in total cause or at least allow an affection of the mucosa. In the environment, those defects have to face invading substances, viruses, and bacteria that complete and potentiate each other and that, as for example in the case of Staphylococcus aureus and Pseudomonas aeruginosa, may establish in the mucosa. This mechanism leads to a severe inflammatory reaction that in case of Staph. aureus is further intensified by the immune proteome of the germ.

2.1 Genetic and epigenetic findings in chronic rhinosinusitis

Single nucleotide polymorphism (SNP) is a variation of the DNA sequence where the genome of individuals of a biologic species is different in the position of one single nucleotide – A, T, C, or G. Such genetic variations are for example responsible for predispositions of diseases and the body’s reaction on environmental stimuli. Up to now, studies on CRS identified 53 single nucleotide polymorphisms (SNP) that are associated with the phenotypes of CRSwNP or CRSsNP. However, only a pooled genome-wide association study (pGWAS) was performed [10]. Most association studies (see Table 1[Tab. 1]) examined only specific genes of which the products contribute to the innate immune defense or inflammatory reactions because findings in those genes are probable in the context of inflammatory diseases. Unfortunately, many of those studies including the Canadian pGWAS (173 patients and 130 controls with CRS) were based on patient populations of relatively small size so that the knowledge on the genetics of CRS is rather limited [10], [11].

Recently we investigated on the reproducibility of all SNP associations with CRSsNP and CRSwNP described up to now in a group of Caucasians of European origin [12]. According to the current guidelines, CRS had been diagnosed based on nasal endoscopy and computed tomography. The study population consisted of 275 patients with CRSwNP and 338 patients with CRSsNP as well as a series of controls from a publicly available database. This study provided only 7 SNPs that could be reproduced and that are thus most probably also relevant for our patients; however, the existence of further relevant associations cannot be excluded.

Regarding the SNP Rs2873551 in the gene of prolyl tRNA synthetase 2 (PARS2), there was a strong and significant relationship with CRS; this SNP had already been identified in the Canadian pGWAS. PARS2 activates amino acids for protein synthesis by producing aminoacyladenylates. Inhibition of the function of PARS2 causes suppression of the cellular growth and could have an impact on the cellular proliferation in combination with inflammatory processes and the innate immune defense. The SNP rs1800469 in the gene of TGF-β1 has been associated with chronic obstructive pulmonary disease and rhinosinusitis in asthma patients [13]; this cytokine will be discussed later in the context of remodeling of CRS. Also SNP rs1483757 in the nitric oxide synthase 1 gene and the SNP rs4657164 in the nitric oxide synthase 1 adapter protein gene are associated with CRS and are also found in genes that play a role in asthma and allergic rhinitis [14]. Nitric oxide also plays an important role in the pathophysiology of asthma [15] and in the defense against specific bacteria including Pseudomonas aeruginosa [16].

Comparing CRSwNP and CRSsNP patients, further associations could be found. The SNP rs4504543 in the gene of acyloxyacylhodrolase (AOAH) could lead to a disturbed degradation of lipopolysaccharides [17]. In the pGWAS, this SNP had already been related to the CRS phenotype [10] which was confirmed by a Chinese patient population [17]. Furthermore, an association with asthma was identified [18].

So it is obvious that the genetic variations that were found in our investigation had already been associated with CRS and partly also with asthma or allergic rhinitis and thus could play a role in diseases of the airways. The detected associations, however, are independent from the aspect if patients suffer from asthma or allergic rhinitis. The SNPs in the gene of PARS2, in the gene of TGF-β1, and in the NOS1 gene are suitable candidates for further analyses because also from a biological point of view they are plausible.

Also in the context of epigenetic processes that significantly influence the development and manifestation of the pattern of the inflammation, tissue specific chronic inflammatory processes are subject to modifications. Epigenetic mechanisms are classified into DNA methylation, histone acetylation, and the formation of non-coding RNA, so-called miRNA, that influences the expression of other genes. This is another level of regulation between genes and proteins that can decisively be modified by inflammatory processes and also by the environment.

Among others, epigenetic processes lead to functional modifications in the genome without change or modification of the basic DNA nucleotide sequence. Examples of such modifications are DNA methylation and histone modifications that both lead to a reduction of the expression of a gene; however, this may result in an amplification or attenuation of the inflammation, depending on the genes that are expressed in a reduced way. A first investigation on methylation modifications in CRSwNP found DNA hypermethylation in 332 loci of 296 genes. The relevant gene products contributed to lymphocyte and cellular proliferation, to the activation of leukocytes, to the biosynthesis and secretion of cytokines, to immune reactions, to inflammatory processes, and to the immunoglobulin synthesis [19]. In comparison, hypomethylation was identified in 158 loci of 141 genes with involvement in ectodermal development, in hemostasis, in wound healing, in the binding of calcium ions, and in oxidoreductase activity. It is of high significance that within the arachidonic acid metabolism loci were hypomethylated in genes responsible for prostaglandin-D-synthase (PDGS), for 5-lipoxidenase activating protein (ALOX5AP), and for leukotriene-B4 receptor (LTB4R), while hypermethylation was found in the gene for prostaglandin-E-synthase (PGES) [19]. DNA methylation processes can be initiated by the release of toxic messenger substances because of the activation of eosinophils [20] that may lead to gene silencing by expressing hypohalogenous acids; they are the consequence of eosinophilic diseases, histone hyperacetylations can lead to an inhibition of the TGF-β1 induced Smad 2/3, to the restoring of Smad7 signal suppressed by TGF-β1, and to a blockage of the proliferation of TGF-β1 induced nasal polyp fibroblasts [21], [22].

The genetic transcription is also regulated by non-coding RNA, e.g. by micro RNA and by long, non-coding miRNA. An increased expression of miR-125b in the epithelium of eosinophilic CRSwNP patients in comparison to controls and non-eosinophilic CRS patients, for example, aims at 4E-BP1, a translation repressor, suppressing type-1 interferon genes [23]. Those genes are needed for the defense against viral infections. This defense can be disturbed in those patients (actually a suppression of IFN production against herpes simplex viruses (HSV) and rhinoviruses in patients with eosinophilic nasal polyposis is found, in contrast to control groups, see 2.5.1).

In an own investigation we assessed the regulation of an inflammation in two well-defined endotypes, interleukin(IL)-5-positive and IL-5-negative CRSwNP, by miRNAs in a genome-wide approach by means of miRCURY LNA microarray platform in mucosal tissue. A total of 86 miRNAs were differentially expressed and could be classified into 5 different profiles; the investigation indicates regulatory mechanisms in the mucous production, the collagen synthesis, the cytochromes P450, and the glycosphingo-lipid-biosynthesis that is regulated via miRNAs (Zhou Peng, in press). Hence, there are new possibilities to examine further pathomechanisms, and probably therapeutic approaches in the future, because miRNAs can also be blocked.

2.2 Congenital immune defense: mechanisms and deficits

The upper airways are covered by a mucosal layer consisting of ciliated, pseudo-stratified columnar epithelial cells (EC) and mucus producing goblet cells. The drainage of the mucus is achieved by active mucociliary activity, not by gravitation. The mucosa is covered by mucus where micro-organisms, dust, and stimulating particles get caught. Nasal secretion consists of epithelial cells, goblet cells, epithelial cell proteins, lacrimal fluid, and vascular transudation. The primary protein parts of this secretion are mucin glycoproteins with their peptide structure and the oligosaccharide side chains. Those glycoproteins decisively influence the consistency of the mucus and furthermore they influence the interaction between host and microorganisms [24]. Mucins bind surface adhesins on microorganisms and thus inhibit their capacity to colonize the epithelium. Mucociliary activity transports the mucus from the paranasal sinuses into the nasal cavity and the pharynx where it is swallowed. The relevance of this process for the health of the airways becomes obvious in the high prevalence of sinusitis in patients with genetic defects influencing the mucociliary flow, as for example in cases of cystic fibrosis (chloride transport) or Kartagener syndrome (dyskinesia of the cilia). The nose has a large mucosal surface with a mucus layer that filters air particles and tempers and moistens the air flowing over it. In the nasal submucosa, vascular plexus are found that swell after exposition to certain triggers such as stimuli, temperature changes etc.; further more mucus is produced.

Mucin 5AC and mucin 5B are the most important secreted mucins and determine the consistency of the mucus significantly. Both are especially up-regulated in eosinophilic CRSwNP. Recently we could show that the regulation of both mucins occurs via the Th2 cytokines IL-4 and IL-13 while IL-5 has no influence [25].

2.2.1 Antimicrobial peptides

Epithelial cells release a wide range of antimicrobial molecules, as for example enzymes (lysozyme, chitinases, and peroxidases), opsonins (complement and pentraxin-3), permeabilizing proteins (defensins, cathelicidins), C1 complexes (surfactant protein A, surfactant protein D, and mannose-binding lectin), and ligands (lactoferrin and mucins) [26], [27]. Beside their antimicrobial effect they have different other effects on cellular differentiation and wound healing [28]. The protein PLUNC (palate, lung, and nasal clone protein) is secreted by glandular epithelium and not by surface epithelium. Probably it is of particular importance for airway diseases because it has biofilm inhibiting properties.

A weak host defense could be the result of a primary defect of the innate immunity in the paranasal sinuses, but it is also possible that it is a consequence of chronic eosinophilic airway inflammation. There are hints that Th2 cytokines might down-regulate the production of mediators of the innate immunity, such as for example human beta defensing 2 and surfactant protein A [29]. Other cytokines, in particular T cell cytokine IL-22, induce mediators of the innate immune defense in epithelial cells by activating STAT3 (transcription factor signal transducer and activator of transcription 3) which is a mediator of mucosal host defense and epithelial repair mechanisms [30], [31]. Th2 polarization may lead to a reduced expression of IL22 receptor and STAT3 signal pathway [32], [33].

Also taste receptors (taste receptor family 2 (T2R)), also called “bitter taste receptors”, that were first described in the tongue, are expressed in the airways and assess toxic chemicals but also signal of bacteria they release for communication among each other. In this way, the receptor T2R38 is activated by secreted products of Pseudomonas aeruginosa which leads to the induction of nitric oxide and finally to bacterial death [34]. Genetic defects of the receptor increase the risk of infection with gram-negative germs.

2.2.2 Epithelial barriers

Respiratory epithelial cells are connected via adhesion complexes, consisting of apical tight junctions, intermediate junctions, desmosomes, and hemi-desmosomes. A reduced expression of the tight junction proteins of claudin and occludin [35] or desmosomal proteins [36] can play a key role in the etiology of diseases of the upper airways. Reduced concentrations of protease inhibitors, such as the serine protease inhibitor Kazal type 5 (LEKT1), in the epithelium may lead to an increased sensitivity for the activity of endogenous and exogenous proteases [37]; fungi, bacteria, and many allergens dispose of a significant intrinsic protease activity. A simultaneous weakness of endogenous protease inhibitors such as LEKT1 could have the effect that the mechanical barrier cannot counter a protease attack so that foreign proteins can pass the mucosal barrier more easily.

In nasal polyps, occludin, the Zonula occludens 1 protein, and E-cadherin are expressed in a reduced way so that the epithelial barrier can be passed more easily by viral and bacterial infections [38], [39] (Figure 1 [Fig. 1]).

2.2.3 Receptors of congenital immune defense: Toll-like, NOD-like, and RIG-like receptors

Epithelial cells of the nose and the paranasal sinuses do not only represent a physical barrier, but have active functions in the context of innate and acquired immune defense [40]. They express membrane-bound and cytoplasmatic pattern recognition receptors (PRR) that recognize pathogen-associated molecular patterns (PAMPs) [41]. The activation of those receptors leads to the release of chemokines and cytokines and components of the innate immune system activating further immune cells (for example neutrophils). Different microbial factors or PAMPs, such as for example bacterial lipopolysaccharides (LPS), flagellin, lipoteichoic acid, peptidoglycan, double stranded RNA, and unmethylized CpG motives, can be recognized by many PRRs [42]. The activation of PRRs in the nasal epithelium may lead either to the induction of tolerance or to the expression of inflammatory mediators attracting neutrophil lymphocytes.

Several groups of such receptors were described recognizing PAMPs, among them toll-like receptors (TLR), nucleotide-binding oligomerisation domain (NOD) like receptors, retinoic acid induced gene (RIG)-1-like receptors, and the melanoma differentiation associated gene (MDA)-5. The complex of TLR currently encompasses 10 integral membrane glycoproteins that recognize extracellular and intracellular PAMPs [43]. All TLR signaling pathways lead to activation of the transcription factor NF-κB (nuclear factor kappa B) which controls the expression of numerous genes for inflammatory cytokines. Obviously, all TLR are expressed in the healthy nasal mucosa as well as in cases of CRS [44]; however, the expression of TLR2, TLR4, and TLR9 receptors and their effector molecule NF-κB in the mucosa of CRS patients is higher compared to healthy people [41], [44], [45], [46]. Disturbed expression of those receptors may contribute to the development of CRS [47].

Intracellular PAMPs, such as for example muramyl dipeptide (MDP) and peptidoglycan are recognized by NOD-like receptors. NOD-like receptors are expressed in the epithelial cells of the nose and the paranasal sinuses [48]. Epithelial cells further express protease-activated receptors (PAR) [49] that are activated by different endogenous and exogenous proteases, including those that are associated with bacteria, fungi, and allergens [50]. The activation of PAR also induces the NFκβ signaling pathway [51]. Proteases of Staphylococcus aureus activate PAR-2 and lead to a release of interleukin (IL)-8 [49], [52]. In cases of chronic airway diseases, epithelial cells express more PAR2 than under healthy conditions [49].

2.2.4 Indicators of cellular death: damage-associated molecular patterns (DAMPs)

Beside pathogen-associated molecular patterns (PAMPs), cells also recognize cellular damages because of their damage-associated molecular pattern (DAMPs). The combination of foreign material plus cellular damages triggers a reaction of the innate immune system and activated the adaptive immune defense or contributes substantially to its manifestation [53].

In addition to actively secreted inflammatory messengers, recently also those messengers are in the focus of scientific attention that are part of the endogenous intracellular or extracellular matrix of the host and can be released passively into the extracellular space. When released, the original functions of those components change so that they modulate inflammatory reactions under pathologic circumstances in their new environment. In analogy to the PAMPS, those molecules were named DAMPs [54], [55], [56].

Intracellular molecules with extracellular DAMP function are released either passively by damaged cells during an inflammatory or infectious event or actively by certain cell types via so-called alternative secretory pathways because per definition the leader sequence for secretion is missing [56]. DAMPs from the extracellular matrix of the host can be released in cases of damage or by regulated shedding mechanisms [57]. Currently, more than 40 molecules have been classified as DAMP. They exert their effect through activation of at least one toll-like receptor (TLR) or other members of the PRR family, for example via “scavenger receptors” (e.g. CD36) or specialized receptors such as RAGE receptor (receptor for advanced glycation end products) [57]. Several DAMPs also bind to ECM structures like heparan sulphate proteoglycans [56], [57] (Table 2 [Tab. 2]).

Concerning the upper airways, up to now from all known DAMPs and their respective receptors, only the multi-ligand receptor RAGE has been examined intensively [58]. RAGE is a cellular surface protein that is part of the immunoglobulin superfamily and that is made responsible for different inflammatory reactions. RAGE is expressed in full length as membrane-bound receptor (mRAGE), but it also appears as two soluble forms without transmembranous or cytoplasmatic domain; together they are called “sRAGE”. sRage originating from alternative mRNA splicing is classified as “endogenous secretory RAGE” or esRage while RAGE occurring from proteolytic splitting of mRAGE is called cRAGE; this process is initiated by metalloproteinases (MMPs) and ADAMs (A Disintegrin And Metalloproteinases) [59], [60], [61].

mRAGE binds to several ligands, for example to AGE products (advanced glycation end products), HMGB1 (high mobility group box 1), members of the S100/Calgranulin family, the Integrin Mac-1, and to ECM structures such as heaparan sulphate proteoglycans (HSPGs) [62]. sRAGE, on the other hand, seems of act often as kind of a bait receptor with inflammation-inhibiting properties by “intercepting” RAGE ligands of mRAGE surface receptors that transduces inflammatory reactions via the transcription factor NF-κB [63], but it can also promote the inflammation [64]. For mRAGE, too, certain inflammation-inhibiting characteristics have been described [65].

Under normal physiological conditions, RAGE is expressed to a high degree in the lungs – in contrast to many other tissues [65], [66]. In humans, RAGE is also highly expressed in the upper airways under normal physiological conditions and in cases of chronic inflammations it is subject to differential regulation. In CRSsNP, the sRAGE protein quantities are increased whereas the quantity of mRAGE is reduced compared to the control groups. In CRSwNP, the sRAGE and mRAGE protein quantities are reduced in the tissue [58] which is due to an imbalance of metalloproteinases and their natural inhibitors (TIMPs) [67].

Because of the relative lack of collagen in CRSwNP and the excessive collage production with thickening of the collagen fibers in the extracellular matrix (ECM) in CRSsNP [21], [67], the fibrotic tissue has higher quantities of sRAGE than pseudocystic tissue of CRSwNP patients because sRAGE bind to those structures in the long term [66], [68]. In CRSwNP patients, the increased colonization incidence of Staph. aureus may contribute to further reduction of sRAGE [69] because Staph. aureus induces the release of sRAGE from the ECM [58]. The higher amount of ECM-associated sRAGE in CRSsNP induces an inflammation that is polarized in direction of Th1 [58]. RAGE participates in the differentiation of T cells to a Th1-phenotype; if RAGE is missing, the production of Th1 cytokines is reduced while more Th2 cytokines are produced [70]. Additionally, in CRSwNP a higher amount of protein is found of eosinophil-cationic protein ECP that degrades non-ECM-associated sRAGE so that a reorientation of T helper cells in direction of Th1 is inhibited [58].

Calcium-binding proteins S100A7 (psoriasin), S100A8 (MRP8 or calgranulin A), S100A9 (MRP14 or calgranulin B) and their heterodimer types of S100A8/A9 (calprotectin) have been examined in CRS patients because of their antimicrobial effect [28], [37]. S100 proteins have the typical properties of DAMPs when they are released into the extracellular milieu where they activate TLR4 [71], [72] and possibly also RAGE [73]. In comparison to healthy people, the expression of S100A7, S100A8, and S100A9 mRNA is reduced in patients with CRSsNP and CRSwNP [74]. S100A7 proteins are reduced in the epithelium and in glandular structures in CRSwNP and also the nasal lavage fluid of those patients shows low quantities of S100A7 [37]. In comparison, the amount of heterodimer S100A8/A9 proteins is extremely increased in the polypous tissue because of the higher infiltration of neutrophils, which is a main source of S100A8/A9 proteins [37]. These results indicate that secreted S100A7 and S100A8/A9 proteins from epithelial and/or glandular tissue play a role as antimicrobial substance in the paranasal sinuses and allow the hypothesis that reduced quantities are a possible key to CRS pathogenesis.

Fibronectin is a macromolecular glycoprotein of the extracellular matrix that is very important in the context of wound healing, cell adhesion, matrix formation, protein secretion, cell differentiation, cell cycle progression, and mitogenous signal transduction [75], [76]. It is also associated with immune processes that occur via activation of TLR4; it then has the effect of DAMP [77]. Fibronectin is also considered as target molecule of a high number of bacterial proteins, the bacterial fibronectin binding proteins (FnBPs) [78]; it mediates the adherence of Staph. aureus to the extracellular matrix and to the surface of host cells, for example to endothelial cells, epithelial cells, and fibroblasts, through which Staph. aureus can enter into the cytoplasm of those cells [78], [79]. Inside the cell, Staph. aureus is protected against antibiotics and the immune reactions of the host [79] and thus it can survive which in view of the increased fibronectin expression [39] and the high colonization rate with Staph. aureus explains the intramucosal presence of bacteria especially in CRSwNP patients [69].

2.2.5 Lymphoid cells of innate immune defense (ILCs, innate lymphoid cells)

Epithelial cells in the airways produce numerous inflammatory cytokines as normal reaction of the stimulation of PAMP and DAMP receptors [51], among those IL-1, tumor necrosis factor α (TNF-α), type 1 interferons (IFN-α/β), granulocyte macrophage colony stimulating factor (GM-CSF), eotaxins, RANTES (regulated upon activation normal T-cell expressed and secreted), IFN-γ-inducible protein 10 (IP-10), IL-6, IL-8, the growth-regulated oncogene α (GRO-α), monodansylcadaverine (MDC), stem cell factor (SCF), TARC (thymus and activation regulated chemokine), monocyte chemotaxis protein 4 (MCP-4), B cell activating factor (BAFF), osteopontin, IL-32, and Th2 immune reaction associated cytokines such as IL-25, IL-33, and TSLP (thymic stromal lymphopoietin) [26], [49]. Those cytokines do not only cause tissue swelling, vascular dilation, and other characteristics of inflammations, but they often have also chemotactic properties, by which they attract different leukocytes, mast cells, neutrophils, dendritic cells, and lymphocytes to the locus of the inflammation. Also cytokines produced by epithelial cells play a major role in the polarization of dendritic cells and thus influence the type of T cell reaction on antigens [80]. Apparently, there are very special epithelial cell cytokines (IL-25, IL-33, and TSLP) that induce the polarization of dendritic cells and the subsequent T cell differentiation on mucosal antigens [80]. Those cytokines have the particular ability to influence the differentiation of T-cells in direction of Th2-profile as it is known from CRSwNP. Presumably, epithelial cells do not only contribute significantly to the mediation of reactions of the innate immune defense but also influence in this way the subsequent adaptive immune defense. Currently it cannot be excluded that the etiology and pathogenesis of CRS are based on primary variations of the reaction pattern of epithelial cells.

Lymphoid cells of the innate immune defense (innate lymphoid cells, ILCs) have important effector and regulation functions in the innate immune defense and remodeling of tissue, however, they do not perform receptor rearrangement (this property is termed “lineage negative”). ILCs are classified into three categories based on the characteristic patterns of the cytokines they produce and the transcription factors that are necessary for their development and function analogous to the T helper cells: Group 1 ILCs (ILC1) produce interferon γ and depend from the transcription factor Tbet, while group 2 ILCs (ILC2) can produce Th2 cytokines such as IL-5 and IL-13 and therefore need the transcription factor GATA3. Group 3 ILCs (ILC3) also comprise lymphatic tissue inducing cells. ILC3s can produce IL-17 and/or IL-22 and require RORγt as transcription factor. In this regard, ILCs are very similar to T helper cells, however, they are part of the innate immune defense and according to the current knowledge they form the link between epithelium and T cell compartment [81].

