The T cell activation molecule H4 and the CD28‐like molecule ICOS are identical

The recently cloned CD28‐like molecule ICOS displays striking similarities with H4, characterized some years ago in the mouse and recently in humans. Both molecules are selectively expressed by activated and germinal center T cells, display similar structure, and display co‐stimulatory activities. H...

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Veröffentlicht in:European journal of immunology 2000-12, Vol.30 (12), p.3463-3467
Hauptverfasser: Buonfiglio, Donatella, Bragardo, Manuela, Redoglia, Valter, Vaschetto, Rosanna, Bottarel, Flavia, Bonissoni, Sara, Bensi, Thea, Mezzatesta, Caterina, Janeway jr, Charles A., Dianzani, Umberto
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container_end_page 3467
container_issue 12
container_start_page 3463
container_title European journal of immunology
container_volume 30
creator Buonfiglio, Donatella
Bragardo, Manuela
Redoglia, Valter
Vaschetto, Rosanna
Bottarel, Flavia
Bonissoni, Sara
Bensi, Thea
Mezzatesta, Caterina
Janeway jr, Charles A.
Dianzani, Umberto
description The recently cloned CD28‐like molecule ICOS displays striking similarities with H4, characterized some years ago in the mouse and recently in humans. Both molecules are selectively expressed by activated and germinal center T cells, display similar structure, and display co‐stimulatory activities. H4 displays lateral association with the CD3/TCR and is expressed by mature thymocytes. In the mouse, H4 is also expressed at high levels by thymic NKT cells that are resistant to negative selection. The aim of this work was to evaluate whether H4 and ICOS are the same molecule using the C398.4A (binding human and mouse H4) and F44 (binding human ICOS) monoclonal antibody (mAb) in parallel experiments on human T cells. ICOS and H4 displayed the same expression pattern in a panel of T cell lines and the same expression kinetics in phytohemagglutinin‐activated T cells. C398.4A completely blocked cell staining by F44, whereas F44 partially blocked C398.4A. H4 and ICOS immunoprecipitates displayed identical SDS‐PAGE patterns and H4 immunoprecipitation completely removed ICOS from cell lysates. Finally, the C398.4A mAb specifically stained cells transfected with the human or mouse ICOS. These data prove that H4 and ICOS are the same molecule and that F44 and C398.4A bind partially different epitopes.
doi_str_mv 10.1002/1521-4141(2000012)30:12<3463::AID-IMMU3463>3.0.CO;2-5
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Both molecules are selectively expressed by activated and germinal center T cells, display similar structure, and display co‐stimulatory activities. H4 displays lateral association with the CD3/TCR and is expressed by mature thymocytes. In the mouse, H4 is also expressed at high levels by thymic NKT cells that are resistant to negative selection. The aim of this work was to evaluate whether H4 and ICOS are the same molecule using the C398.4A (binding human and mouse H4) and F44 (binding human ICOS) monoclonal antibody (mAb) in parallel experiments on human T cells. ICOS and H4 displayed the same expression pattern in a panel of T cell lines and the same expression kinetics in phytohemagglutinin‐activated T cells. C398.4A completely blocked cell staining by F44, whereas F44 partially blocked C398.4A. H4 and ICOS immunoprecipitates displayed identical SDS‐PAGE patterns and H4 immunoprecipitation completely removed ICOS from cell lysates. Finally, the C398.4A mAb specifically stained cells transfected with the human or mouse ICOS. 