Two types of mouse helper T cell clone. III: Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies
Lymphokine synthesis patterns of a panel of 19 T cell clones have been evaluated, using mRNA hybridization methods to examine 11 different mRNAs induced by Con A. The two types of CD4+ Th cell clone described previously were clearly distinguished by this procedure, and the differences between the tw...
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Veröffentlicht in: | The Journal of experimental medicine 1987-11, Vol.166 (5), p.1229-1244 |
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description | Lymphokine synthesis patterns of a panel of 19 T cell clones have been evaluated, using mRNA hybridization methods to examine 11 different mRNAs induced by Con A. The two types of CD4+ Th cell clone described previously were clearly distinguished by this procedure, and the differences between the two types have now been extended to six induced products. With minor exceptions, only Th1 clones synthesized mRNA for IL-2, IFN-gamma, and lymphotoxin, and only Th2 clones synthesized mRNA for IL-4, IL-5, and another induced gene, P600. Four more induced products were expressed preferentially but not uniquely by one or another type of clone: mRNAs for GM-CSF, TNF, and another induced, secreted product (TY5) were produced in larger amounts by Th1 clones, whereas preproenkephalin was preferentially expressed by Th2 clones. IL-3 was produced in similar amounts by both types of clone. mAbs were used to establish three bioassays that were functionally monospecific for IL-2, IL-3, and IL-4, and a new anti-IFN gamma mAb, XMG1.2, was used to establish an ELISA for IFN-gamma. These four assays were used to show that secreted protein and mRNA levels correlated well for all cell lines. The implications of these findings for normal T cells are discussed. |
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III: Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>CHERWINSKI, H. M ; SCHUMACHER, J. H ; BROWN, K. D ; MOSMANN, T. R</creator><creatorcontrib>CHERWINSKI, H. M ; SCHUMACHER, J. H ; BROWN, K. D ; MOSMANN, T. R</creatorcontrib><description>Lymphokine synthesis patterns of a panel of 19 T cell clones have been evaluated, using mRNA hybridization methods to examine 11 different mRNAs induced by Con A. The two types of CD4+ Th cell clone described previously were clearly distinguished by this procedure, and the differences between the two types have now been extended to six induced products. With minor exceptions, only Th1 clones synthesized mRNA for IL-2, IFN-gamma, and lymphotoxin, and only Th2 clones synthesized mRNA for IL-4, IL-5, and another induced gene, P600. Four more induced products were expressed preferentially but not uniquely by one or another type of clone: mRNAs for GM-CSF, TNF, and another induced, secreted product (TY5) were produced in larger amounts by Th1 clones, whereas preproenkephalin was preferentially expressed by Th2 clones. IL-3 was produced in similar amounts by both types of clone. mAbs were used to establish three bioassays that were functionally monospecific for IL-2, IL-3, and IL-4, and a new anti-IFN gamma mAb, XMG1.2, was used to establish an ELISA for IFN-gamma. These four assays were used to show that secreted protein and mRNA levels correlated well for all cell lines. The implications of these findings for normal T cells are discussed.</description><identifier>ISSN: 0022-1007</identifier><identifier>EISSN: 1540-9538</identifier><identifier>DOI: 10.1084/jem.166.5.1229</identifier><identifier>PMID: 2960769</identifier><identifier>CODEN: JEMEAV</identifier><language>eng</language><publisher>New York, NY: Rockefeller University Press</publisher><subject>Analysis of the immune response. Humoral and cellular immunity ; Animals ; Antibodies, Monoclonal ; Applied sciences ; Biological and medical sciences ; Biological Assay ; Cell Division ; Cell Line ; Clone Cells - metabolism ; Colony-Stimulating Factors - biosynthesis ; Enkephalins - biosynthesis ; Exact sciences and technology ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Granulocyte-Macrophage Colony-Stimulating Factor ; Growth Substances - biosynthesis ; Immunobiology ; Interferon-gamma - biosynthesis ; Interleukin-2 - biosynthesis ; Interleukin-3 - biosynthesis ; Interleukin-4 ; Interleukin-5 ; Interleukins - biosynthesis ; Lymphokines - biosynthesis ; Lymphokines - genetics ; Lymphokines - pharmacology ; Lymphotoxin-alpha - biosynthesis ; Mice ; Mice, Inbred Strains ; Nucleic Acid Hybridization ; Organs and cells involved in the immune response ; Other techniques and industries ; Protein Precursors - biosynthesis ; RNA, Messenger - genetics ; T-Lymphocytes, Helper-Inducer - metabolism ; Tumor Necrosis Factor-alpha - biosynthesis</subject><ispartof>The Journal of experimental medicine, 1987-11, Vol.166 (5), p.1229-1244</ispartof><rights>1989 