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T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats

The major encephalitogenic epitope for Lewis rats is the 72-89 sequence of guinea pig basic protein (GP-BP) or rat basic protein (Rt-BP). T cells responsive to this epitope are I-A restricted and preferentially express the V alpha 2:V beta 8 gene combination in their TCR. In this work, we describe f...

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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/PMC2189414/
https://www.ncbi.nlm.nih.gov/pubmed/2474052
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description The major encephalitogenic epitope for Lewis rats is the 72-89 sequence of guinea pig basic protein (GP-BP) or rat basic protein (Rt-BP). T cells responsive to this epitope are I-A restricted and preferentially express the V alpha 2:V beta 8 gene combination in their TCR. In this work, we describe for the first time the delayed appearance of T cells specific for additional discrete determinant of BP, the nonencephalitogenic 55-68 sequence of GP-BP restricted by I-A, and the encephalitogenic 87-99 sequence of Rt-BP restricted by I-E. The TCR V alpha 2:V beta 8 gene combination was expressed by both encephalitogenic GP-BP S72-89 and Rt-BP S87-99 T cell specificities but not by GP-BP 44-68-specific T cells. This is the first demonstration of I-E-restricted encephalitogenic T cells in Lewis rats and supports the conclusion that the I-E class II locus is involved in autoimmune diseases.
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spelling pubmed-21894142008-04-17 T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats J Exp Med Articles The major encephalitogenic epitope for Lewis rats is the 72-89 sequence of guinea pig basic protein (GP-BP) or rat basic protein (Rt-BP). T cells responsive to this epitope are I-A restricted and preferentially express the V alpha 2:V beta 8 gene combination in their TCR. In this work, we describe for the first time the delayed appearance of T cells specific for additional discrete determinant of BP, the nonencephalitogenic 55-68 sequence of GP-BP restricted by I-A, and the encephalitogenic 87-99 sequence of Rt-BP restricted by I-E. The TCR V alpha 2:V beta 8 gene combination was expressed by both encephalitogenic GP-BP S72-89 and Rt-BP S87-99 T cell specificities but not by GP-BP 44-68-specific T cells. This is the first demonstration of I-E-restricted encephalitogenic T cells in Lewis rats and supports the conclusion that the I-E class II locus is involved in autoimmune diseases. The Rockefeller University Press 1989-08-01 /pmc/articles/PMC2189414/ /pubmed/2474052 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
T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats
title T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats
title_full T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats
title_fullStr T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats
title_full_unstemmed T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats
title_short T cell determinants of myelin basic protein include a unique encephalitogenic I-E-restricted epitope for Lewis rats
title_sort t cell determinants of myelin basic protein include a unique encephalitogenic i-e-restricted epitope for lewis rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189414/
https://www.ncbi.nlm.nih.gov/pubmed/2474052