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dc.contributor.author Hristova M
dc.contributor.author Habibovic A
dc.contributor.author Veith C
dc.contributor.author Janssen-Heininger YMW
dc.contributor.author Dixon AE
dc.contributor.author Geiszt, Miklós
dc.contributor.author van der Vliet A
dc.date.accessioned 2018-07-13T08:09:21Z
dc.date.available 2018-07-13T08:09:21Z
dc.date.issued 2016
dc.identifier 84948845194
dc.identifier.citation pagination=1545-1556e11; journalVolume=137; journalIssueNumber=5; journalTitle=JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4807
dc.identifier.uri doi:10.1016/j.jaci.2015.10.003
dc.description.abstract Background: The IL-1 family member IL-33 plays a critical role in type 2 innate immune responses to allergens and is an important mediator of allergic asthma. The mechanisms by which allergens provoke epithelial IL-33 secretion are still poorly understood. Objective: Based on previous findings indicating involvement of the NADPH oxidase dual oxidase 1 (DUOX1) in epithelial wound responses, we explored the potential involvement of DUOX1 in allergen-induced IL-33 secretion and potential alterations in airways of asthmatic patients. Methods: Cultured human or murine airway epithelial cells or mice were subjected to acute challenge with Alternaria alternata or house dust mite, and secretion of IL-33 and activation of subsequent type 2 responses were determined. The role of DUOX1 was explored by using small interfering RNA approaches and DUOX1-deficient mice. Cultured nasal epithelial cells from healthy subjects or asthmatic patients were evaluated for DUOX1 expression and allergen-induced responses. Results: In vitro or in vivo allergen challenge resulted in rapid airway epithelial IL-33 secretion, which depended critically on DUOX1-mediated activation of epithelial epidermal growth factor receptor and the protease calpain-2 through a redox-dependent mechanism involving cysteine oxidation within epidermal growth factor receptor and the tyrosine kinase Src. Primary nasal epithelial cells from patients with allergic asthma were found to express increased DUOX1 and IL-33 levels and demonstrated enhanced IL-33 secretion in response to allergen challenge compared with values seen in nasal epithelial cells from nonasthmatic subjects. Conclusion: Our findings implicate epithelial DUOX1 as a pivotal mediator of IL-33-dependent activation of innate airway type 2 immune responses to common airborne allergens and indicate that enhanced DUOX1 expression and IL-33 secretion might present important contributing features of allergic asthma. © 2015 American Academy of Allergy, Asthma & Immunology.
dc.relation.ispartof urn:issn:0091-6749
dc.title Airway epithelial dual oxidase 1 mediates allergen-induced IL-33 secretion and activation of type 2 immune responses
dc.type Journal Article
dc.date.updated 2018-02-16T09:59:54Z
dc.language.rfc3066 en
dc.identifier.mtmt 2993720
dc.identifier.wos 000376180200031
dc.contributor.department SE/AOK/I/ÉI/MTA-SE Lendület Peroxidáz Enzimek Kutatócsoport [2016.12.31]
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote FELTÖLTŐ: Sonnevend Kinga - sonnevend.kinga@med.semmelweis-univ.hu


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