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Identical peptides recognized by MHC class I- and II-restricted T cells

Previous data from many groups show that both class I and class II- restricted T cells recognize short synthetic peptides in the context of their respective MHC molecules (9-18), all of the peptides described to date are restricted to only a single class of MHC molecules; however, structural homolog...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189383/
https://www.ncbi.nlm.nih.gov/pubmed/2501446
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description Previous data from many groups show that both class I and class II- restricted T cells recognize short synthetic peptides in the context of their respective MHC molecules (9-18), all of the peptides described to date are restricted to only a single class of MHC molecules; however, structural homology between the class I and II MHC molecules and the use of similar TCRs by class I and II-restricted T cells suggest that antigen recognition mechanisms are similar in both systems. To directly compare antigen recognition in the two systems, we analyzed peptides for the ability to function in both a class I and II-restricted system and found that seven of seven individual peptides tested stimulate both class I and II-restricted T cell responses. In addition, two of the peptides can function in different species stimulating both human class I and murine class II T cell responses. Thus, the process of T cell recognition of antigen in the context of MHC molecules was highly conserved in evolution not only between the class I and class II MHC systems, but also between the murine and human species.
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spelling pubmed-21893832008-04-17 Identical peptides recognized by MHC class I- and II-restricted T cells J Exp Med Articles Previous data from many groups show that both class I and class II- restricted T cells recognize short synthetic peptides in the context of their respective MHC molecules (9-18), all of the peptides described to date are restricted to only a single class of MHC molecules; however, structural homology between the class I and II MHC molecules and the use of similar TCRs by class I and II-restricted T cells suggest that antigen recognition mechanisms are similar in both systems. To directly compare antigen recognition in the two systems, we analyzed peptides for the ability to function in both a class I and II-restricted system and found that seven of seven individual peptides tested stimulate both class I and II-restricted T cell responses. In addition, two of the peptides can function in different species stimulating both human class I and murine class II T cell responses. Thus, the process of T cell recognition of antigen in the context of MHC molecules was highly conserved in evolution not only between the class I and class II MHC systems, but also between the murine and human species. The Rockefeller University Press 1989-07-01 /pmc/articles/PMC2189383/ /pubmed/2501446 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
Identical peptides recognized by MHC class I- and II-restricted T cells
title Identical peptides recognized by MHC class I- and II-restricted T cells
title_full Identical peptides recognized by MHC class I- and II-restricted T cells
title_fullStr Identical peptides recognized by MHC class I- and II-restricted T cells
title_full_unstemmed Identical peptides recognized by MHC class I- and II-restricted T cells
title_short Identical peptides recognized by MHC class I- and II-restricted T cells
title_sort identical peptides recognized by mhc class i- and ii-restricted t cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189383/
https://www.ncbi.nlm.nih.gov/pubmed/2501446