Arsonate-specific murine T cell clones. IV. Properties of I-E- and I-A- restricted clones
The T cell antigen L-tyrosine-p-azobenzenearsonate is unique in being a simple determinant that can be presented in the context of both I-A and I-E. I-E-restricted T cell clones derived from B10.A(5R) mice were found to fall into three groups: Type I clones recognized antigen only in the context of...
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Veröffentlicht in: | The Journal of immunology (1950) 1987-02, Vol.138 (4), p.1169-1177 |
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description | The T cell antigen L-tyrosine-p-azobenzenearsonate is unique in being a simple determinant that can be presented in the context of both I-A and I-E. I-E-restricted T cell clones derived from B10.A(5R) mice were found to fall into three groups: Type I clones recognized antigen only in the context of syngeneic apcs, Type II clones recognized antigen with the same highly specific major histocompatibility complex restriction but in addition proliferated in response to allogeneic stimuli; Type III clones were "degenerate" in their major histocompatibility complex-restricted recognition of antigen and proliferated when antigen-presenting cells bearing Eb beta Ek alpha (syngeneic), Ek beta Ek alpha, or Ed beta Ed alpha were used. These observations allow some conclusions to be drawn about sites on the I-E molecule that may be functionally significant in the presentation of this antigen. By using the B cell hybridoma LK35.2 as target cells, some of these T cell clones act as cytotoxic cells in the Class II-restricted manner predicted from the results of proliferative assays. Class II-restricted cytotoxicity can therefore be controlled by both I-A and I-E mouse Ir gene loci. |
doi_str_mv | 10.4049/jimmunol.138.4.1169 |
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These observations allow some conclusions to be drawn about sites on the I-E molecule that may be functionally significant in the presentation of this antigen. By using the B cell hybridoma LK35.2 as target cells, some of these T cell clones act as cytotoxic cells in the Class II-restricted manner predicted from the results of proliferative assays. Class II-restricted cytotoxicity can therefore be controlled by both I-A and I-E mouse Ir gene loci.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.138.4.1169</identifier><identifier>PMID: 3100628</identifier><identifier>CODEN: JOIMA3</identifier><language>eng</language><publisher>Bethesda, MD: Am Assoc Immnol</publisher><subject>Animals ; Antibodies, Monoclonal - immunology ; Antigen-Presenting Cells - immunology ; Applied sciences ; Azo Compounds - immunology ; Clone Cells - immunology ; Cytotoxicity, Immunologic ; Exact sciences and technology ; Female ; Genes, MHC Class II ; Histocompatibility Antigens - genetics ; Histocompatibility Antigens - immunology ; Histocompatibility Antigens Class II - immunology ; Isoantigens - immunology ; Lymphocyte Activation - drug effects ; Mice ; Mice, Inbred Strains - genetics ; Mice, Inbred Strains - immunology ; Other techniques and industries ; p-Azobenzenearsonate - analogs & derivatives ; p-Azobenzenearsonate - immunology ; p-Azobenzenearsonate - pharmacology ; T-Lymphocytes - immunology ; Tyrosine - analogs & derivatives ; Tyrosine - immunology ; Tyrosine - pharmacology</subject><ispartof>The Journal of immunology (1950), 1987-02, Vol.138 (4), p.1169-1177</ispartof><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3529-858fca4e806596e67a64fd15adfa0b1fd57ca2915d49cf05ddbc1982351fc5c63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7529525$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3100628$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spragg, JH</creatorcontrib><creatorcontrib>Goodman, JW</creatorcontrib><title>Arsonate-specific murine T cell clones. IV. Properties of I-E- and I-A- restricted clones</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>The T cell antigen L-tyrosine-p-azobenzenearsonate is unique in being a simple determinant that can be presented in the context of both I-A and I-E. I-E-restricted T cell clones derived from B10.A(5R) mice were found to fall into three groups: Type I clones recognized antigen only in the context of syngeneic apcs, Type II clones recognized antigen with the same highly specific major histocompatibility complex restriction but in addition proliferated in response to allogeneic stimuli; Type III clones were "degenerate" in their major histocompatibility complex-restricted recognition of antigen and proliferated when antigen-presenting cells bearing Eb beta Ek alpha (syngeneic), Ek beta Ek alpha, or Ed beta Ed alpha were used. These observations allow some conclusions to be drawn about sites on the I-E molecule that may be functionally significant in the presentation of this antigen. By using the B cell hybridoma LK35.2 as target cells, some of these T cell clones act as cytotoxic cells in the Class II-restricted manner predicted from the results of proliferative assays. Class II-restricted cytotoxicity can therefore be controlled by both I-A and I-E mouse Ir gene loci.