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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 |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3660789</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1038606053</sourcerecordid><originalsourceid>FETCH-LOGICAL-i5659-72dcfed71a1965a93a3501d10b413b8e354865eeef802374a9e550909d9007353</originalsourceid><addsrcrecordid>eNqNksFu1DAQhiMEokvhFZAlhMQlwY5jOz6AVJW2LIoKlUAcLW8ySb11nG2cLLtP1YfgxXC6y1I44YttzTe_Zzx_FCGCExLW22VCqMxjKSVLUkzSBKc5k8nmUTQ7BB5HM0wwizNG86PomfdLjLFIJX4aHaWpwGkmxCyyczdAb2G8MS6mFOl2ZU1twKN5c4b81g3X4I1H2lVo6E3TQO9Rq_2ASrAWVdD02o1WD6ZzaG00Mg_0snBDTv-8WwNqTQnPoye1th5e7Pfj6Nv52dfTj3Hx-WJ-elLEhnEmY5FWZQ2VIJpIzrSkmjJMKoIXGaGLHCjLcs4AoM5xSkWmJTCGJZaVDB1SRo-j9zvd1bhooSrBDb22atWbVvdb1Wmj_o44c62abq0o51jkMgi82Qv03e0IflCt8VPD2kE3ekUwzTnmmNH_QWnGSC54QF_9gy67sXfhJ-6pUHvGp7dfPiz-UPXvmQXg9R7QvtS2DgMojf_D8TBjSiahdzvuh7GwPcQJVpOH1FJNVlGTVdTkIXXvIbVRJ0UxnUJ-vMs3foDNIV_3N4oLKpj6fnmh0g-Xn74UV1eK0l9B-cj0</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1033007469</pqid></control><display><type>article</type><title>Interleukin-33 amplifies IgE synthesis and triggers mast cell degranulation via interleukin-4 in naïve mice</title><source>Wiley-Blackwell Read & Publish Collection</source><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.</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 & Sons A/S</rights><rights>2015 INIST-CNRS</rights><rights>2012 John Wiley & Sons A/S.</rights><rights>Copyright © 2012 John Wiley & Sons A/S</rights><rights>Copyright © 2012 John Wiley & 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&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. Vasculitis</subject><subject>Temperature effects</subject><issn>0105-4538</issn><issn>1398-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqNksFu1DAQhiMEokvhFZAlhMQlwY5jOz6AVJW2LIoKlUAcLW8ySb11nG2cLLtP1YfgxXC6y1I44YttzTe_Zzx_FCGCExLW22VCqMxjKSVLUkzSBKc5k8nmUTQ7BB5HM0wwizNG86PomfdLjLFIJX4aHaWpwGkmxCyyczdAb2G8MS6mFOl2ZU1twKN5c4b81g3X4I1H2lVo6E3TQO9Rq_2ASrAWVdD02o1WD6ZzaG00Mg_0snBDTv-8WwNqTQnPoye1th5e7Pfj6Nv52dfTj3Hx-WJ-elLEhnEmY5FWZQ2VIJpIzrSkmjJMKoIXGaGLHCjLcs4AoM5xSkWmJTCGJZaVDB1SRo-j9zvd1bhooSrBDb22atWbVvdb1Wmj_o44c62abq0o51jkMgi82Qv03e0IflCt8VPD2kE3ekUwzTnmmNH_QWnGSC54QF_9gy67sXfhJ-6pUHvGp7dfPiz-UPXvmQXg9R7QvtS2DgMojf_D8TBjSiahdzvuh7GwPcQJVpOH1FJNVlGTVdTkIXXvIbVRJ0UxnUJ-vMs3foDNIV_3N4oLKpj6fnmh0g-Xn74UV1eK0l9B-cj0</recordid><startdate>201209</startdate><enddate>201209</enddate><creator>Komai-Koma, M.</creator><creator>Brombacher, F.</creator><creator>Pushparaj, P. N.</creator><creator>Arendse, B.</creator><creator>McSharry, C.</creator><creator>Alexander, J.</creator><creator>Chaudhuri, R.</creator><creator>Thomson, N. C.</creator><creator>McKenzie, A. N. J.</creator><creator>McInnes, I.</creator><creator>Liew, F. Y.</creator><creator>Xu, D.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>24P</scope><scope>WIN</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201209</creationdate><title>Interleukin-33 amplifies IgE synthesis and triggers mast cell degranulation via interleukin-4 in naïve mice</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i5659-72dcfed71a1965a93a3501d10b413b8e354865eeef802374a9e550909d9007353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>allergen independent</topic><topic>Allergens</topic><topic>Allergies</topic><topic>Anaphylaxis</topic><topic>Anaphylaxis - etiology</topic><topic>Anaphylaxis - immunology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CD40L protein</topic><topic>Cell Degranulation - immunology</topic><topic>Cell surface</topic><topic>Cytokines</topic><topic>Degranulation</topic><topic>Dermatology</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Histamine</topic><topic>Histamine Release</topic><topic>Hypersensitivity</topic><topic>IgE</topic><topic>IL-33</topic><topic>IL-4 dependent</topic><topic>Immunoglobulin E</topic><topic>Immunoglobulin E - biosynthesis</topic><topic>Immunoglobulin E - drug effects</topic><topic>Immunoglobulins</topic><topic>Interleukin 4</topic><topic>Interleukin-33</topic><topic>Interleukin-4 - genetics</topic><topic>Interleukin-4 - immunology</topic><topic>Interleukin-4 - metabolism</topic><topic>Interleukins - immunology</topic><topic>Interleukins - metabolism</topic><topic>Interleukins - pharmacology</topic><topic>Leukocytes (eosinophilic)</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>mast cell degranulation</topic><topic>Mast cells</topic><topic>Mast Cells - physiology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Nude</topic><topic>Original</topic><topic>Rodents</topic><topic>Sarcoidosis. 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 & 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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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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