The composition of house dust mite is critical for mucosal barrier dysfunction and allergic sensitisation

Background House dust mite (HDM) allergens have been reported to increase airway epithelial permeability, thereby facilitating access of allergens and allergic sensitisation. Objectives The authors aimed to understand which biochemical properties of HDM are critical for epithelial immune and barrier responses as well as T helper 2-driven experimental asthma in vivo. Methods Three commercially available HDM extracts were analysed for endotoxin levels, protease and chitinase activities and effects on transepithelial resistance, junctional proteins and pro-inflammatory cytokine release in the bronchial epithelial cell line 16HBE and normal human bronchial cells. Furthermore, the effects on epithelial remodelling and airway inflammation were investigated in a mouse model. Results The different HDM extracts varied extensively in their biochemical properties and induced divergent responses in vitro and in vivo. Importantly, the Greer extract, with the lowest serine protease activity, induced the most pronounced effects on epithelial barrier function and CCL20 release in vitro. In vivo, this extract induced the most profound epithelial E-cadherin delocalisation and increase in CCL20, CCL17 and interleukin 5 levels, accompanied by the most pronounced induction of HDM-specific IgE, goblet cell hyperplasia, eosinophilic inflammation and airway hyper-reactivity. Conclusions This study shows the ability of HDM extracts to alter epithelial immune and barrier responses is related to allergic sensitisation but independent of serine/cysteine protease activity.

[1]  D. Postma,et al.  E-cadherin: gatekeeper of airway mucosa and allergic sensitization. , 2011, Trends in immunology.

[2]  J. Whitsett,et al.  Epithelial EGF receptor signaling mediates airway hyperreactivity and remodeling in a mouse model of chronic asthma. , 2011, American journal of physiology. Lung cellular and molecular physiology.

[3]  John R. Ledford,et al.  Mucosal sensitization to German cockroach involves protease-activated receptor-2 , 2010, Respiratory research.

[4]  I. Heijink,et al.  Epidermal growth factor receptor signalling contributes to house dust mite-induced epithelial barrier dysfunction , 2010, European Respiratory Journal.

[5]  F. Finkelman,et al.  Importance of Cytokines in Murine Allergic Airway Disease and Human Asthma , 2010, The Journal of Immunology.

[6]  Richard Graham Knowles,et al.  House dust mite induces direct airway inflammation in vivo: implications for future disease therapy? , 2009, European Respiratory Journal.

[7]  D. Postma,et al.  Characterisation of cell adhesion in airway epithelial cell types using electric cell–substrate impedance sensing , 2009, European Respiratory Journal.

[8]  H. Grönlund,et al.  The non‐proteolytic house dust mite allergen Der p 2 induce NF‐κB and MAPK dependent activation of bronchial epithelial cells , 2009, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[9]  H. Hammad,et al.  House dust mite allergen induces asthma via Toll-like receptor 4 triggering of airway structural cells , 2009, Nature Medicine.

[10]  Koon-Guan Lee,et al.  Phospholipase Cγ2 Is Critical for Dectin-1-mediated Ca2+ Flux and Cytokine Production in Dendritic Cells* , 2009, Journal of Biological Chemistry.

[11]  M. Wills-Karp,et al.  Innate immune responses of airway epithelium to house dust mite are mediated through beta-glucan-dependent pathways. , 2009, The Journal of allergy and clinical immunology.

[12]  A. Prince,et al.  TLR2-induced calpain cleavage of epithelial junctional proteins facilitates leukocyte transmigration. , 2009, Cell host & microbe.

[13]  Liang Dong,et al.  Different Doses of Lipopolysaccharides Regulate the Lung Inflammation of Asthmatic Mice via TLR4 Pathway in Alveolar Macrophages , 2009, The Journal of asthma : official journal of the Association for the Care of Asthma.

[14]  R. Hegde,et al.  Allergenicity resulting from functional mimicry of a Toll-like receptor complex protein , 2008, Nature.