</description><subject>Animals</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antigen-Presenting Cells - immunology</subject><subject>Applied sciences</subject><subject>Azo Compounds - immunology</subject><subject>Clone Cells - immunology</subject><subject>Cytotoxicity, Immunologic</subject><subject>Exact sciences and technology</subject><subject>Female</subject><subject>Genes, MHC Class II</subject><subject>Histocompatibility Antigens - genetics</subject><subject>Histocompatibility Antigens - immunology</subject><subject>Histocompatibility Antigens Class II - immunology</subject><subject>Isoantigens - immunology</subject><subject>Lymphocyte Activation - drug effects</subject><subject>Mice</subject><subject>Mice, Inbred Strains - genetics</subject><subject>Mice, Inbred Strains - immunology</subject><subject>Other techniques and industries</subject><subject>p-Azobenzenearsonate - analogs & derivatives</subject><subject>p-Azobenzenearsonate - immunology</subject><subject>p-Azobenzenearsonate - pharmacology</subject><subject>T-Lymphocytes - immunology</subject><subject>Tyrosine - analogs & derivatives</subject><subject>Tyrosine - immunology</subject><subject>Tyrosine - pharmacology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtrGzEURkVoSB0nvyAUtCjNShNJo8doaUKSGgzNIi1kJWQ9Gpl5uJIH038fGU9Md13pwj3fp8sB4IbgimGm7jax68Z-aCtSNxWrCBHqDMwI5xgJgcUnMMOYUkSkkJ_BZc4bjLHAlF2Ai5qUkTYz8LpIeejNzqO89TaGaGE3pth7-AKtb1to26H3uYLLXxV8TsPWp130GQ4BLtEDgqZ3ZVggmHzepWh33k2RK3AeTJv99fTOwc_Hh5f772j142l5v1ghW3OqUMObYA3zDRZcCS-kESw4wo0LBq9JcFxaQxXhjikbMHdubYlqaM1JsNyKeg6-HXu3afgzlit0F_PhdNP7YcxaylpyKdV_QcIayrDCBayPoE1DzskHvU2xM-mvJlgfzOsP87qY10wfzJfUl6l-XHfenTKT6rL_Ou1NtqYNyfQ25hMmiwxOecFuj9hb_P22j8nr3Jm2LaVE7_f7fz58B3G-mfg</recordid><startdate>19870215</startdate><enddate>19870215</enddate><creator>Spragg, JH</creator><creator>Goodman, JW</creator><general>Am Assoc Immnol</general><general>American Association of Immunologists</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>H94</scope><scope>7X8</scope></search><sort><creationdate>19870215</creationdate><title>Arsonate-specific murine T cell clones. IV. Properties of I-E- and I-A- restricted clones</title><author>Spragg, JH ; Goodman, JW</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3529-858fca4e806596e67a64fd15adfa0b1fd57ca2915d49cf05ddbc1982351fc5c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antigen-Presenting Cells - immunology</topic><topic>Applied sciences</topic><topic>Azo Compounds - immunology</topic><topic>Clone Cells - immunology</topic><topic>Cytotoxicity, Immunologic</topic><topic>Exact sciences and technology</topic><topic>Female</topic><topic>Genes, MHC Class II</topic><topic>Histocompatibility Antigens - genetics</topic><topic>Histocompatibility Antigens - immunology</topic><topic>Histocompatibility Antigens Class II - immunology</topic><topic>Isoantigens - immunology</topic><topic>Lymphocyte Activation - drug effects</topic><topic>Mice</topic><topic>Mice, Inbred Strains - genetics</topic><topic>Mice, Inbred Strains - immunology</topic><topic>Other techniques and industries</topic><topic>p-Azobenzenearsonate - analogs & derivatives</topic><topic>p-Azobenzenearsonate - immunology</topic><topic>p-Azobenzenearsonate - pharmacology</topic><topic>T-Lymphocytes - immunology</topic><topic>Tyrosine - analogs & derivatives</topic><topic>Tyrosine - immunology</topic><topic>Tyrosine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spragg, JH</creatorcontrib><creatorcontrib>Goodman, JW</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>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spragg, JH</au><au>Goodman, JW</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Arsonate-specific murine T cell clones. IV. Properties of I-E- and I-A- restricted clones</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1987-02-15</date><risdate>1987</risdate><volume>138</volume><issue>4</issue><spage>1169</spage><epage>1177</epage><pages>1169-1177</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>The T cell antigen L-tyrosine-p-azobenzenearsonate is unique in being a simple determinant that can be presented in the context of both I-A and I-E. I-E-restricted T cell clones derived from B10.A(5R) mice were found to fall into three groups: Type I clones recognized antigen only in the context of syngeneic apcs, Type II clones recognized antigen with the same highly specific major histocompatibility complex restriction but in addition proliferated in response to allogeneic stimuli; Type III clones were "degenerate" in their major histocompatibility complex-restricted recognition of antigen and proliferated when antigen-presenting cells bearing Eb beta Ek alpha (syngeneic), Ek beta Ek alpha, or Ed beta Ed alpha were used. These observations allow some conclusions to be drawn about sites on the I-E molecule that may be functionally significant in the presentation of this antigen. By using the B cell hybridoma LK35.2 as target cells, some of these T cell clones act as cytotoxic cells in the Class II-restricted manner predicted from the results of proliferative assays. Class II-restricted cytotoxicity can therefore be controlled by both I-A and I-E mouse Ir gene loci.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>3100628</pmid><doi>10.4049/jimmunol.138.4.1169</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies, Monoclonal - immunology Antigen-Presenting Cells - immunology Applied sciences Azo Compounds - immunology Clone Cells - immunology Cytotoxicity, Immunologic Exact sciences and technology Female Genes, MHC Class II Histocompatibility Antigens - genetics Histocompatibility Antigens - immunology Histocompatibility Antigens Class II - immunology Isoantigens - immunology Lymphocyte Activation - drug effects Mice Mice, Inbred Strains - genetics Mice, Inbred Strains - immunology Other techniques and industries p-Azobenzenearsonate - analogs & derivatives p-Azobenzenearsonate - immunology p-Azobenzenearsonate - pharmacology T-Lymphocytes - immunology Tyrosine - analogs & derivatives Tyrosine - immunology Tyrosine - pharmacology |
title | Arsonate-specific murine T cell clones. IV. Properties of I-E- and I-A- restricted clones |
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