The CD28-Related Molecule ICOS Is Required for Effective T Cell–Dependent Immune Responses
While CD28 is critical for expansion of naive T cells, recent evidence suggests that the activation of effector T cells is largely independent of CD28/B7. We suggest that ICOS, the third member of the CD28/CTLA-4 family, plays an important role in production of IL-2, IL-4, IL-5, and IFNγ from recent...
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Veröffentlicht in: | Immunity (Cambridge, Mass.) Mass.), 2000-07, Vol.13 (1), p.95-105 |
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creator | Coyle, Anthony J Lehar, Sophie Lloyd, Clare Tian, Jane Delaney, Tracy Manning, Stephen Nguyen, Trang Burwell, Tim Schneider, Helga Gonzalo, Jose Angel Gosselin, Michael Owen, Laura Rudolph Rudd, Christopher E Gutierrez-Ramos, Jose Carlos |
description | While CD28 is critical for expansion of naive T cells, recent evidence suggests that the activation of effector T cells is largely independent of CD28/B7. We suggest that ICOS, the third member of the CD28/CTLA-4 family, plays an important role in production of IL-2, IL-4, IL-5, and IFNγ from recently activated T cells and contributes to T cell–dependent B help in vivo. Inhibition of ICOS attenuates lung mucosal inflammation induced by Th2 but not Th1 effector populations. Our data indicate a critical function for the third member of the CD28 family in T cell–dependent immune responses. |
doi_str_mv | 10.1016/S1074-7613(00)00011-X |
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We suggest that ICOS, the third member of the CD28/CTLA-4 family, plays an important role in production of IL-2, IL-4, IL-5, and IFNγ from recently activated T cells and contributes to T cell–dependent B help in vivo. Inhibition of ICOS attenuates lung mucosal inflammation induced by Th2 but not Th1 effector populations. Our data indicate a critical function for the third member of the CD28 family in T cell–dependent immune responses.</description><subject>Abatacept</subject><subject>AIDS/HIV</subject><subject>Animals</subject><subject>Antigens, CD</subject><subject>Antigens, Differentiation - immunology</subject><subject>Antigens, Differentiation, T-Lymphocyte - genetics</subject><subject>Antigens, Differentiation, T-Lymphocyte - immunology</subject><subject>CD28 antigen</subject><subject>CD28 Antigens - immunology</subject><subject>Cloning, Molecular</subject><subject>CTLA-4 Antigen</subject><subject>Cytokines - biosynthesis</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>ICOS protein</subject><subject>Immunoconjugates</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin M - biosynthesis</subject><subject>Inducible T-Cell Co-Stimulator Protein</subject><subject>Jurkat Cells</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Transgenic</subject><subject>Signal Transduction</subject><subject>Th1 Cells - immunology</subject><subject>Th2 Cells - immunology</subject><issn>1074-7613</issn><issn>1097-4180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1Kw0AQxxdRrF-PoOxJ9BCdSTZfJ5FYtaAUtEIPwrLZTDCSj5pNBG--g2_ok7hpe_DWy8zA_v4zy4-xY4QLBAwunxFC4YQBemcA5wCA6My32B5CHDoCI9ge5jUyYvvGvFtG-DHsspGFPM-Loz32Onsjnty4kfNEpeoo449NSboviU-S6TOfGP5EH33R2pe8afk4z0l3xSfxGU-oLH-_f25oQXVGdccnVdXXZANm0dSGzCHbyVVp6GjdD9jL7XiW3DsP07tJcv3gaBFj5wQhZV6AaaQViMBXrvZ9cIEgFVqQQI0CVKqi2MuG4it0U4F2TAOVpTryDtjpau-ibT56Mp2sCqPt71RNTW9kiG7oWSUbQQwDF9AdNvorULeNMS3lctEWlWq_JIIc_MulfznIlQBy6V_Obe5kfaBPK8r-pVbCLXC1Asj6-CyolUYXVGvKrGLdyawpNpz4A22BlBI</recordid><startdate>20000701</startdate><enddate>20000701</enddate><creator>Coyle, Anthony J</creator><creator>Lehar, Sophie</creator><creator>Lloyd, Clare</creator><creator>Tian, Jane</creator><creator>Delaney, Tracy</creator><creator>Manning, Stephen</creator><creator>Nguyen, Trang</creator><creator>Burwell, Tim</creator><creator>Schneider, Helga</creator><creator>Gonzalo, Jose Angel</creator><creator>Gosselin, Michael</creator><creator>Owen, Laura Rudolph</creator><creator>Rudd, Christopher E</creator><creator>Gutierrez-Ramos, Jose Carlos</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20000701</creationdate><title>The CD28-Related Molecule ICOS Is Required for Effective T Cell–Dependent Immune Responses</title><author>Coyle, Anthony J ; 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We suggest that ICOS, the third member of the CD28/CTLA-4 family, plays an important role in production of IL-2, IL-4, IL-5, and IFNγ from recently activated T cells and contributes to T cell–dependent B help in vivo. Inhibition of ICOS attenuates lung mucosal inflammation induced by Th2 but not Th1 effector populations. Our data indicate a critical function for the third member of the CD28 family in T cell–dependent immune responses.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10933398</pmid><doi>10.1016/S1074-7613(00)00011-X</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abatacept AIDS/HIV Animals Antigens, CD Antigens, Differentiation - immunology Antigens, Differentiation, T-Lymphocyte - genetics Antigens, Differentiation, T-Lymphocyte - immunology CD28 antigen CD28 Antigens - immunology Cloning, Molecular CTLA-4 Antigen Cytokines - biosynthesis Gene Expression Humans ICOS protein Immunoconjugates Immunoglobulin G - biosynthesis Immunoglobulin M - biosynthesis Inducible T-Cell Co-Stimulator Protein Jurkat Cells Male Mice Mice, Inbred BALB C Mice, Transgenic Signal Transduction Th1 Cells - immunology Th2 Cells - immunology |
title | The CD28-Related Molecule ICOS Is Required for Effective T Cell–Dependent Immune Responses |
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