CRTH2 and ST2 (IL-33 receptor)-positive ILC2s have been detected in healthy human lungs; however, it is currently unclear which functions ILC2s have in humans in comparison to Th2 effector cells (that both produce IL-5 and IL-13) in the context of pulmonary hemostasis. Accordingly, CRTH2+ILC2s have been identified in CRSwNP tissue [82]. TSLP – an ILC2-activator produced by epithelial cells – is expressed to a high degree in epithelial cells of CRSwNP tissue in patient with asthma [83]. Only little is known about the function of other ILC subgroups in the airways.

In contrast, lipoxin A4, a lipid mediator with inflammation-resolving properties, via the inhibition of IL-13 production of ILC2s [84]. LXA4 also causes the number of eosinophils to decrease by favouring the NK cell mediated apoptosis of those cells. ILC2 localizes in the airways near the mast cells that release prostaglandin D2 (PGD2) which increases the IL-13 production of ILC2s via the PGD2 receptor CRTH2. Thus the activity of ILC2s is regulated by the balance between LXA4 on the one hand and PGD2 on the other hand, whereas both LXA4 and PGD2 are increased in CRSwNP. However, this balance is again disturbed in cases of aspirin sensitivity [85], [86].

2.2.6 Dendritic cells and macrophages

Dendritic cells (DCs) are the link between innate and adaptive immune defense on mucosa. In the airways, several functional subgroups of DCs have been described that differ with regard to their stage of maturity and the expressed combination of PRRs [87]. DCs recognize antigens and process and present them to antigen unversed or “naïve” T cells. Because of these functions, DCs play a key role in the fine adjustment of immune reactions and favor the production of Th1, Th2, or Th17 reactions or regulatory T cells (Tregs) [80]. In the nasal mucosa, 4 different DC subgroups could be identified: 2 myeloid DC populations (mDC) that express either BDCA1 (Blood Dendritic Cell Antigen 1) or BDCA2, a plasmacytoid population of dendritic cells (pDC) that is BDCA1 and CD123 positive (CD = cluster of differentiation), and BDCA1 and CD207 positive Langerhans cells [88]. In CRSwNP tissue where the inflammation pattern is polarized in direction of Th2, an increased number of mDCs and pDCs could be found [89]. This distribution pattern of DCs could contribute to the persisting airway inflammation in cases of CRSwNP.

Macrophages are cells of the innate immune defense that have various functions, as for example to remove particles, to primarily react on pathogens, to maintain tissue hemostasis, to coordinate the adaptive immune defense, to develop inflammation and tissue repair [90]. In accordance to the factor macrophages come in contact with, they polarize to a classically activated inflammatory M1 phenotype or to an alternatively activated M2 phenotype [91]. M1 macrophages express inflammatory cytokines to a high degree such as IL-1β, IL-12, IL-23, and TNF as well as effector molecules as nitric oxide. They contribute to the induction of Th1 reaction and inhibit the survival of pathogens by destroying them effectively inside the cells [92]. However, we could observe that macrophages in IL-5 expressing CRSwNP tissue were mainly M2 polarized and had a high expression of CD206 [93]. Remarkably, M2 macrophages were not able to perform phagocytosis nor to destroy germs like Staph. aureus, and this circumstance promotes the intracellular survival of those germs (see later). Furthermore, M2 macrophages from nasal polyps release high quantities of the chemokine ligand 18 (CCL18) which has a chemotactic effect on DCs, naïve T cells, and Th2 cells; all those cells contribute to the pathogenesis of CRSwNP [94] (Figure 2 [Fig. 2]).

2.3 Adaptive immune defense: T cells as central components

The adaptive immune defense consists on the one hand of T cells that are especially targeted for this challenge. They may be subdivided into several groups according to the released cytokines and their functions. On the other hand there is the B cell response that is targeted to the production of specific antibodies. The resulting T cell response should be subject to the regulation of T regulatory cells; if not, persisting inflammation occurs. Other bystander cells such as eosinophils and mast cells further modify and amplify the inflammation process, in particular in cases of Th2 reaction. Such cell components sum up the processes that finally lead to most severe diseases of the mucosa, mainly Th2 characterized.

2.3.1 T helper cell patterns

While CRSsNP appears as an only moderate, mainly neutrophil Th1 polarized inflammation, CRSwNP is characterized beside the neutrophil component by a moderate to high eosinopilic Th2 polarized inflammation, at least in Caucasians [95]. Presumably, the reduced TGF-β expression in the CRSwNP tissue contributes to a deficit of Tregs [13], [21], [96] like the strong expression of suppressor of cytokine signaling 3 (SOCS3) which is further enhanced by the reduced migration of regulatory T cells. SOCS3 and Foxp3, which is an important transcription factor of T regulatory cells, is co-expressed in Tregs; SOCS3 regulated Foxp3 expression probably via phosphorylation of STAT3 [96]. The relative deficit of Tregs could be the reason for the inability to suppress the eosinophilic inflammation in CRSwNP patients. In Caucasians, more than 80% of the polyps express a Th2 profile with clear expression of interleukin-5 protein and consecutive tissue eosinophilia whereas this profile is found in less than 20% of all central Chinese CRSwNP patients. Instead, there are Th17 cells that induce a mainly neutrophil inflammation reaction [97].

An extensive flow cytometry of the T cell subtypes was performed in the affected and healthy nasal mucosa in CRS patients [98]. Most of the T cells in the nasal mucosa were CD45RA negative and had an effector phenotype, whereas T cells in the blood mostly have markers of naïve T cell phenotypes. Both in the healthy and in the affected nasal mucosa, a heterogeneous population of T helper cells was present: Th1, Th17, Th22, and Tfh (follicular helper) cells were found. A certain plasticity of the T helper cells could be revealed because for example the Th17 cell population produced not only IL-17, but also IFN and IL-22. The reason for this heterogeneity among the effector T cells might be associated with their protector function, i.e. according to the type of the entering microorganisms, several optimal immune reactions should be possible. The results show that the T cell profile of CRSsNP specimens only differs little from the control specimens which confirms previous findings that CRSsNP is rather a remodeling process than a specific inflammatory reaction [21]. It was remarkable that Th2 cells could only be identified in CRSwNP specimens while asthma patients had the highest number of cells. This pattern correlates with protein data of homogenized tissue specimens after multiplex cytokine analyses [99]. Even if IFN gamma is the most important intracytoplasmatic cytokine in T cells, as protein only low concentrations can be detected in tissue homogenates; apparently IFN is not spontaneously released under basic conditions whereas high concentrations were found after stimulation in the cell free supernatant. IL-5, however, is only expressed by relatively few CD4 positive T cells, but regularly released spontaneously by a CRSwNP endotype; this spontaneous release can be significantly increased by intramucosal Staph. aureus germs (see later).

Beside CD4 positive T cells, there is a larger population of T cells in the nasal mucosa that belong to the CD8 cell line and that are the main source of IFN gamma. CD8 positive cytotoxic T cells (Tc cells) express high quantities of Fas ligand that may induce apoptosis in other cells. Another important function of IFN producing CD8 positive T cells (so-called Tc1 cells) is their ability to inhibit IgE response.

The presence of Th2 cells and the expression of IL-5 is associated with eosinophilia, an increased ECP (eosinophil cationic protein) and the total amount of IgE in the mucosa, independent of the atopic status of the patients [97]. The percentage of IL-5 positive nasal polys in Europe amounts to about 85% of all CRSwNP while the percentage in Central Asia, for example in China, is significantly lower with 15% [97]. IL-5 is important for the survival and activation of eosinophils and can be produced by lymphocytes, mast cells, and the eosinophils themselves [100]. The important role of IL-5 for the survival of eosinophils in nasal polyps was revealed in ex vivo trials with human nasal mucosa with neutralizing monoclonal anti-IL-5 antibodies that induced apoptosis in eosinophils and significantly reduced the synthesis of IL-5 and thus also the number of eosinophils. Based on this observation, we performed a pilot projects and studied the possibility to treat severe nasal polyposis with a humanized monoclonal antibody against IL-5 (Mepolizumab) [101]. Two single intravenous injections of 750 mg Mepolizumab led to a significantly improved nasal polyp score in comparison to a placebo group and to a reduction of the polypous mass revealed in computed tomography. This proof-of-concept study confirms the role of IL-5 in CRSwNP and proves the significance of biomarkers for the prognosis and thus the optimized patient selection (Figure 3 [Fig. 3]).

2.3.2 B cells and local immunoglobulin production

In CRSwNP, the total number of B and plasma cells such as the relation of plasma cells and B cells is partly much increased in comparison to control groups which might be a hint to an active B cell compartment in this disease, but not in CRSsNP [102]. In cases of eosinophilic CRSwNP, the local IgG and IgE concentrations, and important markers of a local immunoglobulin class switch are as well increased in comparison to allergic rhinitis and healthy people [103]; also this phenomenon is not observed in CRSsNP. During the immunoglobulin class switch, recombination events occur (class switch recombination, CSR) typically via IgG4 to IgE. In up to 30% of the B cells, plasma cells, and T cells in nasal polyps a repeated expression of RAG1 and RAG2 (recombination activation genes) can be revealed that are necessary for receptor revision [103]. Furthermore we were able to identify the up-regulation of activation-induced cytidine deaminase (AID), which is a factor indicating as well an active CSR and somatic hypermutation of immunoglobulins [104]. In CRSwNP, the concentrations of RAG1 and RAG2 mRNA is increased and correlates with the severity of the inflammation and the presence of Staph. aureus enterotoxin (superantigen)-specific IgE in the mucosa of nasal polyps. Those results prove a local receptor revision and the class switch to IgE and the differentiation of B cells to IgE secreting plasma cells in polypous tissue of CRSwNP without obligatory involvement of other lymphoid structures as for example lymph nodes. In tissue homogenates of CRSwNP the concentrations of important markers of Th2 induced inflammatory processes including IL-4 are significantly increased; IL-4 stimulated the synthesis of the ε-germ line transcript (GLT) that is used during CSR to IgE [103]. In CRSwNP, the concentrations of ε-GLT are significantly increased. The same is true for the B cell activating factor of the TNF family (BAFF) [105], which stimulates the development of follicles, and the B lymphocyte-induced maturation protein (BLIMP). Both BAFF and BLIMP are involved in the differentiation of B cells to plasma cells [106], [107]. Finally, we could reveal the presence of Iε-Cc class switch transcripts by means of gel electrophoresis and southern blotting and confirm it by sequencing of 339 bp long cDNA sequence, which unequivocally proves the local class switch in CRSwNP tissue [103]; a local IgE synthesis was previously shown in allergic rhinitis [108].

The proof for the local receptor revision was given by the up-regulation of RAG1 and RAG2 in B cells, plasma cells, and T cells. Indeed, the percentage of those cells that express RAG proteins in CRSwNP is similar to tonsillar B cells (15–26%) and significantly higher than in circulating B cells (<5%). Relevantly high percentages of B cells (20–30%) can also be found in target organs of autoimmune diseases. Recently it could be shown that both BAFF and the autoantibody are increased in nasal polyps and possibly play a role in the pathogenesis of CRSwNP [109].

Staph. aureus enterotoxin IgE was found in about 30% of CRSwNP patients, but not in the nasal mucosa of control groups. In the SE IgE positive polyps, the quantities of IgE, ECP, but also RAG1 and RAG2 were significantly increased than in SE IgE negative polyps which may be a hint to a direct stimulation of the RAGs by Staph. aureus. The correlation between RAG expression and a confirmed contact with Staph. aureus enterotoxins proves convincingly that reactions have been stimulated in the local germinal center and the polyclonal IgE expression by superallergenes [103]. We have already shown that local SE specific IgE directed against enterotoxins and polyclonal IgE resulting from the activation of plasma cells may contribute to the form and persistence of inflammation in CRSwNP; such IgE antibodies are active against several 100–1,000 different inhalative allergens and against allergens of Staph. aureus itself and cause a degranulation of mast cells after exposition [110]. Those results correspond to the fact that the treatment of CRSwNP with anti-IgE antibodies (Omalizumab) clearly reduces the size of the polyps and the symptoms of the disease (Figure 4 [Fig. 4], Table 3 [Tab. 3]).

2.3.3 Mast cells and eosinophilic granulocytes

Mast cells often occur in the nasal mucosa and have a physiologic function in the context of innate immune defense and wound healing. The activation of mast cells leads to the release of already present granules containing histamine, serotonin, proteoglycans, and serine proteases and to the de novo synthesis and release of different eicosanoids, chemokines, and cytokines. Prostaglandin D2 from mast cells was correlated with the recruiting and activation of Th2 lymphocytes in nasal polyps [86]. The stem cell factor (SCF) released from epithelial cells might substantially contribute to the recruiting of mast cells in nasal polyps [111]. In cases of allergies, the mast cell degranulation is initiated via an antigen-induced linkage of IgE molecules that are bound to highly affine receptors on the mast cell surface. However, there are other IgE-dependent and IgE-independent processes inducing, enhancing, and maintaining degranulation [112]. In particular, studies with explanted polyps have shown that a mast cell degranulation can also be triggered by other mechanisms including protein A (SpA), which is a surface protein of Staphylococcus [113]. Interestingly, it could not be definitely clarified if the number of mast cells in CRSwNP was increased in comparison to CRSsNP or control tissue [114]. Functional studies, however, allow the hypothesis that mast cells are much more active in nasal polyps and in vivo react more sensitively on external triggers [113]. With regard to the massive polyclonal IgE production, which is typical for CRSwNP, and to the possibility of direct activation of mast cells by means of special proteins of Staph. aureus, it is highly probable that in cases of CRSwNP a persisting activation of mast cells occurs. The inhibition of the continuous mast cell activation by innovative approaches might contribute to clarifying the significance of those cells in persisting inflammatory processes.

Eosinophils are circulating granulocytes that are responsible for immune defense at mucosal surfaces, primarily against multicellular parasites, but also for the remodeling and the repair of the mucosa. Their high amount in the mucosa of the airways in CRSwNP is associated by some authors with a certain origin of a disease, especially with the infection with fungal spores, however, there is still no final proof. The degree of eosinophilia in CRS is independent from the simultaneous presence of allergic rhinitis or fungal sinusitis which possibly allows concluding overlapping pathophysiological processes. In addition, the degree of tissue eosinophilia in CRSwNP correlates with the severity of the disease, the diagnosis of aspirin sensitivity, the occurrence of comorbid asthma [115], and the necessity of surgical revision [116]. At the same time, eosinophilia is not imperatively associated with CRSwNP; in 85% of the polyps of Asian patients as well as in about 15% of the polyps of Caucasian patients, the cellular pattern is not eosinophilic, but neutrophil. Instead of the expression of IL-5, IL-17 and IFN-γ are found as well as corresponding transcription factors [97].

For eosinophils, the chemokines RANTES, eotaxin 1-3, MCP 1-4 are relevant that are all mainly secreted by nasal epithelial cells and exercise their functions via the receptor CCr3 [117], [118], [119]. Also dendritic cells and macrophages may contribute to the production of eotaxin and other CCR3 ligands. The Th2 cytokines IL-4 and IL-13 play an important role in the induction of chemokines via STAT6 and NF-κβ. GM-CSF and IL-5 induce an enhanced migration and adhesion of eosinophils in the tissue of nasal polyps and favor the survival of those cells; IL-5 is an important priming and survival factor for eosinophils and antibodies against IL-5 induce the apoptosis of eosinophils in CRSwNP tissue [100], [120]. In summary, the process of recruiting, activation, and differentiation of eosinophils in CRSwNP is mainly promoted by Th2 cells and the cytokines released by them. There are sound hints that Staphylococcus superantigens favor eosinophilia in polypous tissue by enhancing the local release of Th2 cytokines by acting on the Th2 cells [99], [113], [115]. Recently, there were even hints that also Staphylococcus biofilms might favor eosinophilia in CRS independent from the polypous status or from super antigens [121]. The mechanism of this possible effect is unclear. Factors as for example IL-33, TSLP, and IL-25, which activate ILC2, might induce the production of IL-5 and thus influence the immune reaction in direction of a Th2 profile (Len Feng, unpublished data).

In the literature it is abundantly described that glucocorticosteroids can inhibit the recruiting, survival, and activation of eosinophils in CRS [122]. A recently performed double-blind trial with oral corticosteroids confirmed the clinical, however short-term, effectiveness on the nasal polyp score and the reduction of IL-5 and ECP in nasal secretion [123]. Both IL-5 and its soluble receptor are increased in eosinophilic nasal polyps [124]; this constellation locates the cells in the tissue. Studies with monoclonal antibodies against IL-5 showed a clear clinical effect while the amount of eosinophils in the blood and the mucosa significantly decreased after this kind of therapy [101].

Also neutrophils are circulating immune effector cells with well described functions in the early phase of defense, phagocytosis, and killing of extracellular microorganisms. In CRS, especially the chemokine IL-8 that is partly released from nasal epithelial cells as reaction on PAR-2 stimulation seems to trigger the recruiting of neutrophils [49]. The role of neutrophils in CRS is still unclear; in the mucosa of mucoviscidose patients, their amount is extremely increased together with the concentration of IL-17 [125].

In CRSsNP and CRSwNP, the degree of infiltration with neutrophils can be compared, in cases of cystic fibrosis it is much higher; in contrast, the infiltration with eosinophils is significantly higher in CRSwNP than in CRSsNP; each eosinophilic polyp also has a relevant number of neutrophils. Polyps of Chinese patients were non-eosinophilic or neutrophil in 85% of the cases [97]. However, this pattern may change so that the inflammation achieves a rather eosinophilic character in the course of time, accompanied by the presence of eosinophilic mediators, IgE and Staph. aureus in the mucosa [126].

2.3.4 Factors contributing to the resolution of inflammations (resolvins)

Not only inflammatory processes, but also their resolution are active processes where numerous lipid mediators are involved. The recently discovered inflammation resolving resolvines of the E and D series, protectins, and maresins have a strongly inhibiting effect on human cells. This is why those three mediator families and their acetylsalicylic acid triggered forms were called specialized pro-resolving factors (SPMs) [127]. Arachidonic acid (AA) and omega-3 fatty acid – the essential eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) – are substrates for the biosynthesis of highly inflammation inhibiting or inflammation resolving mediator substances. As it is a relatively young field of research requiring highly sophisticated measuring techniques, there is only little known about the presence and role of those SPMs in the upper airways. However, the pro-resolving mediator substance of lipoxin A4 originating from arachidonic acid has already been measured in patients with CRs [85]. Tissue of nasal polyps from the upper airways of CRSsNP and CRSwNP patients had higher concentrations of LXA4 than healthy nasal mucosa; in contrast, the LXA4 concentration in patients with aspirin sensitivity was relatively reduced in comparison to patients with nasal polyposis without such a sensitivity. Probably, the same pattern could be found in other SPMs: in order to reduce inflammation, the up-regulation of pro-resolving factors in the affected mucosa is induced; this process, however, seems to be disturbed in particularly severe types of inflammation such as NERD so that the inflammation may become persistent. The external substitution of pro-resolvins might be a possible therapeutic approach.

2.4 Remodeling of the mucosa of the paranasal sinuses

Cellular remodeling processes are dynamic processes where the production and degradation of the extracellular matrix (ECM) are balanced and regulated by different mediators among them TGF-β. TGF-β is considered as central factor in the remodeling process in the airways because it attracts fibroblasts, induces their proliferation and up-regulates ECM synthesis (e.g. of collagen). As already described, the protein concentrations of TGF-β1 and 2, the expression of mRNA of the TGF-β receptor (R) I and RIII and the number of activated cells with positivity for pSmad 2 (phosphorylated protein “mothers against decapentaplegic homolog”) (which is a sign for the activation of the cell by TGF-β) is significantly higher in patients with CRSsNP compared to control groups [21]. In CRSwNP patients the TGF-β1 protein concentration, the expression of TGF-β-RII and -RIII mRNA as well as the number of activated pSmad 2 positive cells were significantly lower than in control groups. Those data confirm a relevant difference between these two CRS subgroups with regard to the regulation of TGF-β and its signaling which manifests as a deficient collagen production in CRSwNP and as exceeding collage deposition in the ECM in CRSsNP. The TGF-β signaling also contributes to the regulation of metalloproteinases (MMP) and their natural tissue inhibitors (TIMP; tissue inhibitors of metalloproteinases). The overexpression of MMP7 and MMP9 without compensation by TIMP1 and TIMP4 is associated with a degradation of ECM, the development of vacuoles, and the deposit of albumin in nasal polyps, whereas the up-regulation of TIMP in CRSsNP inhibits edema [67]. Thus, CRSsNP may be characterized as fibrosis while CRSwNP is rather described as edema.

It might be presumed that the tissue remodeling is a consequence of the inflammation; this sequence could be brought in line with the high activation of TGF in the mucosa adjacent to the polyps and with the deposition of albumin in nasal polyps correlating with IL-5 [39]. More recent data, however, allow drawing the conclusion that remodeling precedes the inflammation at least in CRSsNP [128]. In a study where TGF-β and inflammatory cytokines were measured in the different paranasal sinuses of patients in an early stage of CRSsNP the protein concentrations of TGF-β1 were significantly up-regulated in the area of the osteomeatal complex, which is the central access to the paranasal sinuses, and were accompanied by an increased production and deposition of collagen in this area. Th1-regulated and inflammatory cytokines or myeloperoxidase protein as markers of activated neutrophils, however, were not up-regulated in these patients at that time. Those observations emphasize the central role of TGF-β and suggest that the remodeling in CRSsNP occurs independently from the inflammatory processes and precedes it (Figure 5 [Fig. 5] and Figure 6 [Fig. 6]).

2.5 Interaction between bacteria (microbiome) and immune defense

According to the current opinion, the detection of pathogenic germs on the nasal mucosa by swab means automatically disease of at least colonization that may lead to disease at any time. Frequently occurring germs of bacterial infections of the upper airways are germs like Staph. aureus, Hemophilus influenza, Pseudomonas aeruginosa, and Moraxella catharralis. Today it is well-known that the nasal mucosa is always, at any time in life, colonized with hundreds of different germs that – as far as their presence is balanced – guarantee a healthy condition. With the advent of the field of molecular biology, culture independent methods have been developed in order to examine microorganisms based on their genetic patterns. As a consequence, a clearly more complex flora was discovered in the upper airways than it had been suspected until that time. Due to the development of culture independent means it is meanwhile possible to identify species of microorganisms that could not be detected with previous growth methods. Today it is known that the human body is the home of 10–100 billions of microorganisms, an amount that is far higher than the number of body cells. The bacterial flora that has been known only for a short time is called human microbiome. Different regions of the body such as the nasal mucosa, skin, urogenital tract etc. have their own microbiomes encompassing ideally many microorganisms in relatively similar low frequencies (“richness, evenness”). If single germs disturb this balance by proliferation and by suppression of others, a pathologic situation occurs.