INIST-CNRS</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3899-41a83d992c36febf79dabb23108dd4349082dcbff764cd28709698e50c559bfa3</citedby></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=7072206$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7724959$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2960769$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHERWINSKI, H. M</creatorcontrib><creatorcontrib>SCHUMACHER, J. H</creatorcontrib><creatorcontrib>BROWN, K. D</creatorcontrib><creatorcontrib>MOSMANN, T. R</creatorcontrib><title>Two types of mouse helper T cell clone. III: Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies</title><title>The Journal of experimental medicine</title><addtitle>J Exp Med</addtitle><description>Lymphokine synthesis patterns of a panel of 19 T cell clones have been evaluated, using mRNA hybridization methods to examine 11 different mRNAs induced by Con A. The two types of CD4+ Th cell clone described previously were clearly distinguished by this procedure, and the differences between the two types have now been extended to six induced products. With minor exceptions, only Th1 clones synthesized mRNA for IL-2, IFN-gamma, and lymphotoxin, and only Th2 clones synthesized mRNA for IL-4, IL-5, and another induced gene, P600. Four more induced products were expressed preferentially but not uniquely by one or another type of clone: mRNAs for GM-CSF, TNF, and another induced, secreted product (TY5) were produced in larger amounts by Th1 clones, whereas preproenkephalin was preferentially expressed by Th2 clones. IL-3 was produced in similar amounts by both types of clone. mAbs were used to establish three bioassays that were functionally monospecific for IL-2, IL-3, and IL-4, and a new anti-IFN gamma mAb, XMG1.2, was used to establish an ELISA for IFN-gamma. These four assays were used to show that secreted protein and mRNA levels correlated well for all cell lines. The implications of these findings for normal T cells are discussed.</description><subject>Analysis of the immune response. Humoral and cellular immunity</subject><subject>Animals</subject><subject>Antibodies, Monoclonal</subject><subject>Applied sciences</subject><subject>Biological and medical sciences</subject><subject>Biological Assay</subject><subject>Cell Division</subject><subject>Cell Line</subject><subject>Clone Cells - metabolism</subject><subject>Colony-Stimulating Factors - biosynthesis</subject><subject>Enkephalins - biosynthesis</subject><subject>Exact sciences and technology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor</subject><subject>Growth Substances - biosynthesis</subject><subject>Immunobiology</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interleukin-2 - biosynthesis</subject><subject>Interleukin-3 - biosynthesis</subject><subject>Interleukin-4</subject><subject>Interleukin-5</subject><subject>Interleukins - biosynthesis</subject><subject>Lymphokines - biosynthesis</subject><subject>Lymphokines - genetics</subject><subject>Lymphokines - pharmacology</subject><subject>Lymphotoxin-alpha - biosynthesis</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Nucleic Acid Hybridization</subject><subject>Organs and cells involved in the immune response</subject><subject>Other techniques and industries</subject><subject>Protein Precursors - biosynthesis</subject><subject>RNA, Messenger - genetics</subject><subject>T-Lymphocytes, Helper-Inducer - metabolism</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><issn>0022-1007</issn><issn>1540-9538</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk9v1DAQxSMEKkvhyg3JB8SpCbbz1xyQqorCShVIaDlbjj0mLo4d7Gyr8C35RjjsagWnnsbW-83TePyy7CXBBcFd9fYWxoI0TVEXhFL2KNuQusI5q8vucbbBmNKcYNw-zZ7FeIsxqaq6OcvOKGtw27BN9nt379G8TBCR12j0-whoADtBQDskwVokrXdQoO12-w5d78M8JEkZrSGAk6nNOGSXcRr8D-MAxcUlIpqIepjvARzaDQQJp1KlB6-IAtyBsKBQv6Cvny_RsPTBKPNLzMa7C6T3Tq4nYe2SRnI-TiCNNhL1xosYxRIv_lqu2mopbLrOpvfKQHyePdHCRnhxrOfZt-sPu6tP-c2Xj9ury5tclh1jeUVEVyrGqCwbDb1umRJ9T8u0VKWqsmK4o0r2WrdNJRXtWswa1kGNZV2zXovyPHt_8J32_QhKgpuDsHwKZhRh4V4Y_r_izMC_-ztOSceaqkwGb44Gwf_cQ5z5aOK6cuEg_QNv267EaZwHQVJ1XVnXOIHFAZTBxxhAn6YhmK9p4SktPKWF13xNS2p49e8bTvgxHkl_fdRFlMLqIJw08YS1La1Y_TCGW0pxU_4BaHLaJg</recordid><startdate>19871101</startdate><enddate>19871101</enddate><creator>CHERWINSKI, H. M</creator><creator>SCHUMACHER, J. H</creator><creator>BROWN, K. D</creator><creator>MOSMANN, T. R</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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>7T5</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19871101</creationdate><title>Two types of mouse helper T cell clone. III: Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies</title><author>CHERWINSKI, H. M ; SCHUMACHER, J. H ; BROWN, K. D ; MOSMANN, T. R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3899-41a83d992c36febf79dabb23108dd4349082dcbff764cd28709698e50c559bfa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Analysis of the immune response. Humoral