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Interleukin-33 amplifies IgE synthesis and triggers mast cell degranulation via interleukin-4 in naïve mice

Background The regulation and function of IgE in healthy individuals and in antigen‐naïve animals is not well understood. IL‐33 administration increases serum IgE in mice with unknown mechanism. We tested the hypothesis that IL‐33 provides an antigen‐independent stimulus for IgE production and mast...

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Published in:Allergy (Copenhagen) 2012-09, Vol.67 (9), p.1118-1126
Main Authors: Komai-Koma, M., Brombacher, F., Pushparaj, P. N., Arendse, B., McSharry, C., Alexander, J., Chaudhuri, R., Thomson, N. C., McKenzie, A. N. J., McInnes, I., Liew, F. Y., Xu, D.
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container_end_page 1126
container_issue 9
container_start_page 1118
container_title Allergy (Copenhagen)
container_volume 67
creator Komai-Koma, M.
Brombacher, F.
Pushparaj, P. N.
Arendse, B.
McSharry, C.
Alexander, J.
Chaudhuri, R.
Thomson, N. C.
McKenzie, A. N. J.
McInnes, I.
Liew, F. Y.
Xu, D.
description Background The regulation and function of IgE in healthy individuals and in antigen‐naïve animals is not well understood. IL‐33 administration increases serum IgE in mice with unknown mechanism. We tested the hypothesis that IL‐33 provides an antigen‐independent stimulus for IgE production and mast cell degranulation. Methods IL‐33 was administered to naïve wild‐type (WT), nude and ST2−/−, IL‐4−/−, IL4Rα−/− and T‐or B‐cell‐specific IL‐4Rα−/− mice. IgEand cytokines were quantified by ELISA. T‐ and B‐lymphocyte numbers and CD40L expression were determined by flow cytometry. Anaphylaxis was measured by temperature, mast cell degranulation and histamine release. Results IL‐33 enhanced IgE production in naïve WT, T‐IL‐4Rα−/− but not in ST2−/−, IL‐4−/−, IL‐4Rα−/− or B‐cell‐specific IL‐4Rα−/− mice, demonstrating IL‐33 specificity and IL‐4 dependency. Moreover, IL‐4 was required for IL‐33‐induced B‐cell proliferation and T‐cell CD40L expression, which promotes IgE production. IL‐33‐induced IL‐4 production was mainly from innate cells including mast cells and eosinophils. IL‐33 increased mast cell surface IgE and triggered degranulation and systemic anaphylaxis in allergen‐naïve WT but not in IL‐4Rα−/− mice. Conclusion IL‐33 amplifies IgE synthesis and triggers anaphylaxis in naïve mice via IL‐4, independent of allergen. IL‐33 may play an important role in nonatopic allergy and idiopathic anaphylaxis.