Based on the creation of comparing micriobiome profiles in a small cohort of CRS patients, on whom no further details were defined, and healthy test persons, it was assumed that the flora of the paranasal sinuses of CRS patients has a significantly lower multitude of bacteria compared to healthy controls. While on the one hand numerous phylogenetic distinct lactic acid bacteria were missing, on the other hand an increase of the relative incidence of a certain type of Corynebacterium tuberculostearicum was observed [129]. The authors drew the conclusion that this germ could be made responsible for the pathogenesis of CRS; for confirmation of its pathogenic role of a certain microbiome constellation in a specific inflammation status, however, multicentric studies in large, well defined CRS populations are required [130]. Additionally, the relationship between microbiome and immune defense in the mucosa could be bidirectional, i.e. the bacteria exercise a certain pressure while on the side of the host an insufficient defense is present, for example because of alternatively activated macrophages, that show a reduced phagocytosis and an insufficient killing of intracellular germs [93]. Scientific examinations on how certain germs influence the immune reaction of the mucosa of the nose and paranasal sinuses, could shed new light on the pathophysiology of CRS and lead to new treatment approaches. The manipulation of the flora or the introduction of specific healthy germs (e.g. lactic acid bacteria) might turn out to be helpful for the treatment of inflammatory diseases and break the dominance of certain germs such as for example Staph. aureus or Pseudomonas aeruginosa.

2.5.1 Interaction between viruses and bacteria

Common colds rank among the most frequently occurring infectious diseases of humans and are mainly caused by human rhinoviruses, the respiratory syncytial virus (RSV) as well as corona, adeno, and parainfluenza viruses. An adult suffers about 2–5 times per year under colds while the rates of infections in females aged between 20 and 34 years are higher, probably because of infection by their children. Children have 6–8 common colds per year, day care institutions for children represent a relevant risk factor for diseases of the airways in children and their mothers. Because of the fact that certain viruses appear seasonally, a clear dependence from the seasons is observed with higher incidences in fall and winter [131].

Typical initial symptom of a common cold is a sore throat because the virus preferably binds via the intercellular adhesion molecule 1 (ICAM-1) to the tissue of the nasopharynx/lymph, subsequent nasal symptoms are sneezing, nasal secretion of fluid or mucus (rhinorrhea), and nasal obstruction. The infection can extend via the Eustachian tube to the middle ear or via the trachea into the lower airways so that coughing and bronchitis occur. After 10–14 days the symptoms regress spontaneously if no acute postviral rhinosinusitis occurs [1].

Viral infections of the nasal cavity are the most common reason of acute asthma exacerbation in children (80–85% of asthma exacerbations) [132] and in adults (about 80% of asthma exacerbations) [133]. In two third of the cases with proven virus, rhinoviruses are detected. In asthmatics, the up-regulation of ICAM-1 on epithelial cells, a receptor that is used by 90% of the rhinoviruses, might be responsible for the higher sensitivity especially of atopic patients with more frequent infections and more severe and longer lasting symptoms [134]. In vitro studies reveal that rhinoviruses replicate more efficiently in primary bronchial epithelial cells of asthmatics than healthy people. There is a strong correlation between the virus charge and the severity of the symptoms in the lower airways and an increase of the bronchial hyperactivity. In association to the pathogenesis or rhinovirus induced asthma exacerbations, impaired Th1 reactions (IFN-γ and IL-12), that seem to have mainly a protective effect against the replication of viruses, and enhanced Th2 reactions (IL-4, IL-5, and IL-13) are described as origin of more relevant virus-induced asthma symptoms [135].

In adults suffering from mild/moderately severe atopic asthma and in bronchial epithelial cells of children with severe therapy-refractory atopic asthma, a defective induction of type-1 interferon (IFN-β) and type-III interferon (IFN-λ) was found [136]. Actually, patients with severe therapy-refractory asthma had an increased virus replication that correlated negatively with the amount of interferon mRNA. Also a study performed with asthmatic children living in cities revealed that the treatment with antibodies against immunoglobulin E (IgE) could improve the control of asthma, reduce the need of asthma medications, and nearly eliminate the seasonal peaks of exacerbations induced by virus infections [137]. This would mean that the reduced Th1 immune reactions might be based at least partly on an enhanced Th2 immune response.

Actually, unpublished results show that also tissue of nasal polyps in the ex vivo mucosal model respond insufficiently to herpes simplex virus (HSV1) and rhino virus infections; a deficient IFN-γ production and IL-17 release as well as an increased release of TNF-α were the main characteristics of mucosal reaction on a virus infection in CRSwNP with Th2 polarization in comparison to healthy inferior turbinates (Lan Feng, in press). This deficient virus defense could lead to another phenomenon: as virus infections open the doors to bacteria and allow them entering into the mucosa despite an otherwise intact epithelial barrier [138], the probability of bacterial ingress, such as for example Staph. aureus, could be increased in cases of frequent virus infections. Because of the fact that an alternative activation of macrophages occurs in a Th2 polarized environment (IL-5 plus CRSwNP), the intruders could avoid the defense mechanisms of the mucosa in such a situation and colonize the mucosa without being phagocytized or killed by macrophages [93] (Figure 7 [Fig. 7]).

2.5.2 The role of Staphylococcus aureus as amplificator of the inflammation

Staph. aureus colonizes the nose very frequently; about one third of all Europeans are life-long carriers of coagulase positive Staph. aureus. Especially in CRSwNP [69] Staph. aureus colonizes the middle nasal meatus and the surface of the nasal polyps. The colonization rates are very high with 67 and 87% of the patients with CRSwNP and asthma or NERD, respectively. Staph. aureus does not only colonize the mucosa but produces biofilms adhering at the inflamed and damaged mucosa in order to serve as reservoir for planktonic germs. Every now and again single germs are released from the biofilms that protect, inform, and nourish germs as three-dimensional structures. Those germs re-infect the mucosa [121]. By means of PNA-FISH (a peptide nucleic acid fluorescence in situ hybridization technique) intramucosal Staph. aureus can be identified very specifically that is found intracellularly only the tissue of CRSwNP patients [139]. The germ can also be present as “small colony variant”, a sleeping variant with low metabolism, or replicate in epithelial cells of nasal polyps [140]. Those findings confirm the persisting character of Staph. aureus infection and indicate its possible role as amplificator of inflammations by means of its immune proteome; beside the superantigens, Staph. aureus produces a multitude of proteins that may have an impact on the human immune system.

Manipulation of the immune system means advantages for the germs. We could show that the Th2 inflammation of the nasal polyps favors the alternative activation of macrophages to so-called M2 macrophages while those immune cells are characterized by a reduced phagocytosis and intracellular killing of germs including Staph. aureus compared to the usually favored M1 macrophages [93]. This deficiency of the mucosal defense allow Staph. aureus to colonize the mucosa and to enhance the Th2 immune reaction via different mechanisms.

Staph. aureus synthesizes and secretes numerous immune proteins and enterotoxins, among those the classical enterotoxins (SEs) SEA, SEB, SEC, SED, SEE, and toxic shock syndrome toxin-1 (TSST-1) [141]. SEs, also known as superantigens, are able to activate T cells via an antigen-unspecific binding to the variable β chain of the T cell receptor which again allows a polyclonal activation of a high number of T cells with different characterization; up to 20% of the local T cells can be activated at the same time instead of the usual rate of less than 0.1% which may cause a “cytokine storm” [142]. This cytokine storm can lead to the sudden death of the patient, and in cases of chronic triggering it maintains a severe persisting inflammatory reaction within the tissue. Furthermore, SEs can activate B cells, eosinophils, epithelial cells and other cell populations which enhances the immune globulin synthesis including IgE and the migration of eosinophilic granulocytes in the tissue. The result is a further Th2 polarization; SE-IgE positive nasal polyps have a manifold increased IgE, ECP, and IL-5 compared to SE-IgE negative polyps. Recently, we were able to provide the proof of the local release of SEs and other immune proteins from Staph. aureus in the tissue of nasal polyps by means of proteomics (unpublished data). The changes of the innate and adaptive immune response induced by SEs [143] promote the survival of Staph. aureus. In an animal model, SEs cannot only enhance Th2 mediated inflammations of the airways but also induce them [144], [145]. The intranasal application of allergens in mice normally leads to development of tolerance; the addition of SEB, however, leads to sensitization and formation of an eosinophilic inflammation reaction of the upper and lower airways [146]. We could show in human mucosa that protein A and SEB from Staph. aureus lead to a significant degranulation of mast cells and to the activation of Th2 cells with consecutive release of the Th2 cytokines IL-4, IL-5, and IL-13 [113]. These effects further influence the T cell response in direction to Th2 and thus contribute to a persisting, in particular eosinophilic inflammation of the airways. Furthermore, SEB induces the release of chemokines from epithelial cells which leads to the migration of granulocytes and their activation [147].

Recently, we could also prove that actually intramucosal Staphylococcus germs amplify the production of IL-5 in nasal polyps; after killing by antibiotics or Staphylococcus-specific bacteriophages, the spontaneous IL-5 production significantly reduced to the level of the polyps that were not colonized by Staph. aureus (Bachert, in press).

However, most important is the ability of staphylococcal products like SEA and protein A to stimulate the production of IgE antibodies [148], [149]. This B-cell stimulation and transformation to plasma cells can also be observed in tissue of nasal polyps [150]; in this context accumulation of very high concentrations of IgE in the tissue results while more than 5,000 kU/l IgE were measured in the tissue of nasal polyps [102]. A real local IgE synthesis in polyps may be organized via the formation of follicle-like structure in the nasal polyp and the expression of a series of mediators, that are important for immunoglobulin synthesis, such as AID (activation-induced cytidine deaminase) and BAFF, while the class switch of IgG to IgE and the synthesis of specific IgE antibodies do not require further lymphatic structures like lymph nodes [104], [115], [151]. Recent examinations confirm this hypothesis of a local immunoglobulin synthesis triggered by SEs based on the proof of SE-IgE associated expression of RAG1 and RAG2 [103].

Specific antibodies in polypous tissue are only a small part (mostly less than 2%) of the total IgE which can only hardly be identified or not identified at all. Nonetheless, this polyclonal IgE is functional. According to the presence of specific IgE antibodies in the tissue, as mast cell degranulation can be triggered by exposure to the corresponding allergen, independent from the presence of the IgE antibody in the serum [110]. This means that skin tests or serum IgE measurements may be negative and nonetheless a local degranulation of mast cells is triggered by allergen contact; the IgE of nasal polyps can be transferred to basophiles and also there it triggers a specific activation of the basophiles (RBL SX38 cells) in tests. This means the proof of the functionality of local polyclonal IgE [110] and these observations can also be transferred to the lower airways (Figure 8 [Fig. 8]).

2.6 From sinusitis to asthma

Around 40% of our patients with nasal polyposis also suffer from asthma. The relation between CRS and asthma has recently been proven for Europe in a multi-centric study of the GALEN group [6]. This association applies to the so-called late-onset asthma, however, the patients are mostly not allergic. In a study on the definition of biochemical factors in the tissue of nasal polyps associated with an increased risk for comorbid asthma within the group of CRSwNP patients, it could be observed that IL-5, IgE, and SE-IgE predict asthma. If SE-IgE is present together with a high total IgE, the risk of comorbid asthma is multiplied compared to SE-IgE negative CRSwNP patients [99]. This observation could recently be confirmed in an independent cluster analysis. Two of 10 CRS clusters were SE-IgE positive and had a rate of comorbid asthma of 65–75% in contrast to CRs patients whose comorbidity was less than 10% (Tomassen, in press). Eosinophil but SE-IgE negative CRSwNP patients suffer from asthma in 20–40% of the cases.

Also in patients with severe asthma, independent from the diagnosis of polyposis, SE-IgE positivity is found significantly more often (60%) than in control groups (13.0%, P<0.001) [152]. A logistic regression analysis showed a significantly higher risk of each type of asthma in SE-IgE positive patients (OR 7.2 [95% confidence interval (CI) 2.7–19.1] or of severe asthma (OR 11.1 (95% CI 4.1–29.6)) in comparison to serum SE-IgE negative patients. According to skin test and serum IgE, 21% of the patients with severe asthma were non-atopic on inhalative allergens; thus SE- IgE is a factor of “intrinsic” asthma independent from an atopia. The application of oral corticosteroids, the number of hospitalizations because of acute deterioration of the asthma, and the lung function parameter FEV in 1% were all associated with SE-IgE in the serum [152]. So we assume that Staph. aureus plays a major role in the pathophysiology of severe asthma and SE-IgE in the serum marks the involvement of the germ in the disease.

The sensitization against Staph. aureus enterotoxins is rather frequent in Europe with a prevalence of nearly 30%. For the first time, this evaluation proved in a large epidemiologic study performed in the population of the EU that SE-IgE is clearly associated with asthma [153]. The results have recently been confirmed by a Korean study group [154]. Another study performed in 240 older patients with asthma (onset of the disease ≥40 years), however, showed that the SE-IgE concentration in the serum of the patients was significantly higher than in control groups. Furthermore, SE-IgE correlated with the total IgE, the eosinophilia in the sputum, with the severity of the asthma, and the diagnosis of CRS (Song, in press). The observations emphasize the role of SE-IgE in non-atopic asthmatics with late onset and indicate the significance of CRSwNP in this patient population.

Even in children and adolescents, associations between SE-IgE and asthma were found, but in this age group they are less important than in allergic diseases [155], [156] (Sintobin, in press).

2.7 Biomechanisms of recurrences after surgery

In the same way as concomitant asthma, also the probability of recurrences after total surgical removal might be calculated from biopsies of CRSwNP patients. The claim of completeness is based on the fact that in every polyp an immunological memory is saved in the form of so-called memory cells that maintain the existing immune reaction unless they are surgically removed during an intervention. Surgeries of recurrences in CRSwNP are frequently performed. A follow-up examination over 12 years performed in Ghent, Belgium, revealed recurrences in nearly 80% of the patients requiring at least intensive drug therapy (Gevaert, in press). A total of 36% of the patients underwent at least one revision surgery while the second interventions were performed over all 12 years. Corticosteroid resistant recurrences may even develop 10 years after the first surgical intervention.

In a study performed over a shorter interval of 7 years, we examined the immune profiles that were associated with recurrences [9]. Biopsies of CRSwNP patients who had developed a recurrence within this time were compared to biopsies of patients who had not recurrence within this same period of time. In all specimens the following parameters were measures: Th1, Th2, and Th17 cytokines, IgE, pro-inflammatory cytokines and mediators of eosinophilic (ECP) and neutrophil inflammation (MPO). Patients with recurrences had significantly higher concentrations of total IgE, SE-IgE, ECP, and IL-5 (OR 6.4) at first surgery, whereas IFN-γ was significantly reduced (OR 0.047). The concentrations of IL-17, IL-6, TGF-β1, and IL-1β did not differ between the groups. Asthma and NERD, both Th2 weighted, as clinical parameters were also more frequent in the group of recurrences.

The conclusion can be drawn that the polypous tissue of patients with high risk of recurrences is different from tissue with low risk for recurrence. The immune profile that has to be antagonized can be deducted, and the prognosis of the individual patient can be estimated. Those findings show as well as observations of comorbid asthma how heterogeneous chronic rhinosinusitis is and which great influence is exercised by T helper cells on the disease, their therapy, and prognosis. So we have to move away from the idea that a simple classification into CRSsNP and CRSwNP meets the differentiation of CRS. Beside endoscope and computed tomography we will have to introduce biomarkers into the diagnostic concepts in order to meet the individual requirements in the sense of personalized medicine.

This development has only started. It might be expected that a better knowledge of the pathophysiology does not only contribute to better predict the patients’ prognosis but allows more targeted application of therapeutic options. While a CRS patient with severe fibrosis and moderate neutrophil inflammation may be treated sufficiently long-term with only one rather limited minimally invasive intervention, the treatment of a patient with severe Th2 associated inflammation and significant edema will be directed at removing the whole tissue of the nasal polyposis. This patients would then undergo a much more aggressive and frequent follow-up as well as long-term application of topic glukocorticosteroids, among others, while the CRS patient might have experienced complete healing after three months. For the first time we can offer biomarkers, however, only in the tissue, later certainly also in the serum that also allow to identify those patients already before first surgery who would have to better undergo drug therapy with humanized monoclonal antibodies and other alternatives to be developed instead of surgery.

This perspective will be further developed in the following chapters while only the differentiation in clusters and then their individual treatment modalities will be discussed.


3 Cluster analysis of CRS: definition for CRS endotypes

Nowadays, statistical methods allow examining similar disease patterns by analyzing certain clinical or biomedical characteristics. This approach is called cluster analysis that under optimal conditions is independent from the examiner. However, this method is already limited by the fact that a certain choice of characteristics is made for the analysis. The cluster analysis has promoted the differentiation of severe asthma and it could show that asthma has many different phenotypes [7] that have to be treated in differentiated ways.

In the context of a European project called GALEN we have collected the data of several hundreds of CRS patients. From a subgroup of patients (169 CRS and 89 healthy persons) we analyzed the tissue taken from the paranasal sinuses. The analysis encompassed parameters from the field of remodeling, proinflammatory cytokines, T cell cytokines for Th1, Th2, and Th17 lymphocytes, markers of eosinophilic and neutrophil activation as well as IgE and SE-IgE. In this hierarchic cluster analysis, that was uninfluenced apart from that, exclusively tissue markers were included. It was the objective to recognize clusters of CRS based on biological patterns (Tomassen, in press). Only in a second step, the clinical parameters were considered in order to verify the defined clusters regarding their clinical relevance.

The following aspects could be identified: CRS can be divided into 10 clusters that partly have overlapping characteristics. The markers IgE, ECP, IL-5, SE-IgE, and albumin are relevantly associated with each other, the same is true for the markers IL-1, IL-8, and MPO. Thus there is already a separation of neutrophil from eosinophilic inflammations. However, it becomes obvious that in every eosinophilic nasal polyp regularly also neutrophil inflammation is found. In addition, the results show that albumin might be the connective link between eosinophilic inflammation and edema in nasal polyposis while neutrophil inflammation did not correlate with albumin. A total of 6 of 10 clusters was characterized by an eosinophilic and 8 by a neutrophil inflammation. Two of the clusters were only neutrophil and two had no clear inflammatory pattern. This phenomenon is interesting because it shows that CRS may be present even without evident inflammation. Additionally, single clusters revealed increased TNF-α, IFN-γ, or IL-17 concentrations that were usually associated with neutrophil inflammations. Two of those 6 clusters (cluster 9 and 10) with eosinophilic inflammation were SE-IgE positive and had increased IL-5, IgE, and albumin levels in comparison to SE-IgE negative clusters.

How can those clusters have a clinical relevance? Figure 9 [Fig. 9] shows the polypous part within each cluster on the left side, while both non-inflammatory clusters were mainly defined as CRSsNP and both IgE positive clusters as CRSwNP according to clinical criteria. In the 6 clusters with eosinophilic inflammation, at least 60% of the cases had been assessed as CRSwNP. On the right side of the figure, the part of comorbid asthma in the patients of the single clusters is depicted. Whereas patients in clusters 1–4 had comorbid asthma in less than 20% of the cases, this percentage in the clusters 9 and 10 is rather high which shows the clinical relevance of the clusters.

Now, the endotypes can be deducted from the cluster analysis that follow certain pathophysiological principles and thus also the same group of therapeutics may be applied, e.g. corticosteroids, but also biologic drugs.

Those endotypes are defined in Table 4 [Tab. 4]. It becomes obvious that the eosinophilic endotypes are associated with polyposis and comorbid asthma; however, those characteristics are even clearer in the SE-IgE positive endotype. Parallel, also the risk of recurrence after surgery increases; also in this context the markers of Th2 inflammation as well as the total IgE and SE-IgE that are associated with the incidence of recurrences. Finally, there are only the eosinophilic – mainly the strongly eosinophilic/SE-IgE positive endotype that can be treated by application of innovative therapeutic approaches or biologic drugs that will be discussed later on. So these CRS endotypes have a high clinical relevance and can be used for the prognosis after surgery, prognosis of asthma, and finally prognosis of therapeutic response to targeted biologic drugs. This approach is the base for personalized medicine in the management of CRS.

3.1 Special phenotypes

3.1.1 Allergic fungal sinusitis (AFS)

Because of the fact that fungal spores are omnipresent, they permanently enter in the airways by breathing and are deposited on the mucosa. In isolates, Aspergillus, Penicillium, Cladosporium, Candida, Aureobasidium, and Alternaria are found most frequently. In the airways of healthy people, they rarely become pathogenous, however, sometimes they are able to cause diseases. The non-invasive type of mycotic CRS (fungus ball and allergic fungal sinusitis) are diagnosed more frequently than invasive types [157], [158]. In geographic areas with warmer climate, the prevalence of allergic fungal sinusitis is higher; the presence of fungi such as Bipolaris spicifera, Curvularia lunata, or Aspergillus species in the paranasal sinuses is typical for the disease [158]. A high total IgE concentration and a relevant eosinophilia in the blood and the mucosal tissue are observed. In contrast, it is unclear how those fungi induce this high IgE concentration because they do not release stimulants for such IgE production, as for example superantigens. More recent data reveal the co-existence of the fungus Aspergillus fumigatus with Staph. aureus in biofilms in patients coming from Saudi Arabia while Staph. aureus is able to trigger the polyclonal IgE production and the severe inflammatory reaction [159]. This observation was confirmed in cases of ABPA (allergic broncho-pulmonary aspergillosis), which is the equivalent of allergic fungal diseases of the paranasal sinuses in the lower airways, by the evidence of SE-IgE antibodies and their correlation with the total IgE (L. Chishimba, Manchester, in cooperation with our lab; publication is prepared). Those observations could lead to a new understanding of AFS and ABPA and thus to a new therapeutic approach of Staph. aureus and fungal germs (Figure 10 [Fig. 10]).

3.1.2 Aspirin sensitivity (NERD)

Often an intolerance against aspirin or non-steroidal anti-inflammatory drugs (NSAID) is observed in patients suffering from severe polyposis and asthma. The prevalence of NERD (non-steroidal drug exacerbated respiratory disease) amounts to around 8% in the group of CRSwNP and so it is significantly higher than in controls or CRSsNP. More than 50% of the patients with asthma and aspirin sensitivity also have polyps. NERD often develops as final diagnosis, i.e. after persisting rhinitis in the third decade, followed by asthma, nasal polyposis, finally aspirin intolerance occurs. About half of the patients suffer from severe asthma depending from steroids. Surgery of the paranasal sinuses is associated with a high incidence of recurrences in aspirin-sensitive patients [9], [160].