and cellular immunity</topic><topic>Animals</topic><topic>Antibodies, Monoclonal</topic><topic>Applied sciences</topic><topic>Biological and medical sciences</topic><topic>Biological Assay</topic><topic>Cell Division</topic><topic>Cell Line</topic><topic>Clone Cells - metabolism</topic><topic>Colony-Stimulating Factors - biosynthesis</topic><topic>Enkephalins - biosynthesis</topic><topic>Exact sciences and technology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor</topic><topic>Growth Substances - biosynthesis</topic><topic>Immunobiology</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interleukin-2 - biosynthesis</topic><topic>Interleukin-3 - biosynthesis</topic><topic>Interleukin-4</topic><topic>Interleukin-5</topic><topic>Interleukins - biosynthesis</topic><topic>Lymphokines - biosynthesis</topic><topic>Lymphokines - genetics</topic><topic>Lymphokines - pharmacology</topic><topic>Lymphotoxin-alpha - biosynthesis</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Nucleic Acid Hybridization</topic><topic>Organs and cells involved in the immune response</topic><topic>Other techniques and industries</topic><topic>Protein Precursors - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>T-Lymphocytes, Helper-Inducer - metabolism</topic><topic>Tumor Necrosis Factor-alpha - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHERWINSKI, H. M</creatorcontrib><creatorcontrib>SCHUMACHER, J. H</creatorcontrib><creatorcontrib>BROWN, K. D</creatorcontrib><creatorcontrib>MOSMANN, T. R</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>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of experimental medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CHERWINSKI, H. M</au><au>SCHUMACHER, J. H</au><au>BROWN, K. D</au><au>MOSMANN, T. R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two types of mouse helper T cell clone. III: Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies</atitle><jtitle>The Journal of experimental medicine</jtitle><addtitle>J Exp Med</addtitle><date>1987-11-01</date><risdate>1987</risdate><volume>166</volume><issue>5</issue><spage>1229</spage><epage>1244</epage><pages>1229-1244</pages><issn>0022-1007</issn><eissn>1540-9538</eissn><coden>JEMEAV</coden><abstract>Lymphokine synthesis patterns of a panel of 19 T cell clones have been evaluated, using mRNA hybridization methods to examine 11 different mRNAs induced by Con A. The two types of CD4+ Th cell clone described previously were clearly distinguished by this procedure, and the differences between the two types have now been extended to six induced products. With minor exceptions, only Th1 clones synthesized mRNA for IL-2, IFN-gamma, and lymphotoxin, and only Th2 clones synthesized mRNA for IL-4, IL-5, and another induced gene, P600. Four more induced products were expressed preferentially but not uniquely by one or another type of clone: mRNAs for GM-CSF, TNF, and another induced, secreted product (TY5) were produced in larger amounts by Th1 clones, whereas preproenkephalin was preferentially expressed by Th2 clones. IL-3 was produced in similar amounts by both types of clone. mAbs were used to establish three bioassays that were functionally monospecific for IL-2, IL-3, and IL-4, and a new anti-IFN gamma mAb, XMG1.2, was used to establish an ELISA for IFN-gamma. These four assays were used to show that secreted protein and mRNA levels correlated well for all cell lines. The implications of these findings for normal T cells are discussed.</abstract><cop>New York, NY</cop><pub>Rockefeller University Press</pub><pmid>2960769</pmid><doi>10.1084/jem.166.5.1229</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis of the immune response. Humoral and cellular immunity Animals Antibodies, Monoclonal Applied sciences Biological and medical sciences Biological Assay Cell Division Cell Line Clone Cells - metabolism Colony-Stimulating Factors - biosynthesis Enkephalins - biosynthesis Exact sciences and technology Fundamental and applied biological sciences. Psychology Fundamental immunology Granulocyte-Macrophage Colony-Stimulating Factor Growth Substances - biosynthesis Immunobiology Interferon-gamma - biosynthesis Interleukin-2 - biosynthesis Interleukin-3 - biosynthesis Interleukin-4 Interleukin-5 Interleukins - biosynthesis Lymphokines - biosynthesis Lymphokines - genetics Lymphokines - pharmacology Lymphotoxin-alpha - biosynthesis Mice Mice, Inbred Strains Nucleic Acid Hybridization Organs and cells involved in the immune response Other techniques and industries Protein Precursors - biosynthesis RNA, Messenger - genetics T-Lymphocytes, Helper-Inducer - metabolism Tumor Necrosis Factor-alpha - biosynthesis |
title | Two types of mouse helper T cell clone. III: Further differences in lymphokine synthesis between Th1 and Th2 clones revealed by RNA hybridization, functionally monospecific bioassays, and monoclonal antibodies |
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