doi_str_mv 10.1111/j.1398-9995.2012.02859.x
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N. ; Arendse, B. ; McSharry, C. ; Alexander, J. ; Chaudhuri, R. ; Thomson, N. C. ; McKenzie, A. N. J. ; McInnes, I. ; Liew, F. Y. ; Xu, D.</creator><creatorcontrib>Komai-Koma, M. ; Brombacher, F. ; Pushparaj, P. N. ; Arendse, B. ; McSharry, C. ; Alexander, J. ; Chaudhuri, R. ; Thomson, N. C. ; McKenzie, A. N. J. ; McInnes, I. ; Liew, F. Y. ; Xu, D.</creatorcontrib><description>Background The regulation and function of IgE in healthy individuals and in antigen‐naïve animals is not well understood. IL‐33 administration increases serum IgE in mice with unknown mechanism. We tested the hypothesis that IL‐33 provides an antigen‐independent stimulus for IgE production and mast cell degranulation. Methods IL‐33 was administered to naïve wild‐type (WT), nude and ST2−/−, IL‐4−/−, IL4Rα−/− and T‐or B‐cell‐specific IL‐4Rα−/− mice. IgEand cytokines were quantified by ELISA. T‐ and B‐lymphocyte numbers and CD40L expression were determined by flow cytometry. Anaphylaxis was measured by temperature, mast cell degranulation and histamine release. Results IL‐33 enhanced IgE production in naïve WT, T‐IL‐4Rα−/− but not in ST2−/−, IL‐4−/−, IL‐4Rα−/− or B‐cell‐specific IL‐4Rα−/− mice, demonstrating IL‐33 specificity and IL‐4 dependency. Moreover, IL‐4 was required for IL‐33‐induced B‐cell proliferation and T‐cell CD40L expression, which promotes IgE production. IL‐33‐induced IL‐4 production was mainly from innate cells including mast cells and eosinophils. IL‐33 increased mast cell surface IgE and triggered degranulation and systemic anaphylaxis in allergen‐naïve WT but not in IL‐4Rα−/− mice. Conclusion IL‐33 amplifies IgE synthesis and triggers anaphylaxis in naïve mice via IL‐4, independent of allergen. IL‐33 may play an important role in nonatopic allergy and idiopathic anaphylaxis.</description><identifier>ISSN: 0105-4538</identifier><identifier>EISSN: 1398-9995</identifier><identifier>DOI: 10.1111/j.1398-9995.2012.02859.x</identifier><identifier>PMID: 22702477</identifier><identifier>CODEN: LLRGDY</identifier><language>eng</language><publisher>Oxford: Blackwell Publishing Ltd</publisher><subject>allergen independent ; Allergens ; Allergies ; Anaphylaxis ; Anaphylaxis - etiology ; Anaphylaxis - immunology ; Animals ; Biological and medical sciences ; CD40L protein ; Cell Degranulation - immunology ; Cell surface ; Cytokines ; Degranulation ; Dermatology ; Enzyme-linked immunosorbent assay ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Histamine ; Histamine Release ; Hypersensitivity ; IgE ; IL-33 ; IL-4 dependent ; Immunoglobulin E ; Immunoglobulin E - biosynthesis ; Immunoglobulin E - drug effects ; Immunoglobulins ; Interleukin 4 ; Interleukin-33 ; Interleukin-4 - genetics ; Interleukin-4 - immunology ; Interleukin-4 - metabolism ; Interleukins - immunology ; Interleukins - metabolism ; Interleukins - pharmacology ; Leukocytes (eosinophilic) ; Lymphocytes B ; Lymphocytes T ; mast cell degranulation ; Mast cells ; Mast Cells - physiology ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Nude ; Original ; Rodents ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Temperature effects</subject><ispartof>Allergy (Copenhagen), 2012-09, Vol.67 (9), p.1118-1126</ispartof><rights>2012 John Wiley &amp; Sons A/S</rights><rights>2015 INIST-CNRS</rights><rights>2012 John Wiley &amp; Sons A/S.</rights><rights>Copyright © 2012 John Wiley &amp; Sons A/S</rights><rights>Copyright © 2012 John Wiley &amp; Sons A/S 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26290319$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22702477$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Komai-Koma, M.</creatorcontrib><creatorcontrib>Brombacher, F.</creatorcontrib><creatorcontrib>Pushparaj, P. N.</creatorcontrib><creatorcontrib>Arendse, B.</creatorcontrib><creatorcontrib>McSharry, C.