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Allospecific Cytotoxic T Lymphocytes Recognize an H-2 Peptide in the Context of a Murine Major Histocompatibility Complex Class I Molecule
We have isolated cytotoxic T lymphocytes (CTL) preferentially reactive with the α 1 external domain of the H-2Ldantigen by selecting for T cells capable of recognizing a variant major histocompatibility complex (MHC) class I antigen sharing α 1 sequences with H-2Ld. Using these CTL, we demonstrate t...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 1988-03, Vol.85 (6), p.1927-1931 |
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container_end_page | 1931 |
container_issue | 6 |
container_start_page | 1927 |
container_title | Proceedings of the National Academy of Sciences - PNAS |
container_volume | 85 |
creator | Song, Elizabeth S. Linsk, Richard Olson, Clifford A. McMillan, Minnie Goodenow, Robert S. |
description | We have isolated cytotoxic T lymphocytes (CTL) preferentially reactive with the α 1 external domain of the H-2Ldantigen by selecting for T cells capable of recognizing a variant major histocompatibility complex (MHC) class I antigen sharing α 1 sequences with H-2Ld. Using these CTL, we demonstrate that a synthetic α 1 peptide corresponding to one of the helices derived from the H-2Ldmolecule can be presented by a class I restriction element to reconstitute a CTL determinant borne by intact H-2Ld. Moreover, several other H-2L-reactive CTL generated independently were also able to recognize H-2Ldeither as an intact alloantigen or as a peptide in conjunction with appropriate class I restriction elements. These data demonstrate that an H-2 peptide can reconstitute a CTL target structure and suggest that some alloreactive T cells in fact might be directed against allogeneic class I peptides in the context of a class I framework. |
doi_str_mv | 10.1073/pnas.85.6.1927 |
format | article |
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Using these CTL, we demonstrate that a synthetic α 1 peptide corresponding to one of the helices derived from the H-2Ldmolecule can be presented by a class I restriction element to reconstitute a CTL determinant borne by intact H-2Ld. Moreover, several other H-2L-reactive CTL generated independently were also able to recognize H-2Ldeither as an intact alloantigen or as a peptide in conjunction with appropriate class I restriction elements. These data demonstrate that an H-2 peptide can reconstitute a CTL target structure and suggest that some alloreactive T cells in fact might be directed against allogeneic class I peptides in the context of a class I framework.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.85.6.1927</identifier><identifier>PMID: 3258067</identifier><identifier>CODEN: PNASA6</identifier><language>eng</language><publisher>Washington, DC: National Academy of Sciences of the United States of America</publisher><subject>Amino Acid Sequence ; Analysis of the immune response. Humoral and cellular immunity ; Animals ; Antigens ; Biological and medical sciences ; Blasts ; Cross Reactions ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; H-2 Antigens - immunology ; Haploidy ; Haplotypes ; Histocompatibility Antigen H-2D ; Immunobiology ; Isoantigens - immunology ; L cells ; Major Histocompatibility Complex ; Major histocompatibility complex genes ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C3H ; Molecular Sequence Data ; Molecular structure ; Molecules ; Organs and cells involved in the immune response ; Reactivity ; Spleen cells ; T lymphocytes ; T-Lymphocytes, Cytotoxic - immunology</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1988-03, Vol.85 (6), p.1927-1931</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3777-a36685675a88a762c3a8ad077dbe63ebd21aac032f982c5e40bfd5394b5f9ce83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/85/6.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/31420$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/31420$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,58237,58470</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7094626$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3258067$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Song, Elizabeth S.</creatorcontrib><creatorcontrib>Linsk, Richard</creatorcontrib><creatorcontrib>Olson, Clifford A.</creatorcontrib><creatorcontrib>McMillan, Minnie</creatorcontrib><creatorcontrib>Goodenow, Robert S.</creatorcontrib><title>Allospecific Cytotoxic T Lymphocytes Recognize an H-2 Peptide in the Context of a Murine Major Histocompatibility Complex Class I Molecule</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>We have isolated cytotoxic T lymphocytes (CTL) preferentially reactive with the α 1 external domain of the H-2Ldantigen by selecting for T cells capable of recognizing a variant major histocompatibility complex (MHC) class I antigen sharing α 1 sequences with H-2Ld. Using these CTL, we demonstrate that a synthetic α 1 peptide corresponding to one of the helices derived from the H-2Ldmolecule can be presented by a class I restriction element to reconstitute a CTL determinant borne by intact H-2Ld. Moreover, several other H-2L-reactive CTL generated independently were also able to recognize H-2Ldeither as an intact alloantigen or as a peptide in conjunction with appropriate class I restriction elements. These data demonstrate that an H-2 peptide can reconstitute a CTL target structure and suggest that some alloreactive T cells in fact might be directed against allogeneic class I peptides in the context of a class I framework.