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Activation of autoreactive T cells by peptides from human pathogens

Activation of autoreactive T cells is a necessary — but not sufficient — step in the development of T cell mediated autoimmunity. Autoreactive T cells can be activated by viral and bacterial peptides that meet the structural requirements for MHC molecule binding and T cell receptor recognition. Due...

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Detalles Bibliográficos
Autores principales: Hausmann, Stefan, Wucherpfennig, Kai W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134830/
https://www.ncbi.nlm.nih.gov/pubmed/9492986
http://dx.doi.org/10.1016/S0952-7915(97)80186-0
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author Hausmann, Stefan
Wucherpfennig, Kai W
author_facet Hausmann, Stefan
Wucherpfennig, Kai W
author_sort Hausmann, Stefan
collection PubMed
description Activation of autoreactive T cells is a necessary — but not sufficient — step in the development of T cell mediated autoimmunity. Autoreactive T cells can be activated by viral and bacterial peptides that meet the structural requirements for MHC molecule binding and T cell receptor recognition. Due to the degenerate nature of MHC class II molecule binding motifs and a certain degree of flexibility in T cell receptor recognition, such microbial peptides have been found to be quite distinct in their primary sequence from the self-peptide they mimic.
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spelling pubmed-71348302020-04-08 Activation of autoreactive T cells by peptides from human pathogens Hausmann, Stefan Wucherpfennig, Kai W Curr Opin Immunol Article Activation of autoreactive T cells is a necessary — but not sufficient — step in the development of T cell mediated autoimmunity. Autoreactive T cells can be activated by viral and bacterial peptides that meet the structural requirements for MHC molecule binding and T cell receptor recognition. Due to the degenerate nature of MHC class II molecule binding motifs and a certain degree of flexibility in T cell receptor recognition, such microbial peptides have been found to be quite distinct in their primary sequence from the self-peptide they mimic. Published by Elsevier Ltd. 1997-12 2002-02-11 /pmc/articles/PMC7134830/ /pubmed/9492986 http://dx.doi.org/10.1016/S0952-7915(97)80186-0 Text en Copyright © 1997 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Hausmann, Stefan
Wucherpfennig, Kai W
Activation of autoreactive T cells by peptides from human pathogens
title Activation of autoreactive T cells by peptides from human pathogens
title_full Activation of autoreactive T cells by peptides from human pathogens
title_fullStr Activation of autoreactive T cells by peptides from human pathogens
title_full_unstemmed Activation of autoreactive T cells by peptides from human pathogens
title_short Activation of autoreactive T cells by peptides from human pathogens
title_sort activation of autoreactive t cells by peptides from human pathogens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134830/
https://www.ncbi.nlm.nih.gov/pubmed/9492986
http://dx.doi.org/10.1016/S0952-7915(97)80186-0
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