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Characterization of immune modulating functions of γδ T cell subsets in a gnotobiotic pig model of human rotavirus infection
Abstract We characterized immune modulating functions of porcine γδ T cell subsets in rotavirus infection using a gnotobiotic pig model of human rotavirus infection and sort-purified lymphocyte autologous co-cultures. We demonstrated that CD2+CD8− and CD2−CD8− γδ T cells have mainly pro-inflammatory...
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Published in: | Comparative immunology, microbiology and infectious diseases microbiology and infectious diseases, 2012-07, Vol.35 (4), p.289-301 |
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description | Abstract We characterized immune modulating functions of porcine γδ T cell subsets in rotavirus infection using a gnotobiotic pig model of human rotavirus infection and sort-purified lymphocyte autologous co-cultures. We demonstrated that CD2+CD8− and CD2−CD8− γδ T cells have mainly pro-inflammatory function as evident by directly secreting IFN-γ or promoting CD4+ αβ T cell proliferation and IFN-γ production, whereas CD2+CD8+ γδ T cells mainly exert regulatory T cell function by expressing FoxP3, secreting IL-10 and TGF-β or increasing IL-10 and TGF-β production by CD4+ αβ T cells. γδ T cells responded to rotavirus infection by increasing TLR2, TLR3, TLR9 expression and IFN-γ and/or TGF-β production. The CD8− subsets likely differentiate into CD8+ subset by acquiring CD8 expression, explaining in part the apparently dual functions of CD2+CD8+ and CD2+CD8− subsets. Thus, both CD8+ and CD8− γδ T cell subsets can contribute to anti-rotavirus immunity and to the maintenance and restoration of intestinal and systemic homeostasis. |
doi_str_mv | 10.1016/j.cimid.2012.01.010 |
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We demonstrated that CD2+CD8− and CD2−CD8− γδ T cells have mainly pro-inflammatory function as evident by directly secreting IFN-γ or promoting CD4+ αβ T cell proliferation and IFN-γ production, whereas CD2+CD8+ γδ T cells mainly exert regulatory T cell function by expressing FoxP3, secreting IL-10 and TGF-β or increasing IL-10 and TGF-β production by CD4+ αβ T cells. γδ T cells responded to rotavirus infection by increasing TLR2, TLR3, TLR9 expression and IFN-γ and/or TGF-β production. The CD8− subsets likely differentiate into CD8+ subset by acquiring CD8 expression, explaining in part the apparently dual functions of CD2+CD8+ and CD2+CD8− subsets. Thus, both CD8+ and CD8− γδ T cell subsets can contribute to anti-rotavirus immunity and to the maintenance and restoration of intestinal and systemic homeostasis.</description><identifier>ISSN: 0147-9571</identifier><identifier>EISSN: 1878-1667</identifier><identifier>DOI: 10.1016/j.cimid.2012.01.010</identifier><identifier>PMID: 22333156</identifier><identifier>CODEN: CIMIDV</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Allergy and Immunology ; Animals ; Biological and medical sciences ; CD2 Antigens - metabolism ; CD4-Positive T-Lymphocytes - immunology ; CD4-Positive T-Lymphocytes - pathology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - pathology ; Coculture Techniques ; Cytokines ; Disease Models, Animal ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; Gammadelta (γδ) T cell subset ; Gene Expression ; Germ-Free Life - immunology ; Gnotobiotic pigs ; Humans ; Infectious Disease ; Interferon-gamma - biosynthesis ; Interferon-gamma - immunology ; Interleukin-10 - biosynthesis ; Interleukin-10 - immunology ; Microbiology ; Miscellaneous ; Receptors, Antigen, T-Cell, gamma-delta - metabolism ; Rotavirus ; Rotavirus Infections - immunology ; Rotavirus Infections - pathology ; Rotavirus Infections - virology ; Swine ; T cell proliferation ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - pathology ; Toll-like receptors ; Toll-Like Receptors - genetics ; Toll-Like Receptors - immunology ; Transforming Growth Factor beta - biosynthesis ; Transforming Growth Factor beta - immunology ; Virology</subject><ispartof>Comparative immunology, microbiology and infectious diseases, 2012-07, Vol.35 (4), p.289-301</ispartof><rights>Elsevier Ltd</rights><rights>2012 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><rights>2012 Elsevier Ltd. