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A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis

Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS) characterized by plaques of infiltrating CD4(+) and CD8(+) T cells. Studies of MS and experimental autoimmune encephalomyelitis (EAE), an animal model of MS, focus on the contribution of CD4(+) myelin-specific T c...

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Autores principales: Huseby, Eric S., Liggitt, Denny, Brabb, Thea, Schnabel, Bryan, Öhlén, Claes, Goverman, Joan
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195947/
https://www.ncbi.nlm.nih.gov/pubmed/11535634
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author Huseby, Eric S.
Liggitt, Denny
Brabb, Thea
Schnabel, Bryan
Öhlén, Claes
Goverman, Joan
author_facet Huseby, Eric S.
Liggitt, Denny
Brabb, Thea
Schnabel, Bryan
Öhlén, Claes
Goverman, Joan
author_sort Huseby, Eric S.
collection PubMed
description Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS) characterized by plaques of infiltrating CD4(+) and CD8(+) T cells. Studies of MS and experimental autoimmune encephalomyelitis (EAE), an animal model of MS, focus on the contribution of CD4(+) myelin-specific T cells. The role of CD8(+) myelin-specific T cells in mediating EAE or MS has not been described previously. Here, we demonstrate that myelin-specific CD8(+) T cells induce severe CNS autoimmunity in mice. The pathology and clinical symptoms in CD8(+) T cell–mediated CNS autoimmunity demonstrate similarities to MS not seen in myelin-specific CD4(+) T cell–mediated EAE. These data suggest that myelin-specific CD8(+) T cells could function as effector cells in the pathogenesis of MS.
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spelling pubmed-21959472008-04-14 A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis Huseby, Eric S. Liggitt, Denny Brabb, Thea Schnabel, Bryan Öhlén, Claes Goverman, Joan J Exp Med Original Article Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS) characterized by plaques of infiltrating CD4(+) and CD8(+) T cells. Studies of MS and experimental autoimmune encephalomyelitis (EAE), an animal model of MS, focus on the contribution of CD4(+) myelin-specific T cells. The role of CD8(+) myelin-specific T cells in mediating EAE or MS has not been described previously. Here, we demonstrate that myelin-specific CD8(+) T cells induce severe CNS autoimmunity in mice. The pathology and clinical symptoms in CD8(+) T cell–mediated CNS autoimmunity demonstrate similarities to MS not seen in myelin-specific CD4(+) T cell–mediated EAE. These data suggest that myelin-specific CD8(+) T cells could function as effector cells in the pathogenesis of MS. The Rockefeller University Press 2001-09-03 /pmc/articles/PMC2195947/ /pubmed/11535634 Text en © 2001 The Rockefeller University Press 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 Original Article
Huseby, Eric S.
Liggitt, Denny
Brabb, Thea
Schnabel, Bryan
Öhlén, Claes
Goverman, Joan
A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis
title A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis
title_full A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis
title_fullStr A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis
title_full_unstemmed A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis
title_short A Pathogenic Role for Myelin-Specific Cd8(+) T Cells in a Model for Multiple Sclerosis
title_sort pathogenic role for myelin-specific cd8(+) t cells in a model for multiple sclerosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195947/
https://www.ncbi.nlm.nih.gov/pubmed/11535634
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