In diseases of the paranasal sinuses, especially in CRSwNP and NERD, the eicosanoid biosynthesis is modified. The imbalance is mainly characterized by an overexpression of proinflammatory mediators, i.e. of leukotriene, and by a deficit of anti-inflammatory mediators (prostaglandin E2 (PGE2) and lipoxin LXA4). Cysteinyl leukotrienes (cys-LT) are important inductors of airway inflammations [85], [161], [162]. In CRSwNP/NERD the concentrations of those mediators, of enzymes contributing to their biosynthesis (leukotriene synthase, LTC4S, and 5-lipoxagenase, ALOX5) and their receptors are significantly higher in comparison to CRSsNP and control persons. They correlate with the number of activated eosinophils and the concentrations of ECP, IL-5, and IL-5Rα [85]. Furthermore, the ability of tissue of nasal polyps to produce PGE2 and to up-regulate cyclooxygenases (COX)-1, COX-2, and the prostaglandin E receptors EP2 is reduced under proinflammatory conditions [163]. The expression of transcripts of prostaglandin E receptors EP1 and EP3 is down- and the receptors EP2 and EP4 are up-regulated [164]. As the PGE2 concentrations are reduced, the synthesis of leukotrienes (LT) is no longer suppressed so that excessively many eosinophils and high quantities of cys-LT are found [85]. PGE2 could also influence remodeling of nasal tissue induced by fibroblasts [165]. Fibroblasts from nasal polyps produce significantly higher quantities of constitutively expressed COX-2 mRNA than fibroblasts of the inferior turbinates which stimulated vascular dilatation and mucin production [163].

The hematopoietic prostaglandin D synthase (hPGDS) and the microsomal prostaglandin E synthase 1 (m-PGES-1) are both involved in the biosynthesis of PGD2, however, they seem to be regulated otherwise in CRS [166]. The expression pattern of PGD2 receptors such as DP1 (D-prostanoid receptor 1) and CRTH2 (chemoattractant receptor homologous molecule) that is expressed on T helper cells of type 2, is not yet clarified: in CRSwNP the DP1 receptors is found mainly on tissue infiltrating, inflammatory, and constitutive cells while CRTH2 is mostly expressed in inflammatory cells (eosinophils and T cells) [167]. In tissue of nasal polyps, the de novo synthesis of PGD2 after stimulation via IgE is significantly up-regulated [113], and this release promotes the release the migration of Th2 cells via a CRTH2-dependent mechanism [86].

As can be read in recent studies, the progression of inflammation in NERD airway diseases is associated with a comparably reduced lipoxin synthesis while the mRNA expression of ALOX15 and the consecutive LXA4 concentrations in CRSwNP patients is up-regulated [85]. ALOX15 is increased in the epithelium and subepithelium and correlates positively with the number of activated eosinophils infiltrating the mucosa of the nasal polyps; NERD patients have a reduced basal synthesis and reduced ability to synthesize LXA4 under proinflammatory circumstances [85], [168].


4 Pharmaco-therapy of chronic rhinosinusitis

The options that are currently recommended for therapy of chronic rhinosinusitis (CRS) are summarized in international and national guidelines. Most wide-spread are the EPOS guidelines that have been established by an international team of experts (including myself) according to criteria of evidence-based medicine [1]. Among those treatment recommendations, topical and systemic glukocorticosteroids, antibiotics as long-term therapy or in cases of exacerbations as well as irrigations with saline solution are found. If those options do not lead to successful treatment or control of the symptoms, generally surgery is discussed. Postoperatively the same pharmacotherapeutics are continued or applied. The recommendations of the EPOS guidelines are summarized in Table 5 [Tab. 5] and Table 6 [Tab. 6] for CRS without nasal polyposis (CRSsNP) and CRS with nasal polyposis (CRSwNP). They can be completely downloaded via internet (http://www.rhinologyjournal.com).

4.1 Chronic rhinosinusitis without nasal polyps (CRSsNP)

Beside topical corticosteroids that are less effective in CRSsNP before surgery because of the eosinophilic character and the poor accessibility of the paranasal sinuses compared to CRSwNP, especially macrolides can be discussed as low-dose long-term therapeutics (>12 weeks) in CRSsNP. Even if the EPOS guidelines actually recommend macrolides unless IgE is not elevated in the serum, an extensive European study with azithromycin was negative [169]. However, there was criticism about the patient selection (CRSsNP and CRSwNP) and the missing consideration of serum IgE. A. Cervin who was very committed to macrolide therapy summarized 30 years of experience with microlides and many open studies in a recent review article that only two randomized controlled studies had been performed that contradict regarding their results. In one study that treated only CRSsNP patients with roxithromycin versus placebo a positive clinical effect was observed after 12 weeks of treatment. However, recently major concern have arisen in the context of macrolides as they might cause cardiac arrhythmia [170]. In patients with risk factors such as a prolonged QT intervals, bradycardia, hypokalemia, hypomagnesaemia etc. a long-term application of macrolides cannot be recommended. Macrolides may also interact with the cytochrome P450 system, cause ototoxicity, and finally lead to development of resistances to macrolide antibiotics in case of broad application [171].

4.2 Chronic rhinosinusitis with nasal polyps (CRSwNP)

The application of topical corticosteroids is not disputed in nasal polyps, as initial but also as postoperative therapy. A dosage of 2x daily has to be observed which can be reduced to 1x daily if reasonable when the disease is controlled (for example no recurrence or no exacerbation over at least one year after surgery). Because of the necessity of high dosage over several years, substances with a low bioavailability should be preferred; according recommendations are included in a therapeutic index [172]. In particular after surgery topical corticosteroid as drops are recommended. They are applied in a position with the head bent over or in the so-called Mecca position in order to distribute optimally in the ethmoid region and at the skull base. Recurrent polyps would preferably develop in these regions.

The effectiveness of doxycycline (100 mg/d) has been proven in a study of patients suffering from nasal polyposis over 20 days [123]. In this study, the effect of oral corticosteroid therapy on symptoms, objective clinical as well as biochemical parameters was compared to the one of doxycycline. A placebo group was also created. In this double blind randomized placebo-controlled study 47 patients with bilateral nasal polyposis either underwent therapy with methyl-prednisolone in decreasing dosage (from 32 to 16 to 8 mg every 5 days) or doxycycline or placebo therapy (200 mg on the first day). The patients were monitored over 12 weeks by means of peak flow measurements, endoscopy, symptom scores, and biomarkers in nasal secretion and peripheral blood. It became obvious that methyl-prednisolone and doxycycline caused a significant reduction of the size of the polyps compared to placebo. The effect of methyl-prednisolone was maximal after 2 weeks but before the end of therapy it already decreased and in total it was only significantly different of placebo over 8 weeks. The effect of doxycycline was less relevant but significant over the 12 weeks of evaluation. Methyl-prednisolone significantly suppressed the mediators ECP, IL-5, and IgE in nasal secretion while doxycycline reduced the concentrations of MPO, ECP, and MMP-9.

We drew the conclusion of this study that an oral corticosteroid application has only a relatively short effect on CRSwNP and that the side effects – especially in cases of repeated application – are outweighed. In practice we avoid oral corticosteroids as far as possible, in particular directly preoperatively because the blood eosinophils show a clear rebound effect after treatment. A high number of circulating eosinophils a few weeks after surgery must be considered as prognostically unfavorable.

Because of its positive effect on bacterial colonization including Staph. aureus and biofilm formation as well as because of reduction of MMPs (which contribute to the development of edema in nasal polyposis) and IgE, doxycycline is applied as long-term therapy for several weeks, especially in the postoperative phase in order to reduce edema and scar formation. The recommendations of the ENT Department of Ghent are summarized in Table 7 [Tab. 7].

It is obvious that those therapeutic principles are insufficient in some patients; even if a temporary improvement of the complaints can be achieved it cannot be maintained over a longer period of time. Especially in patients with CRSwNP pharmacotherapy is often not sufficient so that surgery becomes necessary. Recurrences occur frequently even after surgery so that some of the patients have to undergo surgery several times in their lives. A follow-up evaluation performed at the University of Ghent in 42 patients older than 12 years estimated the recurrence rate over 12 years with more than 75% while a total of 36% of the patients had to undergo at least a second intervention (Gevaert, in press). Another study from Ghent had identified biomarkers previously that in the case of necessary second intervention had already been increased at the time of first surgery in comparison to patients who did not need second surgery (here over 7 years): IgE, SE-IgE, ECP, and IL-5 [9]. Those markers can all be classified into the Th2 pattern. A high interferon level (IFN-γ, Th1 cytokine) could be measured in patients who did not require revision surgery. This suggests perspectives for a prognosis based on the biomarkers measured at the occasion of the initial intervention. Furthermore, it seems to be reasonable to apply therapeutics that are effective for eosinophilic inflammations, in particular glucocorticosteroids, in this patient population rather long and in higher doses. Additionally accompanying measures against Staph. aureus increase the control of the inflammation, for example by application of doxycycline or mupirocin.

For patients who underwent complete resection with the objective of the inflammatory tissue, who were treated postoperatively with the above-mentioned therapeutics, and who nonetheless had developed recurrences indicating surgery, the current treatment options are apparently insufficient. Innovative approaches, actually in particular so-called biologics, have to be considered. Regarding this development, we are currently only at the beginning. Currently only one humanized antibody is at our disposition limited to patients with the indication of severe allergic asthma that cannot be treated otherwise. In the near future, however, it might become obvious that those patients can already be identified before initial surgery by determining biomarkers and – as surgery will most probably not lead to the control of the disease – alternative therapy can be initiated immediately. Those reflections have to be made also with regard to the background of cost and benefit/risk analyses.

4.2.1 Specific reflections on allergic fungal sinusitis (AFS)

Treatment starts with the complete resection of fungal masses and colonized Staphylococcus as well as the polypous mucosa from the paranasal sinuses. Attention must be paid to complete removal and intensive postoperative care like in other eosinophilic polyps. Just as eosinophilic nasal polyps, the disease is also characterized by a Th2 pattern; IL-5 is much increased such as IgE, there are numerous secreting plasma cells and activated T cell that apparently dispose of a memory for specific antigens. The postoperative application of oral and topical corticosteroids supports the reduction and termination of the immune response.

4.2.2 Specific reflections on aspirin sensitivity (NERD)

Also nasal polyps in aspirin sensitivity or NSAID exacerbated respiratory diseases show a clear Th2 pattern where the markers of eosinophilic inflammation (IL-5, ECP etc.) and also the tissue IgE are very high [173]. SE-IgE is generally positive in the tissue and in cases of asthma also in the serum. In comparison to normal polyposis with asthma, a deficient production of LXA4 is obvious which has anti-inflammatory activity. Apart from that, surgery as well as conservative therapy of CRSwNP in NERD follow the same principles as described above (treatment scheme of Ghent, Table 7 [Tab. 7]). Also the application of omalizumab is not excluded.

Advocates of an adaptive deactivation must accept the reply that only few centers perform provocation with aspirin or lysine aspirin which is a precondition of adaptive deactivation; that a series of contraindications of provocation must be observed [174]; that the benefit of this therapy, especially postoperatively, is not proven; and that there are very contradictory ideas on effective but well tolerable dosage of aspirin [174].


5 Biologics for the treatment of asthma and chronic rhinosinusitis

It is clear that the pharmaceutical industry has experienced an unparalleled development of pharmacologically active peptide- and protein-based treatment approaches for therapy of different diseases of the mucosa of the airways and the gastrointestinal tract as well as systemic diseases (for example Crohn’s disease, multiple sclerosis, rheumatoid arthritis, just to mention some of them) during the last years. The development of such biological substances requires profound knowledge of specific molecules of which the binding or “deactivation” has a relevant therapeutic effect. Only then it makes sense to develop antibodies and to humanize them secondarily, i.e. to approximate them to the human antibody product as near as possible. This process is incomparably expensive in relation to the development of classic drugs. Currently about 200 biologics are used for patients, further 400 are tested in studies. Among the indications, also severe asthma is found that is very similar to chronic rhinosinusitis regarding its immune mechanisms, especially to the Th2 pattern of CRSwNP.

Different innovative biologics are tested in clinical studies for severe asthma and up to now finally one has been approved. Omalizumab is applied today in a relatively specific small group of patients with severe asthma, which cannot be treated otherwise, under strict conditions. One of the preconditions is that standard therapy with corticosteroids in high doses is not sufficient, that perennial asthma is present, and that a lung specialist confirms the indication of omalizumab. Omalizumab is a humanized monoclonal antibody that is targeted against fee IgE. It was primarily developed as antiallergic agent [175]. Meanwhile studies show that omalizumab is also effective without the presence of allergy in cases of severe asthma (the so-called intrinsic asthma) while those patients also have increased IgE serum levels (see above) that are not targeted against inhalative allergens. Insofar the limitations of the authorities regarding the application of omalizumab are already obsolete.

Also for chronic rhinosinusitis the single state-of-the-art studies (DBRPC) with biologics have been performed, up to now always in Ghent (Coordinating investigator: Claus Bachert); reports on the experiences with omalizumab have also been made by other departments. Among the tested humanized antibodies, also anti-IgE (omalizumab), anti-IL-5 (reslizumab and mepolizumab) as well as anti-IL-4/13 (dupilumab) can be found. The target molecules were targeted against Th2 associated mediators each. The studies reveal that the mentioned biologics are therapeutically effective in 60-80% of the patients. In the future, biomarkers shall help to increase this response rate. Without any doubt, the studies can also be valued as proof-of-concept for the possibility of targeted therapy of Th2 associated mediators in cases of eosinophilic chronic rhinosinusitis with nasal polyps with or without concomitant asthma.

Table 8 [Tab. 8] and Table 9 [Tab. 9] give an overview of possible target molecules for the treatment of Th2 associated respiratory diseases (CRSwNP and asthma) according to the literature available today.

5.1 Anti-IgE (Omalizumab)

The discovery of high concentrations of IgE in nasal polyps [115], [176] and the understanding that those IgE antibodies are polyclonal and still functional [110], has justified a therapeutic attempt with omalizumab, a humanized monoclonal antibody against free IgE. After positive reports on single cases [177], the first smaller DBPCR study with omalizumab in chronic rhinosinusitis, however, had negative results; the reason was probably that patient selection was made too inhomogeneously because also patients without nasal polyposis were included where IgE does not play a major role [178].

The effect of omalizumab is based on binding to the Cε3 region of the Fc fragment of the IgE molecule; the same structure also binds to the alpha chain of the highly affine receptor (FcεR1) on mast cells and basophils. The binding of omalizumab thus inhibits docking of IgE to the highly affine receptor, but binds in complexes that circulate in the blood for a long time and are finally degradated. Hence, omalizumab does not only bind free IgE in the serum but disarms mast cells and basophils in the tissue and blood that do no longer degranulate in cases of contact with the allergen or do no longer induce anaphylaxis [179]. As consequence, the expression of FcεR1 on these cells is reduced and the consecutive effects including eosinophilia are less important. At the same time the binding of IgE to the lowly affine receptor FcεRII is inhibited which reduces the IgE induced antigen presentation by dendritic cells. In this way the allergic reaction is again significantly attenuated.

Today, omalizumab is mainly applied as successful therapy in severe allergic asthma if asthma cannot be controlled by conventional asthma therapy and the patient is at risk because of exacerbations of his disease. Frequently, there is the additional requirement that a perennial allergen is proven, the meaningfulness of this claim must be questioned. The dosage of omalizumab should lead to a relevant reduction of the free IgE concentration in the blood, at the same time also IgE in the serum decreases. The dosage is calculated based on the total IgE in the blood (max. 1,500 kU/l) as well as the body weight of the patient. In cases of severe asthma, omalizumab leads to a significant reduction of the exacerbations of the disease and consecutively to a reduction of hospitalization (as well as the associated costs). Furthermore, it reduces the number and the impact of viral diseases especially in children [137]. Currently an even more effective anti-IgE molecule is being approved.

Despite the previous work on local production of IgE in nasal polyps and their functionality it was not clear if omalizumab reached the poorly vascularized tissue of nasal polyps in sufficient concentration and could develop its therapeutic effect in the sense of reduction of the nasal polyposis after binding of IgE. Additionally, about half of the patients are not atopic so that again the question of the importance of the IgE antibodies was asked. In those patients, asthma was often not allergic but classified as late-onset asthma. However, we had already explained previously that an increased IgE or SE-IgE in tissue of nasal polyps is found in 30–40% of the patients with CRSwNP, significantly increasing the risk of asthma [152]; furthermore we had also proven the functionality of local IgE antibodies [110]. The effectiveness of omalizumab would be another proof of the functionality of local IgE production in the upper and lower airways and would support the role of a non-atopic IgE synthesis induced by Staph. aureus.

The clinical effectiveness of omalizumab applied in the usual doses for severe asthma was examined in patients with severe polyposis and concomitant asthma (light to moderate) [180]. Omalizumab significantly reduced the score of nasal polyps (primary parameter) already after 8 weeks and after 16 weeks further reduction of the nasal polyps was found of a total of 2.6 score points; this corresponds to the effect of a therapy of 3 weeks with oral glucocorticosteroids (32 mg of methyl-prednisolone) and thus it is clinically relevant. Further, omalizumab significantly reduced the Lund-Mackay score, which measures the involvement of the paranasal sinuses in the disease, as well as the symptoms of the upper and lower airways including nasal obstruction, rhinorrhea, and smelling disorders, wheezing, and shortness of breath. Also quality of life parameters significantly improved with omalizumab in comparison to placebo, including the asthma quality of life (AQLQ). So it could be confirmed for the first time that the reduction of local IgE in selected CRSwNP patients was a worthwhile therapeutic objective.

Half of the patients treated with omalizumab were positive against inhalative allergens in the skin test and thus characterized as allergic. The others had no allergies. Although the number of patients in this study was limited and further studies will be necessary to clarify the effectiveness especially of non-allergic patients, a comparative analysis revealed a better response of non-allergic than allergic patients, especially in cases of asthma symptoms. Meanwhile, there are also reports on experiences with non-allergic asthma that confirm our results [181].

In this way, omalizumab demonstrated its clinical effectiveness in patients with nasal polyps and concomitant asthma over several weeks and it was well tolerated. Known risks such as anaphylactic reactions occurring in rare cases must be observed. Experiences in the clinic with patients who were treated primarily because of severe asthma and who had CRSwNP at the same time, confirmed the positive effects on the growth of the nasal polyps [182]. Nowadays we successfully apply omalizumab in patients with corticosteroid resistant recurrences of polyposis after at least one correctly performed surgery of the paranasal sinuses (in the sense of complete resection of the polyps) and concomitant (mostly not severe) asthma complaints. So this situation is outside asthma indication and we justify the application with the failure of conventional pharmacotherapy and surgery. Of course, the currently (still) high costs of the treatment have to be included in the indication (Figure 11 [Fig. 11]).

5.2 Anti-IL5 (Reslizumab, Mepolizumab)

About 80–85% of the nasal polyps in Europe, but only 10–50% of the polyps in Asia, have a Th2 inflammation pattern with prominent eosinophilia, expression of interleukin-5, and typical chemokines as well as activation markers for eosinophilic granulocytes. As IL-5 plays a key role in chemotaxis, differentiation, activation, and the survival of eosinophils and as those cells represent such a prominent characteristic in the polyps, the antagonism of IL-5 could offer a therapeutic chance. However, it was unclear if anti-IL-5 really reached the polyps and led to a reduction of eosinophils with diminution of the nasal polyps because polypous formations are also possible without eosinophilia and the association of eosinophils with edema is unclear.

In 1997, IL-5 was identified as key cytokine in nasal polyposis [100]; among a series of cytokines, IL-5 was most clearly associated with eosinophilia in nasal polyps and could be proven immunohistochemically also in eosinophils so that the cells themselves could be identified as source of the cytokine. In the same year we could also show in an ex-vitro model that anti-IL-5 antibodies, but not anti-IL-3 or anti-GM-CSF lead to cellular death (apoptosis) of the eosinophils [120]. Later, it could also be revealed that the regulation of IL-5 receptors plays a significant role in the localization of the cells in nasal polyps [183]. A first pilot study with reslizumab, a humanized anti-IL-5 antibody, showed a significant reduction of the size of the polyps in about 50% of the non-selected patients after only one intravenous injection. A high IL-5 level in nasal secretion seemed to predict the therapeutic response and also clearly decreased under verum therapy [184]. Hence, the principle of IL-5 antagonism was established in eosinophilic nasal polyps.

In a second study, this time with 2 IV injections of 750 mg of mepolizumab, of 30 patients with severe nasal polyposis (Davos 3-4 or recurrence after surgery) even with topical corticosteroids the results were mostly confirmed [101]. After 8 weeks, a significant reduction of the polyp score of at least one point was found in 60% of the patients treated with mepolizumab as well as a significant reduction of the CT score. Those patients who had a reduction of the polyp score of at least one point (“responders”) observed a remaining effect over nearly one year. So mepolizumab had a clinically relevant and in selected patients also long-lasting effect on nasal polyposis that did no longer respond to topical corticosteroids and thus would have had to undergo surgery. Like omalizumab, the quality of the effectiveness can certainly be considered as new dimension of therapeutic possibilities in nasal polyposis. Again, mepolizumab was well tolerated. Another long-term study with mepolizumab (principal investigator: Claus Bachert) has just been closed. The results are expected to be present in 2015. In the same year, also the approval of mepolizumab for asthma can be expected. However, currently it is still unclear if the drug will be approved for nasal polyps.

5.3 Anti-IL-4/-13 (Dupilumab)

As severe persisting respiratory diseases like CRSwNP and asthma must be classified as Th2 inflammations, innovative therapeutic approaches focus on Th2-associated cytokines. Beside interleukin-5, also IL-4 and IL-13 must be mentioned. Both cytokines act via two different receptors that partly overlap in their functions and they both contain the alpha sub-unit of the IL-4 receptor. The type 1 receptor that can only activated by IL-4 is mainly expressed on lymphocytes and regulates the differentiation of those cells. The type 2 receptor that is activated by IL-4 and IL-13 is expressed by a multitude of cells and has different functions, among them the production of the mucous secretion that is typical for nasal polyps. Dupilumab (SAR231893/REGN668) is a humanized antibody against the alpha sub-unit of the IL-4 receptor and can inhibit the effect of both cytokines, IL-4 and IL-13.