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4590-4d709823474ba402fc3efe706ec2ed3bdc292f7daf2f75797ac4e153a705c6223</citedby><cites>FETCH-LOGICAL-c4590-4d709823474ba402fc3efe706ec2ed3bdc292f7daf2f75797ac4e153a705c6223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26037043$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22333156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wen, Ke</creatorcontrib><creatorcontrib>Bui, Tammy</creatorcontrib><creatorcontrib>Li, Guohua</creatorcontrib><creatorcontrib>Liu, Fangning</creatorcontrib><creatorcontrib>Li, Yanru</creatorcontrib><creatorcontrib>Kocher, Jacob</creatorcontrib><creatorcontrib>Yuan, Lijuan</creatorcontrib><title>Characterization of immune modulating functions of γδ T cell subsets in a gnotobiotic pig model of human rotavirus infection</title><title>Comparative immunology, microbiology and infectious diseases</title><addtitle>Comp Immunol Microbiol Infect Dis</addtitle><description>Abstract We characterized immune modulating functions of porcine γδ T cell subsets in rotavirus infection using a gnotobiotic pig model of human rotavirus infection and sort-purified lymphocyte autologous co-cultures. We demonstrated that CD2+CD8− and CD2−CD8− γδ T cells have mainly pro-inflammatory function as evident by directly secreting IFN-γ or promoting CD4+ αβ T cell proliferation and IFN-γ production, whereas CD2+CD8+ γδ T cells mainly exert regulatory T cell function by expressing FoxP3, secreting IL-10 and TGF-β or increasing IL-10 and TGF-β production by CD4+ αβ T cells. γδ T cells responded to rotavirus infection by increasing TLR2, TLR3, TLR9 expression and IFN-γ and/or TGF-β production. The CD8− subsets likely differentiate into CD8+ subset by acquiring CD8 expression, explaining in part the apparently dual functions of CD2+CD8+ and CD2+CD8− subsets. Thus, both CD8+ and CD8− γδ T cell subsets can contribute to anti-rotavirus immunity and to the maintenance and restoration of intestinal and systemic homeostasis.</description><subject>Allergy and Immunology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CD2 Antigens - metabolism</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - pathology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - pathology</subject><subject>Coculture Techniques</subject><subject>Cytokines</subject><subject>Disease Models, Animal</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gammadelta (γδ) T cell subset</subject><subject>Gene Expression</subject><subject>Germ-Free Life - immunology</subject><subject>Gnotobiotic pigs</subject><subject>Humans</subject><subject>Infectious Disease</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interferon-gamma - immunology</subject><subject>Interleukin-10 - biosynthesis</subject><subject>Interleukin-10 - immunology</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Receptors, Antigen, T-Cell, gamma-delta - metabolism</subject><subject>Rotavirus</subject><subject>Rotavirus Infections - immunology</subject><subject>Rotavirus Infections - pathology</subject><subject>Rotavirus Infections - virology</subject><subject>Swine</subject><subject>T cell proliferation</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - pathology</subject><subject>Toll-like receptors</subject><subject>Toll-Like Receptors - genetics</subject><subject>Toll-Like Receptors - immunology</subject><subject>Transforming Growth Factor beta - biosynthesis</subject><subject>Transforming Growth Factor beta - immunology</subject><subject>Virology</subject><issn>0147-9571</issn><issn>1878-1667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkstu1DAUhiMEokPhCZCQN0hsZvAlsZMFlaoRN6kSC8ra8jgnM2dI7MFORioLXqp9jj4Tdmcolw2S5Ug-3__bOf8piueMLhhl8vV2YXHAdsEp4wvK0qIPihmrVT1nUqqHxYyyUs2bSrGT4kmMW0ppw0r2uDjhXAjBKjkrfiw3Jhg7QsDvZkTviO8IDsPkgAy-nfp06Nakm5zN1ZjLt9e3N-SSWOh7EqdVhDESdMSQtfOjX6Ef0ZIdrrMB9FmxmQbjSPCj2WOYMt3Bnd_T4lFn-gjPjt_T4su7t5fLD_OLT-8_Ls8v5rasGjovW0WbmotSlStTUt5ZAR0oKsFyaMWqtbzhnWpNl_ZKNcrYElgljKKVlelvT4uzg-9uWg3QWnBjML3eBRxMuNLeoP674nCj136vhZCSVmUyeHU0CP7bBHHUA8bcAePAT1GnROpa8lplVBxQG3yMAbr7axjNnNRbfZeczslpytKiSfXizxfea35FlYCXR8BEa_ouGGcx_uYkFYqWInFvDhykfu4Rgo4WwVloMaSm69bjfx5y9o_e9ugwXfkVriBu_RRcikozHZNGf85DlmeM8TRfaRc_AYnX0Sw</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Wen, Ke</creator><creator>Bui, Tammy</creator><creator>Li, Guohua</creator><creator>Liu, Fangning</creator><creator>Li, Yanru</creator><creator>Kocher, Jacob</creator><creator>Yuan, Lijuan</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201207</creationdate><title>Characterization of immune modulating functions of γδ T cell subsets in a gnotobiotic pig model of human rotavirus infection</title><author>Wen, Ke ; Bui, Tammy ; Li, Guohua ; Liu, Fangning ; Li, Yanru ; Kocher, Jacob ; Yuan, Lijuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4590-4d709823474ba402fc3efe706ec2ed3bdc292f7daf2f75797ac4e153a705c6223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Allergy and Immunology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CD2 Antigens - metabolism</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD4-Positive T-Lymphocytes - pathology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - pathology</topic><topic>Coculture Techniques</topic><topic>Cytokines</topic><topic>Disease Models, Animal</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gammadelta (γδ) T cell subset</topic><topic>Gene Expression</topic><topic>Germ-Free Life - immunology</topic><topic>Gnotobiotic pigs</topic><topic>Humans</topic><topic>Infectious Disease</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interferon-gamma - immunology</topic><topic>Interleukin-10 - biosynthesis</topic><topic>Interleukin-10 - immunology</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Receptors, Antigen, T-Cell, gamma-delta - metabolism</topic><topic>Rotavirus</topic><topic>Rotavirus Infections - immunology</topic><topic>Rotavirus Infections - pathology</topic><topic>Rotavirus Infections - virology</topic><topic>Swine</topic><topic>T cell proliferation</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocyte Subsets - pathology</topic><topic>Toll-like receptors</topic><topic>Toll-Like Receptors - genetics</topic><topic>Toll-Like Receptors - immunology</topic><topic>Transforming Growth Factor beta - biosynthesis</topic><topic>Transforming Growth Factor beta - immunology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wen, Ke</creatorcontrib><creatorcontrib>Bui, Tammy</creatorcontrib><creatorcontrib>Li, Guohua</creatorcontrib><creatorcontrib>Liu, Fangning</creatorcontrib><creatorcontrib>Li, Yanru</creatorcontrib><creatorcontrib>Kocher, Jacob</creatorcontrib><creatorcontrib>Yuan, Lijuan</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Comparative immunology, microbiology and infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wen, Ke</au><au>Bui, Tammy</au><au>Li, Guohua</au><au>Liu, Fangning</au><au>Li, Yanru</au><au>Kocher, Jacob</au><au>Yuan, Lijuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of immune modulating functions of γδ T cell subsets in a gnotobiotic pig model of human rotavirus infection</atitle><jtitle>Comparative immunology, microbiology and infectious diseases</jtitle><addtitle>Comp Immunol Microbiol Infect Dis</addtitle><date>2012-07</date><risdate>2012</risdate><volume>35</volume><issue>4</issue><spage>289</spage><epage>301</epage><pages>289-301</pages><issn>0147-9571</issn><eissn>1878-1667</eissn><coden>CIMIDV</coden><abstract>Abstract We characterized immune modulating functions of porcine γδ T cell subsets in rotavirus infection using a gnotobiotic pig model of human rotavirus infection and sort-purified lymphocyte autologous co-cultures. We demonstrated that CD2+CD8− and CD2−CD8− γδ T cells have mainly pro-inflammatory function as evident by directly secreting IFN-γ or promoting CD4+ αβ T cell proliferation and IFN-γ production, whereas CD2+CD8+ γδ T cells mainly exert regulatory T cell function by expressing FoxP3, secreting IL-10 and TGF-β or increasing IL-10 and TGF-β production by CD4+ αβ T cells. γδ T cells responded to rotavirus infection by increasing TLR2, TLR3, TLR9 expression and IFN-γ and/or TGF-β production. The CD8− subsets likely differentiate into CD8+ subset by acquiring CD8 expression, explaining in part the apparently dual functions of CD2+CD8+ and CD2+CD8− subsets. Thus, both CD8+ and CD8− γδ T cell subsets can contribute to anti-rotavirus immunity and to the maintenance and restoration of intestinal and systemic homeostasis.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>22333156</pmid><doi>10.1016/j.cimid.2012.01.010</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Allergy and Immunology Animals Biological and medical sciences CD2 Antigens - metabolism CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - pathology CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - pathology Coculture Techniques Cytokines Disease Models, Animal Flow Cytometry Fundamental and applied biological sciences. Psychology Gammadelta (γδ) T cell subset Gene Expression Germ-Free Life - immunology Gnotobiotic pigs Humans Infectious Disease Interferon-gamma - biosynthesis Interferon-gamma - immunology Interleukin-10 - biosynthesis Interleukin-10 - immunology Microbiology Miscellaneous Receptors, Antigen, T-Cell, gamma-delta - metabolism Rotavirus Rotavirus Infections - immunology Rotavirus Infections - pathology Rotavirus Infections - virology Swine T cell proliferation T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - pathology Toll-like receptors Toll-Like Receptors - genetics Toll-Like Receptors - immunology Transforming Growth Factor beta - biosynthesis Transforming Growth Factor beta - immunology Virology |
title | Characterization of immune modulating functions of γδ T cell subsets in a gnotobiotic pig model of human rotavirus infection |
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