</creatorcontrib><creatorcontrib>Alexander, J.</creatorcontrib><creatorcontrib>Chaudhuri, R.</creatorcontrib><creatorcontrib>Thomson, N. C.</creatorcontrib><creatorcontrib>McKenzie, A. N. J.</creatorcontrib><creatorcontrib>McInnes, I.</creatorcontrib><creatorcontrib>Liew, F. Y.</creatorcontrib><creatorcontrib>Xu, D.</creatorcontrib><title>Interleukin-33 amplifies IgE synthesis and triggers mast cell degranulation via interleukin-4 in naïve mice</title><title>Allergy (Copenhagen)</title><addtitle>Allergy</addtitle><description>Background The regulation and function of IgE in healthy individuals and in antigen‐naïve animals is not well understood. IL‐33 administration increases serum IgE in mice with unknown mechanism. We tested the hypothesis that IL‐33 provides an antigen‐independent stimulus for IgE production and mast cell degranulation. Methods IL‐33 was administered to naïve wild‐type (WT), nude and ST2−/−, IL‐4−/−, IL4Rα−/− and T‐or B‐cell‐specific IL‐4Rα−/− mice. IgEand cytokines were quantified by ELISA. T‐ and B‐lymphocyte numbers and CD40L expression were determined by flow cytometry. Anaphylaxis was measured by temperature, mast cell degranulation and histamine release. Results IL‐33 enhanced IgE production in naïve WT, T‐IL‐4Rα−/− but not in ST2−/−, IL‐4−/−, IL‐4Rα−/− or B‐cell‐specific IL‐4Rα−/− mice, demonstrating IL‐33 specificity and IL‐4 dependency. Moreover, IL‐4 was required for IL‐33‐induced B‐cell proliferation and T‐cell CD40L expression, which promotes IgE production. IL‐33‐induced IL‐4 production was mainly from innate cells including mast cells and eosinophils. IL‐33 increased mast cell surface IgE and triggered degranulation and systemic anaphylaxis in allergen‐naïve WT but not in IL‐4Rα−/− mice. Conclusion IL‐33 amplifies IgE synthesis and triggers anaphylaxis in naïve mice via IL‐4, independent of allergen. IL‐33 may play an important role in nonatopic allergy and idiopathic anaphylaxis.</description><subject>allergen independent</subject><subject>Allergens</subject><subject>Allergies</subject><subject>Anaphylaxis</subject><subject>Anaphylaxis - etiology</subject><subject>Anaphylaxis - immunology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CD40L protein</subject><subject>Cell Degranulation - immunology</subject><subject>Cell surface</subject><subject>Cytokines</subject><subject>Degranulation</subject><subject>Dermatology</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Histamine</subject><subject>Histamine Release</subject><subject>Hypersensitivity</subject><subject>IgE</subject><subject>IL-33</subject><subject>IL-4 dependent</subject><subject>Immunoglobulin E</subject><subject>Immunoglobulin E - biosynthesis</subject><subject>Immunoglobulin E - drug effects</subject><subject>Immunoglobulins</subject><subject>Interleukin 4</subject><subject>Interleukin-33</subject><subject>Interleukin-4 - genetics</subject><subject>Interleukin-4 - immunology</subject><subject>Interleukin-4 - metabolism</subject><subject>Interleukins - immunology</subject><subject>Interleukins - metabolism</subject><subject>Interleukins - pharmacology</subject><subject>Leukocytes (eosinophilic)</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>mast cell degranulation</subject><subject>Mast cells</subject><subject>Mast Cells - physiology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Nude</subject><subject>Original</subject><subject>Rodents</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Temperature effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Komai-Koma, M.</creatorcontrib><creatorcontrib>Brombacher, F.</creatorcontrib><creatorcontrib>Pushparaj, P. N.</creatorcontrib><creatorcontrib>Arendse, B.</creatorcontrib><creatorcontrib>McSharry, C.</creatorcontrib><creatorcontrib>Alexander, J.</creatorcontrib><creatorcontrib>Chaudhuri, R.</creatorcontrib><creatorcontrib>Thomson, N. C.</creatorcontrib><creatorcontrib>McKenzie, A. N. J.</creatorcontrib><creatorcontrib>McInnes, I.