An investigation performed in the USA on severe asthma, the application of dupilumab could reduce the number of asthma exacerbations by 87% in comparison to placebo [185]. In this study, the patients were deprived of their asthma medication which led to a significant increase of exacerbations in the placebo group but not in the verum group. The pulmonary function in the verum group improved significantly. Furthermore it could be observed that different biomarkers of eosinophilic inflammation (FeNO, serum-IgE as well as the chemokines eotaxin-3 and TARC) were significantly reduced in the serum which confirms the biological activity of dupilumab. The clinical effect size of dupilumab seemed to be higher as the one of other biologics. As IL-4 and IL-13 also play a role in the pathogenesis of nasal polyps, we have performed a DBPCR study on the effectiveness and security of dupilumab in patients with CRSwNP with at least 5/8 score points in the polyp score with or without concomitant asthma. A total of 60 patients with bilateral nasal polyposis despite double dose of topical corticosteroids (mometasone furoate 2x daily) were observed for 4 weeks with topical corticosteroids and then they were treated either with 300 mg of subcutaneous dupilumab per week or placebo for additional 16 weeks. In the verum group the polyp score significantly decreased of 1.9 points compared to placebo (–0.3); also the CT score according to Lund and Mackay was significantly reduced (–8.8). The volume of the polyps in the maxillary sinuses was reduced by 32%, the SNOT-22 and the UPSIT smelling test revealed a significant effect compared to placebo. More than half of the patients responded with a reduction of the polyp score of at least 2 points (nearly similar to the effectiveness of 3 weeks of oral application of corticosteroids). The symptoms like nasal obstruction, rhinorrhea, and the subjective as well as objective smelling significantly improved in the verum group as also the nasal peak flow (PNIF, improvement of 60%).

Patients with asthma achieved a significantly improved pulmonary function (FEV1) and asthma control test (ALQ-5) in comparison to placebo. Patients with asthma also had a better reduction of the score of polyps compared to the total group (–2.4 score points in comparison to placebo). 56% of the patients had a reduction of the score of nasal polyps of more than 2 points.

Biomarkers of eonsinophilic inflammation were also significantly reduced, among them IgE, TARC, and eotaxin-3; in contrast to anti-IL-5, however, the absolute number of eosinophils in the blood died not decrease. The action profile of both biologics can be well differentiated while the clinical effectiveness of dupilumab seems to be superior to mepolizumab with comparable tolerability.

The results of this study are consistent with previous investigations of severe asthma and atopical dermatitis and they impressively confirm the potential of dupilumab to inhibit each type of Th2 induced inflammation and to reduce clinical complaints. For nasal polyps we could confirm this fact by subjective as well as objective parameters as additional effect being superior to basic therapy with topical corticosteroids. Also in this context the effect size is similar to the one of oral corticosteroids. Comparable to omalizumab, the patients with asthma also benefit from the significant improvement of their complaints regarding the lower airways.

5.4 Biomarkers

It is obvious that future ENT specialists will need other diagnostic tools beside endoscopes and CT scans allowing them to identify the endotype of each disease. Such surrogate markers could be determined most simply in the serum of the patients, as for example the absolute number of eosinophils in the blood, ECP as marker of activation of those cells, the total IgE as parameter of local IgE synthesis, IL-5Ra instead of IL-5 etc. Further possibilities are probably also chemokines such as TARC, PARC, eotaxin-3, or periostin. However, those markers are certainly increased in the tissue but – in contrast to asthma where the lung has a bigger production surface – the markers in the serum are often below the detection limit which seriously impairs the sensitivity of the test.

A primary objective would be to identify the Th2 type in the tissue. Probably even specific statements can be given on the involvement of single cytokines such as IL-4 vs. IL-5. The more successfully the individual endotype can be defined, the more precise is the statement about the prognosis (recurrence, asthma) and a personalized therapy can be started with prediction of the therapeutic effect of the according biologic. It must not be forgotten to mention that also other T helper cell reactions might be interesting for therapeutic interventions such as for example Th17, Tfh, Th22, and others. Currently large European cohort studies are performed on the question of serum markers.

5.5 Future approaches

There are a series of further therapeutic objectives as for example the antagonization of single cytokines of Th2 inflammation or their receptors like the IL-5 receptor alpha, TSLP. But also the deactivation of certain cells, especially of IgE producing B cells via a particular structure of the B cell binding molecule, M1 Prime, may even be a superordinate aim of research.

Although the development of those biologics is very promising, there are still some problems like for example the high costs of production and development of those substances, the necessity of systemic application, and the long-term effects that sometimes cannot be excluded. For instance, the question was discussed if omalizumab might increase the risk of malignant diseases. This suspicion could recently be disproved after many years of application [183].

It would be ideal to prefer local applications in the airways that minimizes the systemic risks, that achieves the therapeutic goal with small quantities, and that is consequently cheaper. As representatives of a series of such local approaches, two different approaches will be discussed here that have already been tested in humans and that provided the evidence of clinical effectiveness in mucosal surfaces.

5.5.1 Gene silencing, GATA3 DNA-zymes

The Th2 endotype is characterized by the predominance of activated Th2 cells that synthesize and release the cytokines IL-4, IL-5, and IL-13. The expression and production of those cytokines is controlled by the transcription factor GATA-3 that is relevant for the differentiation and activation of Th2 lymphocytes and is considered as “master switch” for all Th2 associated diseases. GATA-3 is overexpressed in nasal polyps, in asthma, and in atopic eczema. By reducing the released cytokines, a deactivation of the “master switch” would block also consecutive pathomechanisms such as for example the IgE production.

An innovative approach could thus deactivate all Th2 cytokines via a blockage of the transcription factor GATA-3 and also the associated phenomena of IgE production and tissue eosinophilia [186]. As GATA-3 is expressed intracellularly, so-called “antisense” or “silencing” techniques could be applied; molecules would have to be used the can penetrate the target cells (Th2). This approach was successful for GATA-3 via the development of a GATA-3 DNA-zyme in the sense that the DNA molecule docks to the GATA-3 RNA and quasi “cuts it up” by means of a catalytic enzyme. The DNA-zyme hdg40 is very stable and highly specific, at the same time, however, it is very active and easy to apply via inhalation or spray to the mucosa. In our laboratory we could show that GATA-3 DNA-zyme is absorbed without further transportation support in the T cells and significantly reduces the expression of GATA-3 RNA as well as IL-5 protein [187]. Applied in an asthma model in humans, hgd40 led to a significant reduction of the allergic immediate and late phases as well as the markers associated with a Th2 reaction. Thus it had a high potential in the treatment of Th2 associated diseases including CRSwNP and asthma, but also allergic rhinitis.

5.5.2 Genetically modified Lactococcus lactis (GM-LL)

Instead of complex antibodies that have to be produced and humanized in expensive processes in order to be applicable systemically, it is also possible today to choose approaches where proteins or their derivatives, for example nano-proteins, are produced direction on the mucosa by apathogenous bacteria. ActoGeniX, a spin-off of the University of Ghent, Belgium, has established the technology for development and production of genetically modified L. lacti and shown their pre-clinical and clinical applicability for a series of diseases, among them also allergic diseases. Some advantages are the local application, the possibility of producing every protein by GM-LL, and finally the possibility to have produced several therapeutically effective proteins by one single germ. This approach is currently investigated in pre-clinical studies.

5.5.3 Final remarks on biologics

It became obvious that the therapeutic approaches pursued up to now, as they are also summarized in the new EPOS guidelines, do not lead to long-term control of the symptoms or healing in all patients with their basic pillars of corticosteroids, antibiotics, and surgery. It is especially the group of Th2 associated diseases that is often accompanied by recurrences and comorbid asthma. The increased expression of the transcription factor GATA-3, the increased production of IL-4, IL-5 and IL-13 as well as an increased local production of IgE are characteristic for this immunologic situation and at the same time they indicate innovative objectives of intervention.

Biologics have a new opened dimension of effectiveness in comparison to oral corticosteroids; the response occurs more slowly but there effect is longer-lasting and they can be applied for several years without accumulation or side effects with comparable or even better response. Permanent application of oral corticosteroids would undoubtedly lead to health detriment that cannot be accepted. Currently, in particular the costs are an argument against the application of biologics.

It is certain that biologics currently will not replace the surgical possibilities where surgery leads to permanent success, for example in the therapy of CRSsNP. On the other hand, there are patients who suffer from severe Th2 inflammation with high probability of recurrence and the necessity of repeated interventions and with comorbid asthma where surgery cannot have a permanent effect and so in those cases an alternative therapy should be started. For those patients, biologics are a valuable alternative to repeated surgical revision. They are able to control the symptoms of the disease of the upper as well as the lower airways which according to our experience is often associated with a significantly increased quality of life.

We as ENT specialists, however, have to improve our knowledge of immunology in order to have sufficient knowhow in diagnostics and finally therapy with innovative drugs. We have to integrate the principle of endotyping at least in patients with severe respiratory diseases in our daily practice, refine the diagnostics by means of biomarkers, and understand the indications and side effects of biologics with the background of pathophysiology. Only then we will be in a position to offer our patients the possibilities of modern innovative treatment.


Notes

Conflict of interests

As principal investigator, Claus Bachert has contributed to studies with topical and oral corticosteroids, antibiotics, and biologics including omalizumab, reslizumab, mepolizumab, and dupilumab.

Funding

Claus Bachert’s projects have been supported by the Fund for Scientific Research Flanders (FWO-Vlaanderen: Mandat 1841713N and Projecte 3G.0489.08, Go39412N, G.0642.10N, G067512N), the University of Ghent BOF14/GOA/019 and 01J01113, the Interuniversity Attraction Poles Program (IUAP) – Belgian State – Belgian Science Policy P6/35 and P7/30, the European Commission’s 6th and 7th Framework programs FP-6/7 GALEN and PREDICTA.


