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Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses

Recognition of conventional foreign antigen by T cells is determined by the expression of multiple variable regions of both alpha and beta chains of the T cell receptor (TCR) alpha/beta heterodimer. In contrast, there exists a class of antigens that appears to interact with the TCR alpha/beta hetero...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119212/
https://www.ncbi.nlm.nih.gov/pubmed/1533244
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description Recognition of conventional foreign antigen by T cells is determined by the expression of multiple variable regions of both alpha and beta chains of the T cell receptor (TCR) alpha/beta heterodimer. In contrast, there exists a class of antigens that appears to interact with the TCR alpha/beta heterodimer through the variable region on the beta chain (V beta), independent of other TCR components, a property that has led to their designation as superantigens. The goal of the present study was to analyze V alpha use in V beta 6+ T cells responsive to the superantigen, Mlaa. Results indicate that while deletion of T cells expressing V beta 6 in Mlsa-expressing mice is essentially complete and therefore appears to occur regardless of V alpha usage, in vitro Mlsa stimulation of T cells from Mlsa-negative mice results in significant skewing of V alpha use among responding V beta 6+ T cells. This indicates that V alpha expression influences recognition of the superantigen, Mlsa by mature peripheral T cells.
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spelling pubmed-21192122008-04-16 Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses J Exp Med Articles Recognition of conventional foreign antigen by T cells is determined by the expression of multiple variable regions of both alpha and beta chains of the T cell receptor (TCR) alpha/beta heterodimer. In contrast, there exists a class of antigens that appears to interact with the TCR alpha/beta heterodimer through the variable region on the beta chain (V beta), independent of other TCR components, a property that has led to their designation as superantigens. The goal of the present study was to analyze V alpha use in V beta 6+ T cells responsive to the superantigen, Mlaa. Results indicate that while deletion of T cells expressing V beta 6 in Mlsa-expressing mice is essentially complete and therefore appears to occur regardless of V alpha usage, in vitro Mlsa stimulation of T cells from Mlsa-negative mice results in significant skewing of V alpha use among responding V beta 6+ T cells. This indicates that V alpha expression influences recognition of the superantigen, Mlsa by mature peripheral T cells. The Rockefeller University Press 1992-05-01 /pmc/articles/PMC2119212/ /pubmed/1533244 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
Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses
title Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses
title_full Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses
title_fullStr Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses
title_full_unstemmed Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses
title_short Influence of T cell receptor V alpha expression on Mlsa superantigen- specific T cell responses
title_sort influence of t cell receptor v alpha expression on mlsa superantigen- specific t cell responses
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119212/
https://www.ncbi.nlm.nih.gov/pubmed/1533244