[15]  N. Bloksma,et al.  Indoleamine 2,3-dioxygenase-dependent tryptophan metabolites contribute to tolerance induction during allergen immunotherapy in a mouse model. , 2008, The Journal of allergy and clinical immunology.

[16]  M. Wills-Karp,et al.  Differences in susceptibility to German cockroach frass and its associated proteases in induced allergic inflammation in mice , 2007, Respiratory research.

[17]  D. Postma,et al.  Down-Regulation of E-Cadherin in Human Bronchial Epithelial Cells Leads to Epidermal Growth Factor Receptor-Dependent Th2 Cell-Promoting Activity1 , 2007, The Journal of Immunology.

[18]  D. Shasby,et al.  PAR2 activation interrupts E-cadherin adhesion and compromises the airway epithelial barrier: protective effect of beta-agonists. , 2006, American journal of physiology. Lung cellular and molecular physiology.

[19]  M. Tamm,et al.  House dust mite major allergens Der p 1 and Der p 5 activate human airway-derived epithelial cells by protease-dependent and protease-independent mechanisms , 2006, Clinical and molecular allergy : CMA.

[20]  R. Homer,et al.  Chitinases and chitinase-like proteins in T(H)2 inflammation and asthma. , 2005, The Journal of allergy and clinical immunology.

[21]  M. Jordana,et al.  House dust mite facilitates ovalbumin-specific allergic sensitization and airway inflammation. , 2005, American journal of respiratory and critical care medicine.

[22]  D. Robinson,et al.  Thymic Stromal Lymphopoietin Expression Is Increased in Asthmatic Airways and Correlates with Expression of Th2-Attracting Chemokines and Disease Severity1 , 2005, The Journal of Immunology.

[23]  F. Shakib,et al.  Proteolytic activity of the house dust mite allergen Der p 1 enhances allergenicity in a mouse inhalation model , 2003, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[24]  Lung-Chi Chen,et al.  Airway epithelial cells release MIP-3alpha/CCL20 in response to cytokines and ambient particulate matter. , 2003, American journal of respiratory cell and molecular biology.

[25]  M. Jordana,et al.  Intranasal exposure of mice to house dust mite elicits allergic airway inflammation via a GM-CSF-mediated mechanism , 2003 .

[26]  R. Stevens Faculty Opinions recommendation of A protease-activated pathway underlying Th cell type 2 activation and allergic lung disease. , 2002 .

[27]  P. Burgel,et al.  Human Eosinophils Induce Mucin Production in Airway Epithelial Cells Via Epidermal Growth Factor Receptor Activation1 , 2001, The Journal of Immunology.

[28]  C. Soeller,et al.  The transmembrane protein occludin of epithelial tight junctions is a functional target for serine peptidases from faecal pellets of Dermatophagoides pteronyssinus , 2001, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[29]  K. Sekizawa,et al.  Dislocation of E-cadherin in the airway epithelium during an antigen-induced asthmatic response. , 2000, American journal of respiratory cell and molecular biology.

[30]  J. Wegener,et al.  Electric cell-substrate impedance sensing (ECIS) as a noninvasive means to monitor the kinetics of cell spreading to artificial surfaces. , 2000, Experimental cell research.

[31]  P. Thompson,et al.  Der p 1 facilitates transepithelial allergen delivery by disruption of tight junctions. , 1999, The Journal of clinical investigation.

[32]  G. Stewart,et al.  Dust mite proteolytic allergens induce cytokine release from cultured airway epithelium. , 1998, Journal of immunology.

[33]  N. Kalsheker,et al.  On the potential significance of the enzymatic activity of mite allergens to immunogenicity. Clues to structure and function revealed by molecular characterization , 1997, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[34]  S. Holgate The airway epithelium is central to the pathogenesis of asthma. , 2008, Allergology international : official journal of the Japanese Society of Allergology.