References

1.
Fokkens WJ, Lund VJ, Mullol J, Bachert C, Alobid I, Baroody F, Cohen N, Cervin A, Douglas R, Gevaert P, Georgalas C, Goossens H, Harvey R, Hellings P, Hopkins C, Jones N, Joos G, Kalogjera L, Kern B, Kowalski M, Price D, Riechelmann H, Schlosser R, Senior B, Thomas M, Toskala E, Voegels R, Wang de Y, Wormald PJ. European Position Paper on Rhinosinusitis and Nasal Polyps 2012. Rhinol Suppl. 2012 Mar;(23):1-298.
2.
Bachert C, Van Bruaene N, Toskala E, Zhang N, Olze H, Scadding G, Van Drunen CM, Mullol J, Cardell L, Gevaert P, Van Zele T, Claeys S, Halldén C, Kostamo K, Foerster U, Kowalski M, Bieniek K, Olszewska-Ziaber A, Nizankowska-Mogilnicka E, Szczeklik A, Swierczynska M, Arcimowicz M, Lund V, Fokkens W, Zuberbier T, Akdis C, Canonica G, Van Cauwenberge P, Burney P, Bousquet J. Important research questions in allergy and related diseases: 3-chronic rhinosinusitis and nasal polyposis - a GALEN study. Allergy. 2009 Apr;64(4):520-33. DOI: 10.1111/j.1398-9995.2009.01964.x External link
3.
Tomassen P, Newson RB, Hoffmans R, Lötvall J, Cardell LO, Gunnbjörnsdóttir M, Thilsing T, Matricardi P, Krämer U, Makowska JS, Brozek G, Gjomarkaj M, Howarth P, Loureiro C, Toskala E, Fokkens W, Bachert C, Burney P, Jarvis D. Reliability of EP3OS symptom criteria and nasal endoscopy in the assessment of chronic rhinosinusitis--a GA² LEN study. Allergy. 2011 Apr;66(4):556-61. DOI: 10.1111/j.1398-9995.2010.02503.x External link
4.
Hastan D, Fokkens WJ, Bachert C, Newson RB, Bislimovska J, Bockelbrink A, Bousquet PJ, Brozek G, Bruno A, Dahlén SE, Forsberg B, Gunnbjörnsdóttir M, Kasper L, Krämer U, Kowalski ML, Lange B, Lundbäck B, Salagean E, Todo-Bom A, Tomassen P, Toskala E, van Drunen CM, Bousquet J, Zuberbier T, Jarvis D, Burney P. Chronic rhinosinusitis in Europe--an underestimated disease. A GA²LEN study. Allergy. 2011 Sep;66(9):1216-23. DOI: 10.1111/j.1398-9995.2011.02646.x External link
5.
Hamilos DL. Chronic rhinosinusitis: epidemiology and medical management. J Allergy Clin Immunol. 2011 Oct;128(4):693-707. DOI: 10.1016/j.jaci.2011.08.004 External link
6.
Jarvis D, Newson R, Lotvall J, Hastan D, Tomassen P, Keil T, Gjomarkaj M, Forsberg B, Gunnbjornsdottir M, Minov J, Brozek G, Dahlen SE, Toskala E, Kowalski ML, Olze H, Howarth P, Krämer U, Baelum J, Loureiro C, Kasper L, Bousquet PJ, Bousquet J, Bachert C, Fokkens W, Burney P. Asthma in adults and its association with chronic rhinosinusitis: the GA2LEN survey in Europe. Allergy. 2012 Jan;67(1):91-8. DOI: 10.1111/j.1398-9995.2011.02709.x External link
7.
Moore WC, Meyers DA, Wenzel SE, Teague WG, Li H, Li X, D'Agostino R Jr, Castro M, Curran-Everett D, Fitzpatrick AM, Gaston B, Jarjour NN, Sorkness R, Calhoun WJ, Chung KF, Comhair SA, Dweik RA, Israel E, Peters SP, Busse WW, Erzurum SC, Bleecker ER; National Heart, Lung, and Blood Institute's Severe Asthma Research Program. Identification of asthma phenotypes using cluster analysis in the Severe Asthma Research Program. Am J Respir Crit Care Med. 2010 Feb;181(4):315-23. DOI: 10.1164/rccm.200906-0896OC External link
8.
Dixon AE, Kaminsky DA, Holbrook JT, Wise RA, Shade DM, Irvin CG. Allergic rhinitis and sinusitis in asthma: differential effects on symptoms and pulmonary function. Chest. 2006 Aug;130(2):429-35. DOI: 10.1378/chest.130.2.429 External link
9.
Van Zele T, Holtappels G, Gevaert P, Bachert C. Differences in initial immunoprofiles between recurrent and nonrecurrent chronic rhinosinusitis with nasal polyps. Am J Rhinol Allergy. 2014 May-Jun;28(3):192-8. DOI: 10.2500/ajra.2014.28.4033 External link
10.
Bossé Y, Bacot F, Montpetit A, Rung J, Qu HQ, Engert JC, Polychronakos C, Hudson TJ, Froguel P, Sladek R, Desrosiers M. Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans. Hum Genet. 2009 Apr;125(3):305-18. DOI: 10.1007/s00439-009-0626-9 External link
11.
Hsu J, Avila PC, Kern RC, Hayes MG, Schleimer RP, Pinto JM. Genetics of chronic rhinosinusitis: state of the field and directions forward. J Allergy Clin Immunol. 2013 Apr;131(4):977-93, DOI: 10.1016/j.jaci.2013.01.028 External link
12.
Henmyr V, Vandeplas G, Halldén C, Säll T, Olze H, Bachert C, Cardell LO. Replication study of genetic variants associated with chronic rhinosinusitis and nasal polyposis. J Allergy Clin Immunol. 2014 Jan;133(1):273-5. DOI: 10.1016/j.jaci.2013.08.011 External link
13.
Kim SH, Park HS, Holloway JW, Shin HD, Park CS. Association between a TGFbeta1 promoter polymorphism and rhinosinusitis in aspirin-intolerant asthmatic patients. Respir Med. 2007 Mar;101(3):490-5. DOI: 10.1016/j.rmed.2006.07.002 External link
14.
Zhang Y, Endam LM, Filali-Mouhim A, Bossé Y, Castano R, Desrosiers M. Polymorphisms in the nitric oxide synthase 1 gene are associated with severe chronic rhinosinusitis. Am J Rhinol Allergy. 2011 Mar-Apr;25(2):e49-54. DOI: 10.2500/ajra.2011.25.3588 External link
15.
Zuo L, Koozechian MS, Chen LL. Characterization of reactive nitrogen species in allergic asthma. Ann Allergy Asthma Immunol. 2014 Jan;112(1):18-22. DOI: 10.1016/j.anai.2013.10.007 External link
16.
Lee RJ, Chen B, Redding KM, Margolskee RF, Cohen NA. Mouse nasal epithelial innate immune responses to Pseudomonas aeruginosa quorum-sensing molecules require taste signaling components. Innate Immun. 2013 Sep;20(6):606-17. DOI: 10.1177/1753425913503386 External link
17.
Zhang Y, Endam LM, Filali-Mouhim A, Zhao L, Desrosiers M, Han D, Zhang L. Polymorphisms in RYBP and AOAH genes are associated with chronic rhinosinusitis in a Chinese population: a replication study. PLoS ONE. 2012;7(6):e39247. DOI: 10.1371/journal.pone.0039247 External link
18.
Barnes KC, Grant A, Gao P, Baltadjieva D, Berg T, Chi P, Zhang S, Zambelli-Weiner A, Ehrlich E, Zardkoohi O, Brummet ME, Stockton M, Watkins T, Gao L, Gittens M, Wills-Karp M, Cheadle C, Beck LA, Beaty TH, Becker KG, Garcia JG, Mathias RA. Polymorphisms in the novel gene acyloxyacyl hydroxylase (AOAH) are associated with asthma and associated phenotypes. J Allergy Clin Immunol. 2006 Jul;118(1):70-7. DOI: 10.1016/j.jaci.2006.03.036 External link
19.
Cheong HS, Park SM, Kim MO, Park JS, Lee JY, Byun JY, Park BL, Shin HD, Park CS. Genome-wide methylation profile of nasal polyps: relation to aspirin hypersensitivity in asthmatics. Allergy. 2011 May;66(5):637-44. DOI: 10.1111/j.1398-9995.2010.02514.x External link
20.
Seiberling KA, Church CA, Herring JL, Sowers LC. Epigenetics of chronic rhinosinusitis and the role of the eosinophil. Int Forum Allergy Rhinol. 2012 Jan-Feb;2(1):80-4. DOI: 10.1002/alr.20090 External link
21.
Van Bruaene N, Derycke L, Perez-Novo CA, Gevaert P, Holtappels G, De Ruyck N, Cuvelier C, Van Cauwenberge P, Bachert C. TGF-beta signaling and collagen deposition in chronic rhinosinusitis. J Allergy Clin Immunol. 2009 Aug;124(2):253-9. DOI: 10.1016/j.jaci.2009.04.013 External link
22.
Cho JS, Moon YM, Park IH, Um JY, Moon JH, Park SJ, Lee SH, Kang HJ, Lee HM. Epigenetic regulation of myofibroblast differentiation and extracellular matrix production in nasal polyp-derived fibroblasts. Clin Exp Allergy. 2012 Jun;42(6):872-82. DOI: 10.1111/j.1365-2222.2011.03931.x External link
23.
Zhang XH, Zhang YN, Li HB, Hu CY, Wang N, Cao PP, Liao B, Lu X, Cui YH, Liu Z. Overexpression of miR-125b, a novel regulator of innate immunity, in eosinophilic chronic rhinosinusitis with nasal polyps. Am J Respir Crit Care Med. 2012 Jan;185(2):140-51. DOI: 10.1164/rccm.201103-0456OC External link
24.
Johansson ME, Larsson JM, Hansson GC. The two mucus layers of colon are organized by the MUC2 mucin, whereas the outer layer is a legislator of host-microbial interactions. Proc Natl Acad Sci USA. 2011 Mar;108 Suppl 1:4659-65. DOI: 10.1073/pnas.1006451107 External link
25.
Zhang Y, Wang X, Wang H, Jiao J, Li Y, Fan E, Zhang L, Bachert C. TMEM16A-Mediated Mucin Secretion in IL-13-Induced Nasal Epithelial Cells From Chronic Rhinosinusitis Patients. Allergy Asthma Immunol Res. 2015 Jul;7(4):367-75. DOI: 10.4168/aair.2015.7.4.367 External link
26.
Avila P, Schleimer RP. Airway Epithelium. In: Kay AB, Kaplan AP, Bousquet J, Holt PG, editors. Allergy and allergic diseases. 2nd ed. Oxford: Wiley-Blackwell; 2008. DOI: 10.1002/9781444300918.ch16 External link
27.
Laudien M, Dressel S, Harder J, Gläser R. Differential expression pattern of antimicrobial peptides in nasal mucosa and secretion. Rhinology. 2011 Mar;49(1):107-11. DOI: 10.4193/Rhino10.036 External link
28.
Meyer JE, Harder J, Sipos B, Maune S, Klöppel G, Bartels J, Schröder JM, Gläser R. Psoriasin (S100A7) is a principal antimicrobial peptide of the human tongue. Mucosal Immunol. 2008 May;1(3):239-43. DOI: 10.1038/mi.2008.3 External link
29.
Ramanathan M Jr, Lee WK, Spannhake EW, Lane AP. Th2 cytokines associated with chronic rhinosinusitis with polyps down-regulate the antimicrobial immune function of human sinonasal epithelial cells. Am J Rhinol. 2008 Mar-Apr;22(2):115-21. DOI: 10.2500/ajr.2008.22.3136 External link
30.
Aujla SJ, Chan YR, Zheng M, Fei M, Askew DJ, Pociask DA, Reinhart TA, McAllister F, Edeal J, Gaus K, Husain S, Kreindler JL, Dubin PJ, Pilewski JM, Myerburg MM, Mason CA, Iwakura Y, Kolls JK. IL-22 mediates mucosal host defense against Gram-negative bacterial pneumonia. Nat Med. 2008 Mar;14(3):275-81. DOI: 10.1038/nm1710 External link
31.
Pickert G, Neufert C, Leppkes M, Zheng Y, Wittkopf N, Warntjen M, Lehr HA, Hirth S, Weigmann B, Wirtz S, Ouyang W, Neurath MF, Becker C. STAT3 links IL-22 signaling in intestinal epithelial cells to mucosal wound healing. J Exp Med. 2009 Jul;206(7):1465-72. DOI: 10.1084/jem.20082683 External link
32.
Ramanathan M Jr, Spannhake EW, Lane AP. Chronic rhinosinusitis with nasal polyps is associated with decreased expression of mucosal interleukin 22 receptor. Laryngoscope. 2007 Oct;117(10):1839-43. DOI: 10.1097/MLG.0b013e31811edd4f External link
33.
Peters M, Dudziak K, Stiehm M, Bufe A. T-cell polarization depends on concentration of the danger signal used to activate dendritic cells. Immunol Cell Biol. 2010 Jul;88(5):537-44. DOI: 10.1038/icb.2010.3 External link
34.
Lee RJ, Kofonow JM, Rosen PL, Siebert AP, Chen B, Doghramji L, Xiong G, Adappa ND, Palmer JN, Kennedy DW, Kreindler JL, Margolskee RF, Cohen NA. Bitter and sweet taste receptors regulate human upper respiratory innate immunity. J Clin Invest. 2014 Mar;124(3):1393-405. DOI: 10.1172/JCI72094 External link
35.
Rogers GA, Den Beste K, Parkos CA, Nusrat A, Delgaudio JM, Wise SK. Epithelial tight junction alterations in nasal polyposis. Int Forum Allergy Rhinol. 2011 Jan-Feb;1(1):50-4. DOI: 10.1002/alr.20014 External link
36.
Zuckerman JD, Lee WY, DelGaudio JM, Moore CE, Nava P, Nusrat A, Parkos CA. Pathophysiology of nasal polyposis: the role of desmosomal junctions. Am J Rhinol. 2008 Nov-Dec;22(6):589-97. DOI: 10.2500/ajr.2008.22.3235 External link
37.
Tieu DD, Peters AT, Carter RG, Carter RT, Suh L, Conley DB, Chandra R, Norton J, Grammer LC, Harris KE, Kato A, Kern RC, Schleimer RP. Evidence for diminished levels of epithelial psoriasin and calprotectin in chronic rhinosinusitis. J Allergy Clin Immunol. 2010 Mar;125(3):667-75. DOI: 10.1016/j.jaci.2009.11.045 External link
38.
Soyka MB, Wawrzyniak P, Eiwegger T, Holzmann D, Treis A, Wanke K, Kast JI, Akdis CA. Defective epithelial barrier in chronic rhinosinusitis: the regulation of tight junctions by IFN-γ and IL-4. J Allergy Clin Immunol. 2012 Nov;130(5):1087-96. DOI: 10.1016/j.jaci.2012.05.052 External link
39.
Meng J, Zhou P, Liu Y, Liu F, Yi X, Liu S, Holtappels G, Bachert C, Zhang N. The development of nasal polyp disease involves early nasal mucosal inflammation and remodelling. PLoS ONE. 2013;8(12):e82373. DOI: 10.1371/journal.pone.0082373 External link
40.
Schleimer RP, Kato A, Kern R, Kuperman D, Avila PC. Epithelium: at the interface of innate and adaptive immune responses. J Allergy Clin Immunol. 2007 Dec;120(6):1279-84. DOI: 10.1016/j.jaci.2007.08.046 External link
41.
Claeys S, de Belder T, Holtappels G, Gevaert P, Verhasselt B, van Cauwenberge P, Bachert C. Human beta-defensins and toll-like receptors in the upper airway. Allergy. 2003 Aug;58(8):748-53. DOI: 10.1034/j.1398-9995.2003.00180.x External link
42.
Vandermeer J, Sha Q, Lane AP, Schleimer RP. Innate immunity of the sinonasal cavity: expression of messenger RNA for complement cascade components and toll-like receptors. Arch Otolaryngol Head Neck Surg. 2004 Dec;130(12):1374-80. DOI: 10.1001/archotol.130.12.1374 External link
43.
Kawai T, Akira S. Toll-like receptors and their crosstalk with other innate receptors in infection and immunity. Immunity. 2011 May;34(5):637-50. DOI: 10.1016/j.immuni.2011.05.006 External link
44.
Lane AP, Truong-Tran QA, Myers A, Bickel C, Schleimer RP. Serum amyloid A, properdin, complement 3, and toll-like receptors are expressed locally in human sinonasal tissue. Am J Rhinol. 2006 Jan-Feb;20(1):117-23.
45.
Zhao CY, Wang X, Liu M, Jin DJ. Microarray gene analysis of Toll-like receptor signaling elements in chronic rhinosinusitis with nasal polyps. Int Arch Allergy Immunol. 2011;156(3):297-304. DOI: 10.1159/000323767 External link
46.
Sun Y, Zhou B, Wang C, Huang Q, Zhang Q, Han Y, Dai W, Fan E, Li Y. Biofilm formation and Toll-like receptor 2, Toll-like receptor 4, and NF-kappaB expression in sinus tissues of patients with chronic rhinosinusitis. Am J Rhinol Allergy. 2012 Mar-Apr;26(2):104-9. DOI: 10.2500/ajra.2012.26.3718 External link
47.
Kato A, Schleimer RP. Beyond inflammation: airway epithelial cells are at the interface of innate and adaptive immunity. Curr Opin Immunol. 2007 Dec;19(6):711-20. DOI: 10.1016/j.coi.2007.08.004 External link
48.
Bogefors J, Rydberg C, Uddman R, Fransson M, Månsson A, Benson M, Adner M, Cardell LO. Nod1, Nod2 and Nalp3 receptors, new potential targets in treatment of allergic rhinitis? Allergy. 2010 Oct;65(10):1222-6. DOI: 10.1111/j.1398-9995.2009.02315.x External link
49.
Rudack C, Steinhoff M, Mooren F, Buddenkotte J, Becker K, von Eiff C, Sachse F. PAR-2 activation regulates IL-8 and GRO-alpha synthesis by NF-kappaB, but not RANTES, IL-6, eotaxin or TARC expression in nasal epithelium. Clin Exp Allergy. 2007 Jul;37(7):1009-22. DOI: 10.1111/j.1365-2222.2007.02686.x External link
50.
Ossovskaya VS, Bunnett NW. Protease-activated receptors: contribution to physiology and disease. Physiol Rev. 2004 Apr;84(2):579-621. DOI: 10.1152/physrev.00028.2003 External link
51.
Vroling AB, Fokkens WJ, van Drunen CM. How epithelial cells detect danger: aiding the immune response. Allergy. 2008 Sep;63(9):1110-23. DOI: 10.1111/j.1398-9995.2008.01785.x External link
52.
Rudack C, Sachse F, Albert N, Becker K, von Eiff C. Immunomodulation of nasal epithelial cells by Staphylococcus aureus-derived serine proteases. J Immunol. 2009 Dec;183(11):7592-601. DOI: 10.4049/jimmunol.0803902 External link
53.
Iwasaki A, Medzhitov R. Toll-like receptor control of the adaptive immune responses. Nat Immunol. 2004 Oct;5(10):987-95. DOI: 10.1038/ni1112 External link
54.
Oppenheim JJ, Yang D. Alarmins: chemotactic activators of immune responses. Curr Opin Immunol. 2005 Aug;17(4):359-65. DOI: 10.1016/j.coi.2005.06.002 External link
55.
Bianchi ME. DAMPs, PAMPs and alarmins: all we need to know about danger. J Leukoc Biol. 2007 Jan;81(1):1-5. DOI: 10.1189/jlb.0306164 External link
56.
Lotze MT, Zeh HJ, Rubartelli A, Sparvero LJ, Amoscato AA, Washburn NR, Devera ME, Liang X, Tör M, Billiar T. The grateful dead: damage-associated molecular pattern molecules and reduction/oxidation regulate immunity. Immunol Rev. 2007 Dec;220:60-81. DOI: 10.1111/j.1600-065X.2007.00579.x External link
57.
Piccinini AM, Midwood KS. DAMPening inflammation by modulating TLR signalling. Mediators Inflamm. 2010;2010:672395. DOI: 10.1155/2010/672395 External link
58.
Van Crombruggen K, Holtappels G, De Ruyck N, Derycke L, Tomassen P, Bachert C. RAGE processing in chronic airway conditions: involvement of Staphylococcus aureus and ECP. J Allergy Clin Immunol. 2012 Jun;129(6):1515-21.e8. DOI: 10.1016/j.jaci.2012.02.021 External link
59.
Rubartelli A, Lotze MT. Inside, outside, upside down: damage-associated molecular-pattern molecules (DAMPs) and redox. Trends Immunol. 2007 Oct;28(10):429-36. DOI: 10.1016/j.it.2007.08.004 External link
60.
Hudson BI, Carter AM, Harja E, Kalea AZ, Arriero M, Yang H, Grant PJ, Schmidt AM. Identification, classification, and expression of RAGE gene splice variants. FASEB J. 2008 May;22(5):1572-80. DOI: 10.1096/fj.07-9909com External link
61.
Yamakawa N, Uchida T, Matthay MA, Makita K. Proteolytic release of the receptor for advanced glycation end products from in vitro and in situ alveolar epithelial cells. Am J Physiol Lung Cell Mol Physiol. 2011 Apr;300(4):L516-25. DOI: 10.1152/ajplung.00118.2010 External link
62.
Bopp C, Bierhaus A, Hofer S, Bouchon A, Nawroth PP, Martin E, Weigand MA. Bench-to-bedside review: The inflammation-perpetuating pattern-recognition receptor RAGE as a therapeutic target in sepsis. Crit Care. 2008;12(1):201. DOI: 10.1186/cc6164 External link
63.
Bierhaus A, Humpert PM, Morcos M, Wendt T, Chavakis T, Arnold B, Stern DM, Nawroth PP. Understanding RAGE, the receptor for advanced glycation end products. J Mol Med. 2005 Nov;83(11):876-86. DOI: 10.1007/s00109-005-0688-7 External link
64.
Pullerits R, Brisslert M, Jonsson IM, Tarkowski A. Soluble receptor for advanced glycation end products triggers a proinflammatory cytokine cascade via beta2 integrin Mac-1. Arthritis Rheum. 2006 Dec;54(12):3898-907. DOI: 10.1002/art.22217 External link
65.
Englert JM, Hanford LE, Kaminski N, Tobolewski JM, Tan RJ, Fattman CL, Ramsgaard L, Richards TJ, Loutaev I, Nawroth PP, Kasper M, Bierhaus A, Oury TD. A role for the receptor for advanced glycation end products in idiopathic pulmonary fibrosis. Am J Pathol. 2008 Mar;172(3):583-91. DOI: 10.2353/ajpath.2008.070569 External link
66.
Demling N, Ehrhardt C, Kasper M, Laue M, Knels L, Rieber EP. Promotion of cell adherence and spreading: a novel function of RAGE, the highly selective differentiation marker of human alveolar epithelial type I cells. Cell Tissue Res. 2006 Mar;323(3):475-88. DOI: 10.1007/s00441-005-0069-0 External link
67.
Li X, Meng J, Qiao X, Liu Y, Liu F, Zhang N, Zhang J, Holtappels G, Luo B, Zhou P, Zheng Y, Lin P, Liu S, Bachert C. Expression of TGF, matrix metalloproteinases, and tissue inhibitors in Chinese chronic rhinosinusitis. J Allergy Clin Immunol. 2010 May;125(5):1061-8. DOI: 10.1016/j.jaci.2010.02.023 External link
68.
Queisser MA, Kouri FM, Königshoff M, Wygrecka M, Schubert U, Eickelberg O, Preissner KT. Loss of RAGE in pulmonary fibrosis: molecular relations to functional changes in pulmonary cell types. Am J Respir Cell Mol Biol. 2008 Sep;39(3):337-45. DOI: 10.1165/rcmb.2007-0244OC External link
69.
Van Zele T, Gevaert P, Watelet JB, Claeys G, Holtappels G, Claeys C, van Cauwenberge P, Bachert C. Staphylococcus aureus colonization and IgE antibody formation to enterotoxins is increased in nasal polyposis. J Allergy Clin Immunol. 2004 Oct;114(4):981-3. DOI: 10.1016/j.jaci.2004.07.013 External link
70.
Chen Y, Akirav EM, Chen W, Henegariu O, Moser B, Desai D, Shen JM, Webster JC, Andrews RC, Mjalli AM, Rothlein R, Schmidt AM, Clynes R, Herold KC. RAGE ligation affects T cell activation and controls T cell differentiation. J Immunol. 2008 Sep;181(6):4272-8. DOI: 10.4049/jimmunol.181.6.4272 External link
71.
Vogl T, Tenbrock K, Ludwig S, Leukert N, Ehrhardt C, van Zoelen MA, Nacken W, Foell D, van der Poll T, Sorg C, Roth J. Mrp8 and Mrp14 are endogenous activators of Toll-like receptor 4, promoting lethal, endotoxin-induced shock. Nat Med. 2007 Sep;13(9):1042-9. DOI: 10.1038/nm1638 External link
72.
Loser K, Vogl T, Voskort M, Lueken A, Kupas V, Nacken W, Klenner L, Kuhn A, Foell D, Sorokin L, Luger TA, Roth J, Beissert S. The Toll-like receptor 4 ligands Mrp8 and Mrp14 are crucial in the development of autoreactive CD8+ T cells. Nat Med. 2010 Jun;16(6):713-7. DOI: 10.1038/nm.2150 External link
73.
Sparvero LJ, Asafu-Adjei D, Kang R, Tang D, Amin N, Im J, Rutledge R, Lin B, Amoscato AA, Zeh HJ, Lotze MT. RAGE (Receptor for Advanced Glycation Endproducts), RAGE ligands, and their role in cancer and inflammation. J Transl Med. 2009;7:17. DOI: 10.1186/1479-5876-7-17 External link
74.
Richer SL, Truong-Tran AQ, Conley DB, Carter R, Vermylen D, Grammer LC, Peters AT, Chandra RK, Harris KE, Kern RC, Schleimer RP. Epithelial genes in chronic rhinosinusitis with and without nasal polyps. Am J Rhinol. 2008 May-Jun;22(3):228-34. DOI: 10.2500/ajr.2008.22.3162 External link
75.
White ES, Baralle FE, Muro AF. New insights into form and function of fibronectin splice variants. J Pathol. 2008 Sep;216(1):1-14. DOI: 10.1002/path.2388 External link
76.
Van Crombruggen K, Zhang N, Gevaert P, Tomassen P, Bachert C. Pathogenesis of chronic rhinosinusitis: inflammation. J Allergy Clin Immunol. 2011 Oct;128(4):728-32. DOI: 10.1016/j.jaci.2011.07.049 External link
77.
Okamura Y, Watari M, Jerud ES, Young DW, Ishizaka ST, Rose J, Chow JC, Strauss JF 3rd. The extra domain A of fibronectin activates Toll-like receptor 4. J Biol Chem. 2001 Mar;276(13):10229-33. DOI: 10.1074/jbc.M100099200 External link
78.