</description><subject>Amino Acid Sequence</subject><subject>Analysis of the immune response. Humoral and cellular immunity</subject><subject>Animals</subject><subject>Antigens</subject><subject>Biological and medical sciences</subject><subject>Blasts</subject><subject>Cross Reactions</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>H-2 Antigens - immunology</subject><subject>Haploidy</subject><subject>Haplotypes</subject><subject>Histocompatibility Antigen H-2D</subject><subject>Immunobiology</subject><subject>Isoantigens - immunology</subject><subject>L cells</subject><subject>Major Histocompatibility Complex</subject><subject>Major histocompatibility complex genes</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C3H</subject><subject>Molecular Sequence Data</subject><subject>Molecular structure</subject><subject>Molecules</subject><subject>Organs and cells involved in the immune response</subject><subject>Reactivity</subject><subject>Spleen cells</subject><subject>T lymphocytes</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNqFkc2L1DAYh4so67h69SAIOYi31iRt83FcyuoszKDIeg5p-tbNkDa1SWHqn-BfbcuM4x4ED-EN_J73A54keU1wRjDPPwy9DpkoM5YRSfmTZEOwJCkrJH6abDCmPBUFLZ4nL0I4YIxlKfBVcpXTpTK-SX7dOOfDAMa21qBqjj764_K7R7u5Gx68mSME9BWM_97bn4B0j7YpRV9giLYBZHsUHwBVvo9wjMi3SKP9NNoe0F4f_Ii2NkRvfDfoaGvrbJwXuBscHFHldAjoDu29AzM5eJk8a7UL8Opcr5NvH2_vq226-_zprrrZpSbnnKc6Z0yUjJdaCM0ZNbkWusGcNzWwHOqGEq0NzmkrBTUlFLhumzKXRV220oDIr5P3p7nD6H9MEKLqbDDgnO7BT0FxQQoiJfsvSApZ8uUtYHYCzehDGKFVw2g7Pc6KYLVaUqslJUrF1GppaXh7njzVHTQX_Kxlyd-dcx2Mdu2oe2PDBeNYFow-PnAd_ye9rFHt5Nzq5dG-f4JL_uaUHxZb499zSEFx_hucS7wd</recordid><startdate>198803</startdate><enddate>198803</enddate><creator>Song, Elizabeth S.</creator><creator>Linsk, Richard</creator><creator>Olson, Clifford A.</creator><creator>McMillan, Minnie</creator><creator>Goodenow, Robert S.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</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>198803</creationdate><title>Allospecific Cytotoxic T Lymphocytes Recognize an H-2 Peptide in the Context of a Murine Major Histocompatibility Complex Class I Molecule</title><author>Song, Elizabeth S. ; Linsk, Richard ; Olson, Clifford A. ; McMillan, Minnie ; Goodenow, Robert S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3777-a36685675a88a762c3a8ad077dbe63ebd21aac032f982c5e40bfd5394b5f9ce83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Amino Acid Sequence</topic><topic>Analysis of the immune response. Humoral and cellular immunity</topic><topic>Animals</topic><topic>Antigens</topic><topic>Biological and medical sciences</topic><topic>Blasts</topic><topic>Cross Reactions</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>H-2 Antigens - immunology</topic><topic>Haploidy</topic><topic>Haplotypes</topic><topic>Histocompatibility Antigen H-2D</topic><topic>Immunobiology</topic><topic>Isoantigens - immunology</topic><topic>L cells</topic><topic>Major Histocompatibility Complex</topic><topic>Major histocompatibility complex genes</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C3H</topic><topic>Molecular Sequence Data</topic><topic>Molecular structure</topic><topic>Molecules</topic><topic>Organs and cells involved in the immune response</topic><topic>Reactivity</topic><topic>Spleen cells</topic><topic>T lymphocytes</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Elizabeth S.</creatorcontrib><creatorcontrib>Linsk, Richard</creatorcontrib><creatorcontrib>Olson, Clifford A.</creatorcontrib><creatorcontrib>McMillan, Minnie</creatorcontrib><creatorcontrib>Goodenow, Robert S.</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>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, Elizabeth S.</au><au>Linsk, Richard</au><au>Olson, Clifford A.</au><au>McMillan, Minnie</au><au>Goodenow, Robert S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Allospecific Cytotoxic T Lymphocytes Recognize an H-2 Peptide in the Context of a Murine Major Histocompatibility Complex Class I Molecule</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1988-03</date><risdate>1988</risdate><volume>85</volume><issue>6</issue><spage>1927</spage><epage>1931</epage><pages>1927-1931</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><coden>PNASA6</coden><abstract>We have isolated cytotoxic T lymphocytes (CTL) preferentially reactive with the α 1 external domain of the H-2Ldantigen by selecting for T cells capable of recognizing a variant major histocompatibility complex (MHC) class I antigen sharing α 1 sequences with H-2Ld. Using these CTL, we demonstrate that a synthetic α 1 peptide corresponding to one of the helices derived from the H-2Ldmolecule can be presented by a class I restriction element to reconstitute a CTL determinant borne by intact H-2Ld. Moreover, several other H-2L-reactive CTL generated independently were also able to recognize H-2Ldeither as an intact alloantigen or as a peptide in conjunction with appropriate class I restriction elements. These data demonstrate that an H-2 peptide can reconstitute a CTL target structure and suggest that some alloreactive T cells in fact might be directed against allogeneic class I peptides in the context of a class I framework.</abstract><cop>Washington, DC</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>3258067</pmid><doi>10.1073/pnas.85.6.1927</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Analysis of the immune response. Humoral and cellular immunity Animals Antigens Biological and medical sciences Blasts Cross Reactions Fundamental and applied biological sciences. Psychology Fundamental immunology H-2 Antigens - immunology Haploidy Haplotypes Histocompatibility Antigen H-2D Immunobiology Isoantigens - immunology L cells Major Histocompatibility Complex Major histocompatibility complex genes Mice Mice, Inbred BALB C Mice, Inbred C3H Molecular Sequence Data Molecular structure Molecules Organs and cells involved in the immune response Reactivity Spleen cells T lymphocytes T-Lymphocytes, Cytotoxic - immunology |
title | Allospecific Cytotoxic T Lymphocytes Recognize an H-2 Peptide in the Context of a Murine Major Histocompatibility Complex Class I Molecule |
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