</creatorcontrib><creatorcontrib>Liew, F. Y.</creatorcontrib><creatorcontrib>Xu, D.</creatorcontrib><collection>Istex</collection><collection>Wiley_OA刊</collection><collection>Wiley Online Library Journals</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Allergy (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Komai-Koma, M.</au><au>Brombacher, F.</au><au>Pushparaj, P. N.</au><au>Arendse, B.</au><au>McSharry, C.</au><au>Alexander, J.</au><au>Chaudhuri, R.</au><au>Thomson, N. C.</au><au>McKenzie, A. N. J.</au><au>McInnes, I.</au><au>Liew, F. Y.</au><au>Xu, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-33 amplifies IgE synthesis and triggers mast cell degranulation via interleukin-4 in naïve mice</atitle><jtitle>Allergy (Copenhagen)</jtitle><addtitle>Allergy</addtitle><date>2012-09</date><risdate>2012</risdate><volume>67</volume><issue>9</issue><spage>1118</spage><epage>1126</epage><pages>1118-1126</pages><issn>0105-4538</issn><eissn>1398-9995</eissn><coden>LLRGDY</coden><abstract>Background The regulation and function of IgE in healthy individuals and in antigen‐naïve animals is not well understood. IL‐33 administration increases serum IgE in mice with unknown mechanism. We tested the hypothesis that IL‐33 provides an antigen‐independent stimulus for IgE production and mast cell degranulation. Methods IL‐33 was administered to naïve wild‐type (WT), nude and ST2−/−, IL‐4−/−, IL4Rα−/− and T‐or B‐cell‐specific IL‐4Rα−/− mice. IgEand cytokines were quantified by ELISA. T‐ and B‐lymphocyte numbers and CD40L expression were determined by flow cytometry. Anaphylaxis was measured by temperature, mast cell degranulation and histamine release. Results IL‐33 enhanced IgE production in naïve WT, T‐IL‐4Rα−/− but not in ST2−/−, IL‐4−/−, IL‐4Rα−/− or B‐cell‐specific IL‐4Rα−/− mice, demonstrating IL‐33 specificity and IL‐4 dependency. Moreover, IL‐4 was required for IL‐33‐induced B‐cell proliferation and T‐cell CD40L expression, which promotes IgE production. IL‐33‐induced IL‐4 production was mainly from innate cells including mast cells and eosinophils. IL‐33 increased mast cell surface IgE and triggered degranulation and systemic anaphylaxis in allergen‐naïve WT but not in IL‐4Rα−/− mice. Conclusion IL‐33 amplifies IgE synthesis and triggers anaphylaxis in naïve mice via IL‐4, independent of allergen. IL‐33 may play an important role in nonatopic allergy and idiopathic anaphylaxis.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>22702477</pmid><doi>10.1111/j.1398-9995.2012.02859.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0105-4538
ispartof Allergy (Copenhagen), 2012-09, Vol.67 (9), p.1118-1126
issn 0105-4538
1398-9995
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3660789
source Wiley-Blackwell Read & Publish Collection
subjects allergen independent
Allergens
Allergies
Anaphylaxis
Anaphylaxis - etiology
Anaphylaxis - immunology
Animals
Biological and medical sciences
CD40L protein
Cell Degranulation - immunology
Cell surface
Cytokines
Degranulation
Dermatology
Enzyme-linked immunosorbent assay
Flow Cytometry
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Histamine
Histamine Release
Hypersensitivity
IgE
IL-33
IL-4 dependent
Immunoglobulin E
Immunoglobulin E - biosynthesis
Immunoglobulin E - drug effects
Immunoglobulins
Interleukin 4
Interleukin-33
Interleukin-4 - genetics
Interleukin-4 - immunology
Interleukin-4 - metabolism
Interleukins - immunology
Interleukins - metabolism
Interleukins - pharmacology
Leukocytes (eosinophilic)
Lymphocytes B
Lymphocytes T
mast cell degranulation
Mast cells
Mast Cells - physiology
Medical sciences
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Nude
Original
Rodents
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Temperature effects
title Interleukin-33 amplifies IgE synthesis and triggers mast cell degranulation via interleukin-4 in naïve mice
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