Menzies BE. The role of fibronectin binding proteins in the pathogenesis of Staphylococcus aureus infections. Curr Opin Infect Dis. 2003 Jun;16(3):225-9. DOI: 10.1097/01.qco.0000073771.11390.75 External link
79.
Henderson B, Nair S, Pallas J, Williams MA. Fibronectin: a multidomain host adhesin targeted by bacterial fibronectin-binding proteins. FEMS Microbiol Rev. 2011 Jan;35(1):147-200. DOI: 10.1111/j.1574-6976.2010.00243.x External link
80.
Hammad H, Lambrecht BN. Dendritic cells and airway epithelial cells at the interface between innate and adaptive immune responses. Allergy. 2011 May;66(5):579-87. DOI: 10.1111/j.1398-9995.2010.02528.x External link
81.
Hazenberg MD, Spits H. Human innate lymphoid cells. Blood. 2014 Jul;124(5):700-9. DOI: 10.1182/blood-2013-11-427781 External link
82.
Mjösberg JM, Trifari S, Crellin NK, Peters CP, van Drunen CM, Piet B, Fokkens WJ, Cupedo T, Spits H. Human IL-25- and IL-33-responsive type 2 innate lymphoid cells are defined by expression of CRTH2 and CD161. Nat Immunol. 2011 Nov;12(11):1055-62. DOI: 10.1038/ni.2104 External link
83.
Shikotra A, Choy DF, Ohri CM, Doran E, Butler C, Hargadon B, Shelley M, Abbas AR, Austin CD, Jackman J, Wu LC, Heaney LG, Arron JR, Bradding P. Increased expression of immunoreactive thymic stromal lymphopoietin in patients with severe asthma. J Allergy Clin Immunol. 2012 Jan;129(1):104-11.e1-9. DOI: 10.1016/j.jaci.2011.08.031 External link
84.
Barnig C, Cernadas M, Dutile S, Liu X, Perrella MA, Kazani S, Wechsler ME, Israel E, Levy BD. Lipoxin A4 regulates natural killer cell and type 2 innate lymphoid cell activation in asthma. Sci Transl Med. 2013 Feb;5(174):174ra26. DOI: 10.1126/scitranslmed.3004812 External link
85.
Pérez-Novo CA, Watelet JB, Claeys C, Van Cauwenberge P, Bachert C. Prostaglandin, leukotriene, and lipoxin balance in chronic rhinosinusitis with and without nasal polyposis. J Allergy Clin Immunol. 2005 Jun;115(6):1189-96. DOI: 10.1016/j.jaci.2005.02.029 External link
86.
Pérez-Novo CA, Holtappels G, Vinall SL, Xue L, Zhang N, Bachert C, Pettipher R. CRTH2 mediates the activation of human Th2 cells in response to PGD(2) released from IgE/anti-IgE treated nasal polyp tissue. Allergy. 2010 Mar;65(3):304-10. DOI: 10.1111/j.1398-9995.2009.02204.x External link
87.
Demedts IK, Bracke KR, Maes T, Joos GF, Brusselle GG. Different roles for human lung dendritic cell subsets in pulmonary immune defense mechanisms. Am J Respir Cell Mol Biol. 2006 Sep;35(3):387-93. DOI: 10.1165/rcmb.2005-0382OC External link
88.
Reinartz SM, van Tongeren J, van Egmond D, de Groot EJ, Fokkens WJ, van Drunen CM. Dendritic cells in nasal mucosa of subjects with different allergic sensitizations. J Allergy Clin Immunol. 2011 Oct;128(4):887-90. DOI: 10.1016/j.jaci.2011.06.001 External link
89.
Pezato R, Pérez-Novo CA, Holtappels G, De Ruyck N, Van Crombruggen K, De Vos G, Bachert C, Derycke L. The expression of dendritic cell subsets in severe chronic rhinosinusitis with nasal polyps is altered. Immunobiology. 2014 Sep;219(9):729-36. DOI: 10.1016/j.imbio.2014.05.004 External link
90.
Martinez FO, Helming L, Gordon S. Alternative activation of macrophages: an immunologic functional perspective. Annu Rev Immunol. 2009;27:451-83. DOI: 10.1146/annurev.immunol.021908.132532 External link
91.
Sica A, Mantovani A. Macrophage plasticity and polarization: in vivo veritas. J Clin Invest. 2012 Mar;122(3):787-95. DOI: 10.1172/JCI59643 External link
92.
Gordon S. Alternative activation of macrophages. Nat Rev Immunol. 2003 Jan;3(1):23-35. DOI: 10.1038/nri978 External link
93.
Krysko O, Holtappels G, Zhang N, Kubica M, Deswarte K, Derycke L, Claeys S, Hammad H, Brusselle GG, Vandenabeele P, Krysko DV, Bachert C. Alternatively activated macrophages and impaired phagocytosis of S. aureus in chronic rhinosinusitis. Allergy. 2011 Mar;66(3):396-403. DOI: 10.1111/j.1398-9995.2010.02498.x External link
94.
Peterson S, Poposki JA, Nagarkar DR, Chustz RT, Peters AT, Suh LA, Carter R, Norton J, Harris KE, Grammer LC, Tan BK, Chandra RK, Conley DB, Kern RC, Schleimer RP, Kato A. Increased expression of CC chemokine ligand 18 in patients with chronic rhinosinusitis with nasal polyps. J Allergy Clin Immunol. 2012 Jan;129(1):119-27.e1-9. DOI: 10.1016/j.jaci.2011.08.021 External link
95.
Van Zele T, Claeys S, Gevaert P, Van Maele G, Holtappels G, Van Cauwenberge P, Bachert C. Differentiation of chronic sinus diseases by measurement of inflammatory mediators. Allergy. 2006 Nov;61(11):1280-9. DOI: 10.1111/j.1398-9995.2006.01225.x External link
96.
Lan F, Zhang N, Zhang J, Krysko O, Zhang Q, Xian J, Derycke L, Qi Y, Li K, Liu S, Lin P, Bachert C. Forkhead box protein 3 in human nasal polyp regulatory T cells is regulated by the protein suppressor of cytokine signaling 3. J Allergy Clin Immunol. 2013 Dec;132(6):1314-21. DOI: 10.1016/j.jaci.2013.06.010 External link
97.
Zhang N, Van Zele T, Perez-Novo C, Van Bruaene N, Holtappels G, DeRuyck N, Van Cauwenberge P, Bachert C. Different types of T-effector cells orchestrate mucosal inflammation in chronic sinus disease. J Allergy Clin Immunol. 2008 Nov;122(5):961-8. DOI: 10.1016/j.jaci.2008.07.008 External link
98.
Derycke L, Eyerich S, Van Crombruggen K, Pérez-Novo C, Holtappels G, Deruyck N, Gevaert P, Bachert C. Mixed T helper cell signatures in chronic rhinosinusitis with and without polyps. PLoS ONE. 2014;9(6):e97581. DOI: 10.1371/journal.pone.0097581 External link
99.
Bachert C, Zhang N, Holtappels G, De Lobel L, van Cauwenberge P, Liu S, Lin P, Bousquet J, Van Steen K. Presence of IL-5 protein and IgE antibodies to staphylococcal enterotoxins in nasal polyps is associated with comorbid asthma. J Allergy Clin Immunol. 2010 Nov;126(5):962-8. DOI: 10.1016/j.jaci.2010.07.007 External link
100.
Bachert C, Wagenmann M, Hauser U, Rudack C. IL-5 synthesis is upregulated in human nasal polyp tissue. J Allergy Clin Immunol. 1997 Jun;99(6 Pt 1):837-42. DOI: 10.1016/S0091-6749(97)80019-X External link
101.
Gevaert P, Van Bruaene N, Cattaert T, Van Steen K, Van Zele T, Acke F, De Ruyck N, Blomme K, Sousa AR, Marshall RP, Bachert C. Mepolizumab, a humanized anti-IL-5 mAb, as a treatment option for severe nasal polyposis. J Allergy Clin Immunol. 2011 Nov;128(5):989-95.e1-8. DOI: 10.1016/j.jaci.2011.07.056 External link
102.
Van Zele T, Gevaert P, Holtappels G, van Cauwenberge P, Bachert C. Local immunoglobulin production in nasal polyposis is modulated by superantigens. Clin Exp Allergy. 2007 Dec;37(12):1840-7. DOI: 10.1111/j.1365-2222.2007.02838.x External link
103.
Gevaert P, Nouri-Aria KT, Wu H, Harper CE, Takhar P, Fear DJ, Acke F, De Ruyck N, Banfield G, Kariyawasam HH, Bachert C, Durham SR, Gould HJ. Local receptor revision and class switching to IgE in chronic rhinosinusitis with nasal polyps. Allergy. 2013 Jan;68(1):55-63. DOI: 10.1111/all.12054 External link
104.
Mechtcheriakova D, Sobanov Y, Holtappels G, Bajna E, Svoboda M, Jaritz M, Bachert C, Jensen-Jarolim E. Activation-induced cytidine deaminase (AID)-associated multigene signature to assess impact of AID in etiology of diseases with inflammatory component. PLoS ONE. 2011;6(10):e25611. DOI: 10.1371/journal.pone.0025611 External link
105.
Kato A, Peters A, Suh L, Carter R, Harris KE, Chandra R, Conley D, Grammer LC, Kern R, Schleimer RP. Evidence of a role for B cell-activating factor of the TNF family in the pathogenesis of chronic rhinosinusitis with nasal polyps. J Allergy Clin Immunol. 2008 Jun;121(6):1385-92. DOI: 10.1016/j.jaci.2008.03.002 External link
106.
Mackay F, Schneider P. Cracking the BAFF code. Nat Rev Immunol. 2009 Jul;9(7):491-502. DOI: 10.1038/nri2572 External link
107.
Kallies A, Nutt SL. Terminal differentiation of lymphocytes depends on Blimp-1. Curr Opin Immunol. 2007 Apr;19(2):156-62. DOI: 10.1016/j.coi.2007.01.003 External link
108.
Coker HA, Durham SR, Gould HJ. Local somatic hypermutation and class switch recombination in the nasal mucosa of allergic rhinitis patients. J Immunol. 2003 Nov;171(10):5602-10. DOI: 10.4049/jimmunol.171.10.5602 External link
109.
Tan BK, Li QZ, Suh L, Kato A, Conley DB, Chandra RK, Zhou J, Norton J, Carter R, Hinchcliff M, Harris K, Peters A, Grammer LC, Kern RC, Mohan C, Schleimer RP. Evidence for intranasal antinuclear autoantibodies in patients with chronic rhinosinusitis with nasal polyps. J Allergy Clin Immunol. 2011 Dec;128(6):1198-1206.e1. DOI: 10.1016/j.jaci.2011.08.037 External link
110.
Zhang N, Holtappels G, Gevaert P, Patou J, Dhaliwal B, Gould H, Bachert C. Mucosal tissue polyclonal IgE is functional in response to allergen and SEB. Allergy. 2011 Jan;66(1):141-8. DOI: 10.1111/j.1398-9995.2010.02448.x External link
111.
Kowalski ML, Lewandowska-Polak A, Woźniak J, Ptasińska A, Jankowski A, Wagrowska-Danilewicz M, Danilewicz M, Pawliczak R. Association of stem cell factor expression in nasal polyp epithelial cells with aspirin sensitivity and asthma. Allergy. 2005 May;60(5):631-7. DOI: 10.1111/j.1398-9995.2005.00753.x External link
112.
Pawankar R, Lee KH, Nonaka M, Takizawa R. Role of mast cells and basophils in chronic rhinosinusitis. Clin Allergy Immunol. 2007;20:93-101.
113.
Patou J, Gevaert P, Van Zele T, Holtappels G, van Cauwenberge P, Bachert C. Staphylococcus aureus enterotoxin B, protein A, and lipoteichoic acid stimulations in nasal polyps. J Allergy Clin Immunol. 2008 Jan;121(1):110-5. DOI: 10.1016/j.jaci.2007.08.059 External link
114.
Patou J, Holtappels G, Affleck K, Gevaert P, Perez-Novo C, Van Cauwenberge P, Bachert C. Enhanced release of IgE-dependent early phase mediators from nasal polyp tissue. J Inflamm (Lond). 2009;6:11. DOI: 10.1186/1476-9255-6-11 External link
115.
Bachert C, Gevaert P, Holtappels G, Johansson SG, van Cauwenberge P. Total and specific IgE in nasal polyps is related to local eosinophilic inflammation. J Allergy Clin Immunol. 2001 Apr;107(4):607-14. DOI: 10.1067/mai.2001.112374 External link
116.
Vlaminck S, Vauterin T, Hellings PW, Jorissen M, Acke F, Van Cauwenberge P, Bachert C, Gevaert P. The importance of local eosinophilia in the surgical outcome of chronic rhinosinusitis: a 3-year prospective observational study. Am J Rhinol Allergy. 2014 May-Jun;28(3):260-4. DOI: 10.2500/ajra.2014.28.4024 External link
117.
Meyer JE, Bartels J, Görögh T, Sticherling M, Rudack C, Ross DA, Maune S. The role of RANTES in nasal polyposis. Am J Rhinol. 2005 Jan-Feb;19(1):15-20.
118.
Bartels J, Maune S, Meyer JE, Kulke R, Schlüter C, Röwert J, Christophers E, Schröder JM. Increased eotaxin-mRNA expression in non-atopic and atopic nasal polyps: comparison to RANTES and MCP-3 expression. Rhinology. 1997 Dec;35(4):171-4.
119.
Jahnsen FL, Haye R, Gran E, Brandtzaeg P, Johansen FE. Glucocorticosteroids inhibit mRNA expression for eotaxin, eotaxin-2, and monocyte-chemotactic protein-4 in human airway inflammation with eosinophilia. J Immunol. 1999 Aug;163(3):1545-51.
120.
Simon HU, Yousefi S, Schranz C, Schapowal A, Bachert C, Blaser K. Direct demonstration of delayed eosinophil apoptosis as a mechanism causing tissue eosinophilia. J Immunol. 1997 Apr;158(8):3902-8.
121.
Foreman A, Holtappels G, Psaltis AJ, Jervis-Bardy J, Field J, Wormald PJ, Bachert C. Adaptive immune responses in Staphylococcus aureus biofilm-associated chronic rhinosinusitis. Allergy. 2011 Nov;66(11):1449-56. DOI: 10.1111/j.1398-9995.2011.02678.x External link
122.
Schleimer RP, Bochner BS. The effects of glucocorticoids on human eosinophils. J Allergy Clin Immunol. 1994 Dec;94(6 Pt 2):1202-13. DOI: 10.1016/0091-6749(94)90333-6 External link
123.
Van Zele T, Gevaert P, Holtappels G, Beule A, Wormald PJ, Mayr S, Hens G, Hellings P, Ebbens FA, Fokkens W, Van Cauwenberge P, Bachert C. Oral steroids and doxycycline: two different approaches to treat nasal polyps. J Allergy Clin Immunol. 2010 May;125(5):1069-76. DOI: 10.1016/j.jaci.2010.02.020 External link
124.
Gevaert P, Bachert C, Holtappels G, Novo CP, Van der Heyden J, Fransen L, Depraetere S, Walter H, van Cauwenberge P, Tavernier J. Enhanced soluble interleukin-5 receptor alpha expression in nasal polyposis. Allergy. 2003 May;58(5):371-9. DOI: 10.1034/j.1398-9995.2003.00110.x External link
125.
Derycke L, Zhang N, Holtappels G, Dutré T, Bachert C. IL-17A as a regulator of neutrophil survival in nasal polyp disease of patients with and without cystic fibrosis. J Cyst Fibros. 2012 May;11(3):193-200. DOI: 10.1016/j.jcf.2011.11.007 External link
126.
Katotomichelakis M, Tantilipikorn P, Holtappels G, De Ruyck N, Feng L, Van Zele T, Muangsomboon S, Jareonchasri P, Bunnag C, Danielides V, Cuvelier CA, Hellings PW, Bachert C, Zhang N. Inflammatory patterns in upper airway disease in the same geographical area may change over time. Am J Rhinol Allergy. 2013 Sep-Oct;27(5):354-60. DOI: 10.2500/ajra.2013.27.3922 External link
127.
Serhan CN, Chiang N. Resolution phase lipid mediators of inflammation: agonists of resolution. Curr Opin Pharmacol. 2013 Aug;13(4):632-40. DOI: 10.1016/j.coph.2013.05.012 External link
128.
Van Bruaene N, Perez-Novo C, Van Crombruggen K, De Ruyck N, Holtappels G, Van Cauwenberge P, Gevaert P, Bachert C. Inflammation and remodelling patterns in early stage chronic rhinosinusitis. Clin Exp Allergy. 2012 Jun;42(6):883-90. DOI: 10.1111/j.1365-2222.2011.03898.x External link
129.
Abreu NA, Nagalingam NA, Song Y, Roediger FC, Pletcher SD, Goldberg AN, Lynch SV. Sinus microbiome diversity depletion and Corynebacterium tuberculostearicum enrichment mediates rhinosinusitis. Sci Transl Med. 2012 Sep;4(151):151ra124. DOI: 10.1126/scitranslmed.3003783 External link
130.
Ba L, Zhang N, Meng J, Zhang J, Lin P, Zhou P, Liu S, Bachert C. The association between bacterial colonization and inflammatory pattern in Chinese chronic rhinosinusitis patients with nasal polyps. Allergy. 2011 Oct;66(10):1296-303. DOI: 10.1111/j.1398-9995.2011.02637.x External link
131.
Heikkinen T, Järvinen A. The common cold. Lancet. 2003 Jan;361(9351):51-9. DOI: 10.1016/S0140-6736(03)12162-9 External link
132.
Johnston SL, Pattemore PK, Sanderson G, Smith S, Lampe F, Josephs L, Symington P, O'Toole S, Myint SH, Tyrrell DA. Community study of role of viral infections in exacerbations of asthma in 9-11 year old children. BMJ. 1995 May;310(6989):1225-9. DOI: 10.1136/bmj.310.6989.1225 External link
133.
Nicholson KG, Kent J, Ireland DC. Respiratory viruses and exacerbations of asthma in adults. BMJ. 1993 Oct;307(6910):982-6. DOI: 10.1136/bmj.307.6910.982 External link
134.
Corne JM, Marshall C, Smith S, Schreiber J, Sanderson G, Holgate ST, Johnston SL. Frequency, severity, and duration of rhinovirus infections in asthmatic and non-asthmatic individuals: a longitudinal cohort study. Lancet. 2002 Mar;359(9309):831-4. DOI: 10.1016/S0140-6736(02)07953-9 External link
135.
Message SD, Laza-Stanca V, Mallia P, Parker HL, Zhu J, Kebadze T, Contoli M, Sanderson G, Kon OM, Papi A, Jeffery PK, Stanciu LA, Johnston SL. Rhinovirus-induced lower respiratory illness is increased in asthma and related to virus load and Th1/2 cytokine and IL-10 production. Proc Natl Acad Sci USA. 2008 Sep;105(36):13562-7. DOI: 10.1073/pnas.0804181105 External link
136.
Edwards MR, Regamey N, Vareille M, Kieninger E, Gupta A, Shoemark A, Saglani S, Sykes A, Macintyre J, Davies J, Bossley C, Bush A, Johnston SL. Impaired innate interferon induction in severe therapy resistant atopic asthmatic children. Mucosal Immunol. 2013 Jul;6(4):797-806. DOI: 10.1038/mi.2012.118 External link
137.
Busse WW, Morgan WJ, Gergen PJ, Mitchell HE, Gern JE, Liu AH, Gruchalla RS, Kattan M, Teach SJ, Pongracic JA, Chmiel JF, Steinbach SF, Calatroni A, Togias A, Thompson KM, Szefler SJ, Sorkness CA. Randomized trial of omalizumab (anti-IgE) for asthma in inner-city children. N Engl J Med. 2011 Mar;364(11):1005-15. DOI: 10.1056/NEJMoa1009705 External link
138.
Wang X, Zhang N, Glorieux S, Holtappels G, Vaneechoutte M, Krysko O, Zhang L, Han D, Nauwynck HJ, Bachert C. Herpes simplex virus type 1 infection facilitates invasion of Staphylococcus aureus into the nasal mucosa and nasal polyp tissue. PLoS ONE. 2012;7(6):e39875. DOI: 10.1371/journal.pone.0039875 External link
139.
Corriveau MN, Zhang N, Holtappels G, Van Roy N, Bachert C. Detection of Staphylococcus aureus in nasal tissue with peptide nucleic acid-fluorescence in situ hybridization. Am J Rhinol Allergy. 2009 Sep-Oct;23(5):461-5. DOI: 10.2500/ajra.2009.23.3367 External link
140.
Sachse F, Becker K, von Eiff C, Metze D, Rudack C. Staphylococcus aureus invades the epithelium in nasal polyposis and induces IL-6 in nasal epithelial cells in vitro. Allergy. 2010 Nov;65(11):1430-7. DOI: 10.1111/j.1398-9995.2010.02381.x External link
141.
Van Zele T, Vaneechoutte M, Holtappels G, Gevaert P, van Cauwenberge P, Bachert C. Detection of enterotoxin DNA in Staphylococcus aureus strains obtained from the middle meatus in controls and nasal polyp patients. Am J Rhinol. 2008 May-Jun;22(3):223-7. DOI: 10.2500/ajr.2008.22.3161 External link
142.
Marone G, editor. Superantigens and Superallergens. Basel: Karger; 2007.
143.
Ziegler C, Goldmann O, Hobeika E, Geffers R, Peters G, Medina E. The dynamics of T cells during persistent Staphylococcus aureus infection: from antigen-reactivity to in vivo anergy. EMBO Mol Med. 2011 Nov;3(11):652-66. DOI: 10.1002/emmm.201100173 External link
144.
Herz U, Rückert R, Wollenhaupt K, Tschernig T, Neuhaus-Steinmetz U, Pabst R, Renz H. Airway exposure to bacterial superantigen (SEB) induces lymphocyte-dependent airway inflammation associated with increased airway responsiveness--a model for non-allergic asthma. Eur J Immunol. 1999 Mar;29(3):1021-31. DOI: 10.1002/(SICI)1521-4141(199903)29:03<1021::AID-IMMU1021>3.0.CO;2-3 External link
145.
Hellings PW, Hens G, Meyts I, Bullens D, Vanoirbeek J, Gevaert P, Jorissen M, Ceuppens JL, Bachert C. Aggravation of bronchial eosinophilia in mice by nasal and bronchial exposure to Staphylococcus aureus enterotoxin B. Clin Exp Allergy. 2006 Aug;36(8):1063-71. DOI: 10.1111/j.1365-2222.2006.02527.x External link
146.
Huvenne W, Callebaut I, Plantinga M, Vanoirbeek JA, Krysko O, Bullens DM, Gevaert P, Van Cauwenberge P, Lambrecht BN, Ceuppens JL, Bachert C, Hellings PW. Staphylococcus aureus enterotoxin B facilitates allergic sensitization in experimental asthma. Clin Exp Allergy. 2010 Jul;40(7):1079-90. DOI: 10.1111/j.1365-2222.2010.03464.x External link
147.
Huvenne W, Callebaut I, Reekmans K, Hens G, Bobic S, Jorissen M, Bullens DM, Ceuppens JL, Bachert C, Hellings PW. Staphylococcus aureus enterotoxin B augments granulocyte migration and survival via airway epithelial cell activation. Allergy. 2010 Aug;65(8):1013-20. DOI: 10.1111/j.1398-9995.2009.02313.x External link
148.
Murakami S, Iwaki D, Mitsuzawa H, Sano H, Takahashi H, Voelker DR, Akino T, Kuroki Y. Surfactant protein A inhibits peptidoglycan-induced tumor necrosis factor-alpha secretion in U937 cells and alveolar macrophages by direct interaction with toll-like receptor 2. J Biol Chem. 2002 Mar;277(9):6830-7. DOI: 10.1074/jbc.M106671200 External link
149.
Hofer MF, Lester MR, Schlievert PM, Leung DY. Upregulation of IgE synthesis by staphylococcal toxic shock syndrome toxin-1 in peripheral blood mononuclear cells from patients with atopic dermatitis. Clin Exp Allergy. 1995 Dec;25(12):1218-27. DOI: 10.1111/j.1365-2222.1995.tb03046.x External link
150.
Hofer MF, Harbeck RJ, Schlievert PM, Leung DY. Staphylococcal toxins augment specific IgE responses by atopic patients exposed to allergen. J Invest Dermatol. 1999 Feb;112(2):171-6. DOI: 10.1046/j.1523-1747.1999.00492.x External link
151.
Gevaert P, Holtappels G, Johansson SG, Cuvelier C, Cauwenberge P, Bachert C. Organization of secondary lymphoid tissue and local IgE formation to Staphylococcus aureus enterotoxins in nasal polyp tissue. Allergy. 2005 Jan;60(1):71-9. DOI: 10.1111/j.1398-9995.2004.00621.x External link
152.
Bachert C, van Steen K, Zhang N, Holtappels G, Cattaert T, Maus B, Buhl R, Taube C, Korn S, Kowalski M, Bousquet J, Howarth P. Specific IgE against Staphylococcus aureus enterotoxins: an independent risk factor for asthma. J Allergy Clin Immunol. 2012 Aug;130(2):376-81.e8. DOI: 10.1016/j.jaci.2012.05.012 External link
153.
Tomassen P, Jarvis D, Newson R, Van Ree R, Forsberg B, Howarth P, Janson C, Kowalski ML, Krämer U, Matricardi PM, Middelveld RJ, Todo-Bom A, Toskala E, Thilsing T, Brożek G, Van Drunen C, Burney P, Bachert C. Staphylococcus aureus enterotoxin-specific IgE is associated with asthma in the general population: a GA(2)LEN study. Allergy. 2013 Oct;68(10):1289-97. DOI: 10.1111/all.12230 External link
154.
Song WJ, Chang YS, Lim MK, Yun EH, Kim SH, Kang HR, Park HW, Tomassen P, Choi MH, Min KU, Cho SH, Bachert C. Staphylococcal enterotoxin sensitization in a community-based population: a potential role in adult-onset asthma. Clin Exp Allergy. 2014 Apr;44(4):553-62. DOI: 10.1111/cea.12239 External link
155.
Semic-Jusufagic A, Bachert C, Gevaert P, Holtappels G, Lowe L, Woodcock A, Simpson A, Custovic A. Staphylococcus aureus sensitization and allergic disease in early childhood: population-based birth cohort study. J Allergy Clin Immunol. 2007 Apr;119(4):930-6. DOI: 10.1016/j.jaci.2006.12.639 External link
156.
Hollams EM, Hales BJ, Bachert C, Huvenne W, Parsons F, de Klerk NH, Serralha M, Holt BJ, Ahlstedt S, Thomas WR, Sly PD, Holt PG. Th2-associated immunity to bacteria in teenagers and susceptibility to asthma. Eur Respir J. 2010 Sep;36(3):509-16. DOI: 10.1183/09031936.00184109 External link
