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Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen
Cloned CTLs QM3 and QM7 isolated from a bulk CTL line B10.QBR anti- B10.MBR recognized a combination of the H-2Kb molecule and an I-Ak subregion gene product. Such a combinatorial specificity was revealed by complementation of the target antigen in F1 animals between two negative parental strains ca...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1986
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188072/ https://www.ncbi.nlm.nih.gov/pubmed/3485175 |
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collection | PubMed |
description | Cloned CTLs QM3 and QM7 isolated from a bulk CTL line B10.QBR anti- B10.MBR recognized a combination of the H-2Kb molecule and an I-Ak subregion gene product. Such a combinatorial specificity was revealed by complementation of the target antigen in F1 animals between two negative parental strains carrying H-2Kb and I-Ak, respectively. We confirmed the involvement of the H-2Kb molecule by blocking killing with anti-Kb mAb and failure of certain mutant H-2Kb genes to complement with I-Ak to generate the determinant in F1 animals. Although the nature of the I-Ak subregion gene product is not definitive, there was a correlation between the expression of Ia antigens on the cell surface and susceptibility of the cells to lysis by these CTLs, suggesting that it is the classical I-Ak class II antigen. |
format | Text |
id | pubmed-2188072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1986 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21880722008-04-17 Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen J Exp Med Articles Cloned CTLs QM3 and QM7 isolated from a bulk CTL line B10.QBR anti- B10.MBR recognized a combination of the H-2Kb molecule and an I-Ak subregion gene product. Such a combinatorial specificity was revealed by complementation of the target antigen in F1 animals between two negative parental strains carrying H-2Kb and I-Ak, respectively. We confirmed the involvement of the H-2Kb molecule by blocking killing with anti-Kb mAb and failure of certain mutant H-2Kb genes to complement with I-Ak to generate the determinant in F1 animals. Although the nature of the I-Ak subregion gene product is not definitive, there was a correlation between the expression of Ia antigens on the cell surface and susceptibility of the cells to lysis by these CTLs, suggesting that it is the classical I-Ak class II antigen. The Rockefeller University Press 1986-04-01 /pmc/articles/PMC2188072/ /pubmed/3485175 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen |
title | Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen |
title_full | Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen |
title_fullStr | Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen |
title_full_unstemmed | Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen |
title_short | Cloned cytotoxic T lymphocytes that recognize an I-A region product in the context of a class I antigen |
title_sort | cloned cytotoxic t lymphocytes that recognize an i-a region product in the context of a class i antigen |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188072/ https://www.ncbi.nlm.nih.gov/pubmed/3485175 |