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Both molecules are selectively expressed by activated and germinal center T cells, display similar structure, and display co‐stimulatory activities. H4 displays lateral association with the CD3/TCR and is expressed by mature thymocytes. In the mouse, H4 is also expressed at high levels by thymic NKT cells that are resistant to negative selection. The aim of this work was to evaluate whether H4 and ICOS are the same molecule using the C398.4A (binding human and mouse H4) and F44 (binding human ICOS) monoclonal antibody (mAb) in parallel experiments on human T cells. ICOS and H4 displayed the same expression pattern in a panel of T cell lines and the same expression kinetics in phytohemagglutinin‐activated T cells. C398.4A completely blocked cell staining by F44, whereas F44 partially blocked C398.4A. H4 and ICOS immunoprecipitates displayed identical SDS‐PAGE patterns and H4 immunoprecipitation completely removed ICOS from cell lysates. Finally, the C398.4A mAb specifically stained cells transfected with the human or mouse ICOS. These data prove that H4 and ICOS are the same molecule and that F44 and C398.4A bind partially different epitopes.</description><subject>Animals</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antigens, Differentiation, T-Lymphocyte - analysis</subject><subject>Antigens, Differentiation, T-Lymphocyte - physiology</subject><subject>CD28</subject><subject>CD28 antigen</subject><subject>Cell Line</subject><subject>CTLA‐4</subject><subject>Humans</subject><subject>ICOS</subject><subject>ICOS protein</subject><subject>Immunodominant Epitopes - analysis</subject><subject>Immunodominant Epitopes - physiology</subject><subject>Inducible T-Cell Co-Stimulator Protein</subject><subject>Mice</subject><subject>Precipitin Tests</subject><subject>Protozoan Proteins</subject><subject>T cell co‐stimulation</subject><subject>T-Lymphocytes - chemistry</subject><issn>0014-2980</issn><issn>1521-4141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUU1PGzEQtaqiEkL_QuVTVQ4bPLbXWacFCS1fkUARIlx6GXmdWXXbTZbubkDc-An8Rn4JXiWEU1Xhg63xvHnzZh5jByAGIITch1hCpEHDNynCAbmnxAjkD6WNGo2OxsfR-PLyposO1UAM0sl3GcUfWG9T95H1QpmOpE3ENttpmt-BxprYfmLbAMIqMHGPXU1_EZ9yT2XJnW-LO9cW1YLPq5L8siR-rrlbzHgbUOmxTJ4fn8riD73lx-nkmruaeDGjRVt4V-6yrdyVDX1ev312c3oyTc-ji8nZOD26iLyyVkUZSMhs7LQmb6x0WS4EKQvKg9M2k7nWzrtEakcm8VpbGSvKw3R5YoXSmeqzryve27r6u6SmxXnRdHO4BVXLBocgh1qK-L9AGA6NNcaojVJfV01TU463dTF39QOCwM4U7JaL3XJxbQqqkAl3sAExmIKvpqBCgekEJXYCvqwFLLM5zd5Y1y4EwM8V4L4o6eF9Xf_RdPOnXgBsrqRg</recordid><startdate>200012</startdate><enddate>200012</enddate><creator>Buonfiglio, Donatella</creator><creator>Bragardo, Manuela</creator><creator>Redoglia, Valter</creator><creator>Vaschetto, Rosanna</creator><creator>Bottarel, Flavia</creator><creator>Bonissoni, Sara</creator><creator>Bensi, Thea</creator><creator>Mezzatesta, Caterina</creator><creator>Janeway jr, Charles A.</creator><creator>Dianzani, Umberto</creator><general>WILEY‐VCH Verlag GmbH</general><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>200012</creationdate><title>The T cell activation molecule H4 and the CD28‐like molecule ICOS are identical</title><author>Buonfiglio, Donatella ; Bragardo, Manuela ; Redoglia, Valter ; Vaschetto, Rosanna ; Bottarel, Flavia ; Bonissoni, Sara ; Bensi, Thea ; Mezzatesta, Caterina ; Janeway jr, Charles A. ; Dianzani, Umberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3993-b121b95a44ec692abf00e3913c1a49b2f44aca824ae68c449253ef152f89034b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antigens, Differentiation, T-Lymphocyte - analysis</topic><topic>Antigens, Differentiation, T-Lymphocyte - physiology</topic><topic>CD28</topic><topic>CD28 antigen</topic><topic>Cell Line</topic><topic>CTLA‐4</topic><topic>Humans</topic><topic>ICOS</topic><topic>ICOS