157.
Schubert MS. Allergic fungal sinusitis. Clin Rev Allergy Immunol. 2006 Jun;30(3):205-16. DOI: 10.1385/CRIAI:30:3:205 External link
158.
Schubert MS. Allergic fungal sinusitis: pathophysiology, diagnosis and management. Med Mycol. 2009;47 Suppl 1:S324-30. DOI: 10.1080/13693780802314809 External link
159.
Dutre T, Al Dousary S, Zhang N, Bachert C. Allergic fungal rhinosinusitis-more than a fungal disease? J Allergy Clin Immunol. 2013 Aug;132(2):487-9.e1. DOI: 10.1016/j.jaci.2013.02.040 External link
160.
Scadding GK, Durham SR, Mirakian R, Jones NS, Drake-Lee AB, Ryan D, Dixon TA, Huber PA, Nasser SM; British Society for Allergy and Clinical Immunology. BSACI guidelines for the management of rhinosinusitis and nasal polyposis. Clin Exp Allergy. 2008 Feb;38(2):260-75. DOI: 10.1111/j.1365-2222.2007.02889.x External link
161.
Accomazzo MR, Rovati GE, Viganò T, Hernandez A, Bonazzi A, Bolla M, Fumagalli F, Viappiani S, Galbiati E, Ravasi S, Albertoni C, Di Luca M, Caputi A, Zannini P, Chiesa G, Villa AM, Doglia SM, Folco G, Nicosia S. Leukotriene D4-induced activation of smooth-muscle cells from human bronchi is partly Ca2+-independent. Am J Respir Crit Care Med. 2001 Jan;163(1):266-72. DOI: 10.1164/ajrccm.163.1.9912019 External link
162.
Bandeira-Melo C, Weller PF. Eosinophils and cysteinyl leukotrienes. Prostaglandins Leukot Essent Fatty Acids. 2003 Aug-Sep;69(2-3):135-43. DOI: 10.1016/S0952-3278(03)00074-7 External link
163.
Roca-Ferrer J, Garcia-Garcia FJ, Pereda J, Perez-Gonzalez M, Pujols L, Alobid I, Mullol J, Picado C. Reduced expression of COXs and production of prostaglandin E(2) in patients with nasal polyps with or without aspirin-intolerant asthma. J Allergy Clin Immunol. 2011 Jul;128(1):66-72.e1. DOI: 10.1016/j.jaci.2011.01.065 External link
164.
Pérez-Novo CA, Claeys C, Van Cauwenberge P, Bachert C. Expression of eicosanoid receptors subtypes and eosinophilic inflammation: implication on chronic rhinosinusitis. Respir Res. 2006;7:75. DOI: 10.1186/1465-9921-7-75 External link
165.
Liu CM, Hong CY, Shun CT, Hsiao TY, Wang CC, Wang JS, Hsiao M, Lin SK. Inducible cyclooxygenase and interleukin 6 gene expressions in nasal polyp fibroblasts: possible implication in the pathogenesis of nasal polyposis. Arch Otolaryngol Head Neck Surg. 2002 Aug;128(8):945-51. DOI: 10.1001/archotol.128.8.945 External link
166.
Okano M, Fujiwara T, Yamamoto M, Sugata Y, Matsumoto R, Fukushima K, Yoshino T, Shimizu K, Eguchi N, Kiniwa M, Urade Y, Nishizaki K. Role of prostaglandin D2 and E2 terminal synthases in chronic rhinosinusitis. Clin Exp Allergy. 2006 Aug;36(8):1028-38. DOI: 10.1111/j.1365-2222.2006.02528.x External link
167.
Yamamoto M, Okano M, Fujiwara T, Kariya S, Higaki T, Nagatsuka H, Tsujigiwa H, Yamada M, Yoshino T, Urade Y, Nishizaki K. Expression and characterization of PGD2 receptors in chronic rhinosinusitis: modulation of DP and CRTH2 by PGD2. Int Arch Allergy Immunol. 2009;148(2):127-36. DOI: 10.1159/000155743 External link
168.
Sanak M, Levy BD, Clish CB, Chiang N, Gronert K, Mastalerz L, Serhan CN, Szczeklik A. Aspirin-tolerant asthmatics generate more lipoxins than aspirin-intolerant asthmatics. Eur Respir J. 2000 Jul;16(1):44-9. DOI: 10.1034/j.1399-3003.2000.16a08.x External link
169.
Videler WJ, Badia L, Harvey RJ, Gane S, Georgalas C, van der Meulen FW, Menger DJ, Lehtonen MT, Toppila-Salmi SK, Vento SI, Hytönen M, Hellings PW, Kalogjera L, Lund VJ, Scadding G, Mullol J, Fokkens WJ. Lack of efficacy of long-term, low-dose azithromycin in chronic rhinosinusitis: a randomized controlled trial. Allergy. 2011 Nov;66(11):1457-68. DOI: 10.1111/j.1398-9995.2011.02693.x External link
170.
Cervin A, Wallwork B. Efficacy and safety of long-term antibiotics (macrolides) for the treatment of chronic rhinosinusitis. Curr Allergy Asthma Rep. 2014 Mar;14(3):416. DOI: 10.1007/s11882-013-0416-2 External link
171.
Coles CL, Mabula K, Seidman JC, Levens J, Mkocha H, Munoz B, Mfinanga SG, West S. Mass distribution of azithromycin for trachoma control is associated with increased risk of azithromycin-resistant Streptococcus pneumoniae carriage in young children 6 months after treatment. Clin Infect Dis. 2013 Jun;56(11):1519-26. DOI: 10.1093/cid/cit137 External link
172.
Schafer T, Schnoor M, Wagenmann M, Klimek L, Bachert C. Therapeutic Index (TIX) for intranasal corticosteroids in the treatment of allergic rhinitis. Rhinology. 2011 Aug;49(3):272-80. DOI: 10.4193/Rhino10.170 External link
173.
Pérez-Novo CA, Kowalski ML, Kuna P, Ptasinska A, Holtappels G, van Cauwenberge P, Gevaert P, Johannson S, Bachert C. Aspirin sensitivity and IgE antibodies to Staphylococcus aureus enterotoxins in nasal polyposis: studies on the relationship. Int Arch Allergy Immunol. 2004 Mar;133(3):255-60. DOI: 10.1159/000076832 External link
174.
Klimek L, Dollner R, Pfaar O, Mullol J. Aspirin desensitization: useful treatment for chronic rhinosinusitis with nasal polyps (CRSwNP) in aspirin-exacerbated respiratory disease (AERD)? Curr Allergy Asthma Rep. 2014 Jun;14(6):441. DOI: 10.1007/s11882-014-0441-9 External link
175.
Casale TB, Condemi J, LaForce C, Nayak A, Rowe M, Watrous M, McAlary M, Fowler-Taylor A, Racine A, Gupta N, Fick R, Della Cioppa G; Omalizumab Seasonal Allergic Rhinitis Trail Group. Effect of omalizumab on symptoms of seasonal allergic rhinitis: a randomized controlled trial. JAMA. 2001 Dec;286(23):2956-67. DOI: 10.1001/jama.286.23.2956 External link
176.
Donovan R, Johansson SG, Bennich H, Soothill JF. Immunoglobulins in nasal polyp fluid. Int Arch Allergy Appl Immunol. 1970;37(2):154-66. DOI: 10.1159/000230229 External link
177.
Verbruggen K, Van Cauwenberge P, Bachert C. Anti-IgE for the treatment of allergic rhinitis--and eventually nasal polyps? Int Arch Allergy Immunol. 2009;148(2):87-98. DOI: 10.1159/000155739 External link
178.
Pinto JM, Mehta N, DiTineo M, Wang J, Baroody FM, Naclerio RM. A randomized, double-blind, placebo-controlled trial of anti-IgE for chronic rhinosinusitis. Rhinology. 2010 Sep;48(3):318-24. DOI: 10.4193/Rhin09.144 External link
179.
Holgate S, Casale T, Wenzel S, Bousquet J, Deniz Y, Reisner C. The anti-inflammatory effects of omalizumab confirm the central role of IgE in allergic inflammation. J Allergy Clin Immunol. 2005 Mar;115(3):459-65. DOI: 10.1016/j.jaci.2004.11.053 External link
180.
Gevaert P, Calus L, Van Zele T, Blomme K, De Ruyck N, Bauters W, Hellings P, Brusselle G, De Bacquer D, van Cauwenberge P, Bachert C. Omalizumab is effective in allergic and nonallergic patients with nasal polyps and asthma. J Allergy Clin Immunol. 2013 Jan;131(1):110-6.e1. DOI: 10.1016/j.jaci.2012.07.047 External link
181.
Garcia G, Magnan A, Chiron R, Contin-Bordes C, Berger P, Taillé C, Devouassoux G, de Blay F, Couderc LJ, Didier A, O'Callaghan DS, Girodet PO, Bourdeix I, Le Gros V, Humbert M. A proof-of-concept, randomized, controlled trial of omalizumab in patients with severe, difficult-to-control, nonatopic asthma. Chest. 2013 Aug;144(2):411-9. DOI: 10.1378/chest.12-1961 External link
182.
Vennera Mdel C, Picado C, Mullol J, Alobid I, Bernal-Sprekelsen M. Efficacy of omalizumab in the treatment of nasal polyps. Thorax. 2011 Sep;66(9):824-5. DOI: 10.1136/thx.2010.152835 External link
183.
Long A, Rahmaoui A, Rothman KJ, Guinan E, Eisner M, Bradley MS, Iribarren C, Chen H, Carrigan G, Rosén K, Szefler SJ. Incidence of malignancy in patients with moderate-to-severe asthma treated with or without omalizumab. J Allergy Clin Immunol. 2014 Sep;134(3):560-7. DOI: 10.1016/j.jaci.2014.02.007 External link
184.
Gevaert P, Lang-Loidolt D, Lackner A, Stammberger H, Staudinger H, Van Zele T, Holtappels G, Tavernier J, van Cauwenberge P, Bachert C. Nasal IL-5 levels determine the response to anti-IL-5 treatment in patients with nasal polyps. J Allergy Clin Immunol. 2006 Nov;118(5):1133-41. DOI: 10.1016/j.jaci.2006.05.031 External link
185.
Wenzel S, Ford L, Pearlman D, Spector S, Sher L, Skobieranda F, Wang L, Kirkesseli S, Rocklin R, Bock B, Hamilton J, Ming JE, Radin A, Stahl N, Yancopoulos GD, Graham N, Pirozzi G. Dupilumab in persistent asthma with elevated eosinophil levels. N Engl J Med. 2013 Jun;368(26):2455-66. DOI: 10.1056/NEJMoa1304048 External link
186.
Bermúdez-Humarán LG, Aubry C, Motta JP, Deraison C, Steidler L, Vergnolle N, Chatel JM, Langella P. Engineering lactococci and lactobacilli for human health. Curr Opin Microbiol. 2013 Jun;16(3):278-83. DOI: 10.1016/j.mib.2013.06.002 External link
187.
Krug N, Hohlfeld JM, Kirsten AM, Kornmann O, Beeh KM, Kappeler D, Korn S, Ignatenko S, Timmer W, Rogon C, Zeitvogel J, Zhang N, Bille J, Homburg U, Turowska A, Bachert C, Werfel T, Buhl R, Renz J, Garn H, Renz H. Allergen-induced asthmatic responses modified by a GATA3-specific DNAzyme. N Engl J Med. 2015 May;372(21):1987-95. DOI: 10.1056/NEJMoa1411776 External link
188.
Kerkhoff C, Sorg C, Tandon NN, Nacken W. Interaction of S100A8/S100A9-arachidonic acid complexes with the scavenger receptor CD36 may facilitate fatty acid uptake by endothelial cells. Biochemistry. 2001 Jan;40(1):241-8. DOI: 10.1021/bi001791k External link
189.
Ghavami S, Rashedi I, Dattilo BM, Eshraghi M, Chazin WJ, Hashemi M, Wesselborg S, Kerkhoff C, Los M. S100A8/A9 at low concentration promotes tumor cell growth via RAGE ligation and MAP kinase-dependent pathway. J Leukoc Biol. 2008 Jun;83(6):1484-92. DOI: 10.1189/jlb.0607397 External link
190.
Boyd JH, Kan B, Roberts H, Wang Y, Walley KR. S100A8 and S100A9 mediate endotoxin-induced cardiomyocyte dysfunction via the receptor for advanced glycation end products. Circ Res. 2008 May;102(10):1239-46. DOI: 10.1161/CIRCRESAHA.107.167544 External link
191.
Bryborn M, Adner M, Cardell LO. Psoriasin, one of several new proteins identified in nasal lavage fluid from allergic and non-allergic individuals using 2-dimensional gel electrophoresis and mass spectrometry. Respir Res. 2005;6:118. DOI: 10.1186/1465-9921-6-118 External link
192.
Leclerc E, Fritz G, Vetter SW, Heizmann CW. Binding of S100 proteins to RAGE: an update. Biochim Biophys Acta. 2009 Jun;1793(6):993-1007. DOI: 10.1016/j.bbamcr.2008.11.016 External link
193.
Fritz G. RAGE: a single receptor fits multiple ligands. Trends Biochem Sci. 2011 Dec;36(12):625-32. DOI: 10.1016/j.tibs.2011.08.008 External link
194.
Lee HM, Kang HJ, Woo JS, Chae SW, Lee SH, Hwang SJ. Upregulation of surfactant protein A in chronic rhinosinusitis. Laryngoscope. 2006 Feb;116(2):328-30. DOI: 10.1097/01.mlg.0000194223.22763.5f External link
195.
Wang X, Zhao C, Liu M. Expression and significance of surfactant A in nasal polyps of chronic rhinosinusitis. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Jul;24(14):652-4.
196.
Woodworth BA, Wood R, Baatz JE, Schlosser RJ. Sinonasal surfactant protein A1, A2, and D gene expression in cystic fibrosis: a preliminary report. Otolaryngol Head Neck Surg. 2007 Jul;137(1):34-8. DOI: 10.1016/j.otohns.2007.01.025 External link
197.
Skinner ML, Schlosser RJ, Lathers D, Neal JG, Woodworth BA, Hall J, Newton DA, Baatz JE. Innate and adaptive mediators in cystic fibrosis and allergic fungal rhinosinusitis. Am J Rhinol. 2007 Sep-Oct;21(5):538-41. DOI: 10.2500/ajr.2007.21.3070 External link
198.
Ooi EH, Wormald PJ, Carney AS, James CL, Tan LW. Surfactant protein d expression in chronic rhinosinusitis patients and immune responses in vitro to Aspergillus and alternaria in a nasal explant model. Laryngoscope. 2007 Jan;117(1):51-7. DOI: 10.1097/01.mlg.0000243196.75418.6f External link
199.
Guillot L, Balloy V, McCormack FX, Golenbock DT, Chignard M, Si-Tahar M. Cutting edge: the immunostimulatory activity of the lung surfactant protein-A involves Toll-like receptor 4. J Immunol. 2002 Jun;168(12):5989-92. DOI: 10.4049/jimmunol.168.12.5989 External link
200.
Henning LN, Azad AK, Parsa KV, Crowther JE, Tridandapani S, Schlesinger LS. Pulmonary surfactant protein A regulates TLR expression and activity in human macrophages. J Immunol. 2008 Jun;180(12):7847-58. DOI: 10.4049/jimmunol.180.12.7847 External link
201.
Ohya M, Nishitani C, Sano H, Yamada C, Mitsuzawa H, Shimizu T, Saito T, Smith K, Crouch E, Kuroki Y. Human pulmonary surfactant protein D binds the extracellular domains of Toll-like receptors 2 and 4 through the carbohydrate recognition domain by a mechanism different from its binding to phosphatidylinositol and lipopolysaccharide. Biochemistry. 2006 Jul;45(28):8657-64. DOI: 10.1021/bi060176z External link
202.
Yamada C, Sano H, Shimizu T, Mitsuzawa H, Nishitani C, Himi T, Kuroki Y. Surfactant protein A directly interacts with TLR4 and MD-2 and regulates inflammatory cellular response. Importance of supratrimeric oligomerization. J Biol Chem. 2006 Aug;281(31):21771-80. DOI: 10.1074/jbc.M513041200 External link
203.
Kalfa VC, Spector SL, Ganz T, Cole AM. Lysozyme levels in the nasal secretions of patients with perennial allergic rhinitis and recurrent sinusitis. Ann Allergy Asthma Immunol. 2004 Sep;93(3):288-92. DOI: 10.1016/S1081-1206(10)61503-7 External link
204.
Bascom R, Pipkorn U, Proud D, Dunnette S, Gleich GJ, Lichtenstein LM, Naclerio RM. Major basic protein and eosinophil-derived neurotoxin concentrations in nasal-lavage fluid after antigen challenge: effect of systemic corticosteroids and relationship to eosinophil influx. J Allergy Clin Immunol. 1989 Sep;84(3):338-46. DOI: 10.1016/0091-6749(89)90418-1 External link
205.
Yang D, Chen Q, Su SB, Zhang P, Kurosaka K, Caspi RR, Michalek SM, Rosenberg HF, Zhang N, Oppenheim JJ. Eosinophil-derived neurotoxin acts as an alarmin to activate the TLR2-MyD88 signal pathway in dendritic cells and enhances Th2 immune responses. J Exp Med. 2008 Jan;205(1):79-90. DOI: 10.1084/jem.20062027 External link
206.
Bilodeau L, Boulay ME, Prince P, Boisvert P, Boulet LP. Comparative clinical and airway inflammatory features of asthmatics with or without polyps. Rhinology. 2010 Dec;48(4):420-5. DOI: 10.4193/Rhino09.095 External link
207.
Nakagawa T, Yamane H, Shigeta T, Takashima T, Nakai Y. Interaction between fibronectin and eosinophils in the growth of nasal polyps. Laryngoscope. 1999 Apr;109(4):557-61. DOI: 10.1097/00005537-199904000-00007 External link
208.
Sobol SE, Christodoulopoulos P, Manoukian JJ, Hauber HP, Frenkiel S, Desrosiers M, Fukakusa M, Schloss MD, Hamid Q. Cytokine profile of chronic sinusitis in patients with cystic fibrosis. Arch Otolaryngol Head Neck Surg. 2002 Nov;128(11):1295-8. DOI: 10.1001/archotol.128.11.1295 External link
209.
Bachert C, Zhang N. Chronic rhinosinusitis and asthma: novel understanding of the role of IgE 'above atopy'. J Intern Med. 2012 Aug;272(2):133-43. DOI: 10.1111/j.1365-2796.2012.02559.x External link
210.
Liu Y, Zhang S, Li DW, Jiang SJ. Efficacy of anti-interleukin-5 therapy with mepolizumab in patients with asthma: a meta-analysis of randomized placebo-controlled trials. PLoS ONE. 2013;8(3):e59872. DOI: 10.1371/journal.pone.0059872 External link
211.
Castro M, Mathur S, Hargreave F, Boulet LP, Xie F, Young J, Wilkins HJ, Henkel T, Nair P; Res-5-0010 Study Group. Reslizumab for poorly controlled, eosinophilic asthma: a randomized, placebo-controlled study. Am J Respir Crit Care Med. 2011 Nov;184(10):1125-32. DOI: 10.1164/rccm.201103-0396OC External link
212.
Laviolette M, Gossage DL, Gauvreau G, Leigh R, Olivenstein R, Katial R, Busse WW, Wenzel S, Wu Y, Datta V, Kolbeck R, Molfino NA. Effects of benralizumab on airway eosinophils in asthmatic patients with sputum eosinophilia. J Allergy Clin Immunol. 2013 Nov;132(5):1086-1096.e5. DOI: 10.1016/j.jaci.2013.05.020 External link
213.
ClinicalTrialsRegister.eu [Internet]. London: European Medicines Agency; c1995-2015. Available from: https://www.clinicaltrialsregister.eu External link
214.
Pelaia G, Vatrella A, Maselli R. The potential of biologics for the treatment of asthma. Nat Rev Drug Discov. 2012 Dec;11(12):958-72. DOI: 10.1038/nrd3792 External link
215.
Steinke JW. Anti-interleukin-4 therapy. Immunol Allergy Clin North Am. 2004 Nov;24(4):599-614, vi. DOI: 10.1016/j.iac.2004.06.008 External link
216.
Slager RE, Otulana BA, Hawkins GA, Yen YP, Peters SP, Wenzel SE, Meyers DA, Bleecker ER. IL-4 receptor polymorphisms predict reduction in asthma exacerbations during response to an anti-IL-4 receptor alpha antagonist. J Allergy Clin Immunol. 2012 Aug;130(2):516-22.e4. DOI: 10.1016/j.jaci.2012.03.030 External link
217.
Oh CK, Leigh R, McLaurin KK, Kim K, Hultquist M, Molfino NA. A randomized, controlled trial to evaluate the effect of an anti-interleukin-9 monoclonal antibody in adults with uncontrolled asthma. Respir Res. 2013;14:93. DOI: 10.1186/1465-9921-14-93 External link
218.
Busse WW, Holgate S, Kerwin E, Chon Y, Feng J, Lin J, Lin SL. Randomized, double-blind, placebo-controlled study of brodalumab, a human anti-IL-17 receptor monoclonal antibody, in moderate to severe asthma. Am J Respir Crit Care Med. 2013 Dec;188(11):1294-302. DOI: 10.1164/rccm.201212-2318OC External link
219.
Piper E, Brightling C, Niven R, Oh C, Faggioni R, Poon K, She D, Kell C, May RD, Geba GP, Molfino NA. A phase II placebo-controlled study of tralokinumab in moderate-to-severe asthma. Eur Respir J. 2013 Feb;41(2):330-8. DOI: 10.1183/09031936.00223411 External link
220.
Gauvreau GM, Boulet LP, Cockcroft DW, Fitzgerald JM, Carlsten C, Davis BE, Deschesnes F, Duong M, Durn BL, Howie KJ, Hui L, Kasaian MT, Killian KJ, Strinich TX, Watson RM, Y N, Zhou S, Raible D, O'Byrne PM. Effects of interleukin-13 blockade on allergen-induced airway responses in mild atopic asthma. Am J Respir Crit Care Med. 2011 Apr;183(8):1007-14. DOI: 10.1164/rccm.201008-1210OC External link
221.
Noonan M, Korenblat P, Mosesova S, Scheerens H, Arron JR, Zheng Y, Putnam WS, Parsey MV, Bohen SP, Matthews JG. Dose-ranging study of lebrikizumab in asthmatic patients not receiving inhaled steroids. J Allergy Clin Immunol. 2013 Sep;132(3):567-74. DOI: 10.1016/j.jaci.2013.03.051 External link
222.
Scheerens H, Arron JR, Zheng Y, Putnam WS, Erickson RW, Choy DF, Harris JM, Lee J, Jarjour NN, Matthews JG. The effects of lebrikizumab in patients with mild asthma following whole lung allergen challenge. Clin Exp Allergy. 2014 Jan;44(1):38-46. DOI: 10.1111/cea.12220 External link
223.
Barnes PJ. New therapies for asthma: is there any progress? Trends Pharmacol Sci. 2010 Jul;31(7):335-43. DOI: 10.1016/j.tips.2010.04.009 External link
224.
Taillé C, Poulet C, Marchand-Adam S, Borie R, Dombret MC, Crestani B, Aubier M. Monoclonal Anti-TNF-α Antibodies for Severe Steroid-Dependent Asthma: A Case Series. Open Respir Med J. 2013;7:21-5. DOI: 10.2174/1874306401307010021 External link
225.
Gauvreau GM, O'Byrne PM, Boulet LP, Wang Y, Cockcroft D, Bigler J, FitzGerald JM, Boedigheimer M, Davis BE, Dias C, Gorski KS, Smith L, Bautista E, Comeau MR, Leigh R, Parnes JR. Effects of an anti-TSLP antibody on allergen-induced asthmatic responses. N Engl J Med. 2014 May;370(22):2102-10. DOI: 10.1056/NEJMoa1402895 External link
226.
Neighbour H, Boulet LP, Lemiere C, Sehmi R, Leigh R, Sousa AR, Martin J, Dallow N, Gilbert J, Allen A, Hall D, Nair P. Safety and efficacy of an oral CCR3 antagonist in patients with asthma and eosinophilic bronchitis: a randomized, placebo-controlled clinical trial. Clin Exp Allergy. 2014 Apr;44(4):508-16. DOI: 10.1111/cea.12244 External link
227.
Busse WW, Wenzel SE, Meltzer EO, Kerwin EM, Liu MC, Zhang N, Chon Y, Budelsky AL, Lin J, Lin SL. Safety and efficacy of the prostaglandin D2 receptor antagonist AMG 853 in asthmatic patients. J Allergy Clin Immunol. 2013 Feb;131(2):339-45. DOI: 10.1016/j.jaci.2012.10.013 External link
228.
Nair P, Gaga M, Zervas E, Alagha K, Hargreave FE, O'Byrne PM, Stryszak P, Gann L, Sadeh J, Chanez P; Study Investigators. Safety and efficacy of a CXCR2 antagonist in patients with severe asthma and sputum neutrophils: a randomized, placebo-controlled clinical trial. Clin Exp Allergy. 2012 Jul;42(7):1097-103. DOI: 10.1111/j.1365-2222.2012.04014.x External link
229.
Beeh KM, Kanniess F, Wagner F, Schilder C, Naudts I, Hammann-Haenni A, Willers J, Stocker H, Mueller P, Bachmann MF, Renner WA. The novel TLR-9 agonist QbG10 shows clinical efficacy in persistent allergic asthma. J Allergy Clin Immunol. 2013 Mar;131(3):866-74. DOI: 10.1016/j.jaci.2012.12.1561 External link
230.
ClinicalTrials.gov [Internet]. Bethesda, Maryland: NIH; c1993- [updated May 2014]. Available from: https://clinicaltrials.gov/ External link
231.
Franciosi LG, Diamant Z, Banner KH, Zuiker R, Morelli N, Kamerling IM, de Kam ML, Burggraaf J, Cohen AF, Cazzola M, Calzetta L, Singh D, Spina D, Walker MJ, Page CP. Efficacy and safety of RPL554, a dual PDE3 and PDE4 inhibitor, in healthy volunteers and in patients with asthma or chronic obstructive pulmonary disease: findings from four clinical trials. Lancet Respir Med. 2013 Nov;1(9):714-27. DOI: 10.1016/S2213-2600(13)70187-5 External link
232.
Sel S, Wegmann M, Dicke T, Sel S, Henke W, Yildirim AO, Renz H, Garn H. Effective prevention and therapy of experimental allergic asthma using a GATA-3-specific DNAzyme. J Allergy Clin Immunol. 2008 Apr;121(4):910-6. DOI: 10.1016/j.jaci.2007.12.1175 External link