protein</topic><topic>Immunodominant Epitopes - analysis</topic><topic>Immunodominant Epitopes - physiology</topic><topic>Inducible T-Cell Co-Stimulator Protein</topic><topic>Mice</topic><topic>Precipitin Tests</topic><topic>Protozoan Proteins</topic><topic>T cell co‐stimulation</topic><topic>T-Lymphocytes - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buonfiglio, Donatella</creatorcontrib><creatorcontrib>Bragardo, Manuela</creatorcontrib><creatorcontrib>Redoglia, Valter</creatorcontrib><creatorcontrib>Vaschetto, Rosanna</creatorcontrib><creatorcontrib>Bottarel, Flavia</creatorcontrib><creatorcontrib>Bonissoni, Sara</creatorcontrib><creatorcontrib>Bensi, Thea</creatorcontrib><creatorcontrib>Mezzatesta, Caterina</creatorcontrib><creatorcontrib>Janeway jr, Charles A.</creatorcontrib><creatorcontrib>Dianzani, Umberto</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buonfiglio, Donatella</au><au>Bragardo, Manuela</au><au>Redoglia, Valter</au><au>Vaschetto, Rosanna</au><au>Bottarel, Flavia</au><au>Bonissoni, Sara</au><au>Bensi, Thea</au><au>Mezzatesta, Caterina</au><au>Janeway jr, Charles A.</au><au>Dianzani, Umberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The T cell activation molecule H4 and the CD28‐like molecule ICOS are identical</atitle><jtitle>European journal of immunology</jtitle><addtitle>Eur J Immunol</addtitle><date>2000-12</date><risdate>2000</risdate><volume>30</volume><issue>12</issue><spage>3463</spage><epage>3467</epage><pages>3463-3467</pages><issn>0014-2980</issn><eissn>1521-4141</eissn><abstract>The recently cloned CD28‐like molecule ICOS displays striking similarities with H4, characterized some years ago in the mouse and recently in humans. Both molecules are selectively expressed by activated and germinal center T cells, display similar structure, and display co‐stimulatory activities. H4 displays lateral association with the CD3/TCR and is expressed by mature thymocytes. In the mouse, H4 is also expressed at high levels by thymic NKT cells that are resistant to negative selection. The aim of this work was to evaluate whether H4 and ICOS are the same molecule using the C398.4A (binding human and mouse H4) and F44 (binding human ICOS) monoclonal antibody (mAb) in parallel experiments on human T cells. ICOS and H4 displayed the same expression pattern in a panel of T cell lines and the same expression kinetics in phytohemagglutinin‐activated T cells. C398.4A completely blocked cell staining by F44, whereas F44 partially blocked C398.4A. H4 and ICOS immunoprecipitates displayed identical SDS‐PAGE patterns and H4 immunoprecipitation completely removed ICOS from cell lysates. Finally, the C398.4A mAb specifically stained cells transfected with the human or mouse ICOS. These data prove that H4 and ICOS are the same molecule and that F44 and C398.4A bind partially different epitopes.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><pmid>11093165</pmid><doi>10.1002/1521-4141(2000012)30:12&lt;3463::AID-IMMU3463&gt;3.0.CO;2-5</doi><tpages>5</tpages></addata></record>
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source Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals
subjects Animals
Antibodies, Monoclonal - immunology
Antigens, Differentiation, T-Lymphocyte - analysis
Antigens, Differentiation, T-Lymphocyte - physiology
CD28
CD28 antigen
Cell Line
CTLA‐4
Humans
ICOS
ICOS protein
Immunodominant Epitopes - analysis
Immunodominant Epitopes - physiology
Inducible T-Cell Co-Stimulator Protein
Mice
Precipitin Tests
Protozoan Proteins
T cell co‐stimulation
T-Lymphocytes - chemistry
title The T cell activation molecule H4 and the CD28‐like molecule ICOS are identical
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