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The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models

Autoreactive CD4+ T cells, which target antigens in central nervous system (CNS) myelin, are widely believed to play a critical role in the pathogenesis of multiple sclerosis (MS) in concert with other immune effectors. This theory is supported by data from animal model experiments, genome-wide asso...

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Detalles Bibliográficos
Autor principal: Segal, Benjamin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352150/
https://www.ncbi.nlm.nih.gov/pubmed/30669462
http://dx.doi.org/10.3390/jcm8010120
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author Segal, Benjamin M.
author_facet Segal, Benjamin M.
author_sort Segal, Benjamin M.
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description Autoreactive CD4+ T cells, which target antigens in central nervous system (CNS) myelin, are widely believed to play a critical role in the pathogenesis of multiple sclerosis (MS) in concert with other immune effectors. This theory is supported by data from animal model experiments, genome-wide association studies, and immune profiles of individuals with MS. Furthermore, disease modifying agents that target lymphocytes significantly reduce the rate of MS clinical exacerbations. However, the properties of myelin-reactive CD4+ T cells that are critical for their pathogenic activities are not understood completely. This article reviews the literature on encephalitogenic CD4+ T cells, with an emphasis on T-helper (Th) lineage and cytokine production. An increased understanding of the spectrum of encephalitogenic T cells and how they differ from protective subsets is necessary for the development of the next generation of more effective and safer immunomodulatory therapies customized for individuals with MS and related disorders.
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spelling pubmed-63521502019-02-01 The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models Segal, Benjamin M. J Clin Med Review Autoreactive CD4+ T cells, which target antigens in central nervous system (CNS) myelin, are widely believed to play a critical role in the pathogenesis of multiple sclerosis (MS) in concert with other immune effectors. This theory is supported by data from animal model experiments, genome-wide association studies, and immune profiles of individuals with MS. Furthermore, disease modifying agents that target lymphocytes significantly reduce the rate of MS clinical exacerbations. However, the properties of myelin-reactive CD4+ T cells that are critical for their pathogenic activities are not understood completely. This article reviews the literature on encephalitogenic CD4+ T cells, with an emphasis on T-helper (Th) lineage and cytokine production. An increased understanding of the spectrum of encephalitogenic T cells and how they differ from protective subsets is necessary for the development of the next generation of more effective and safer immunomodulatory therapies customized for individuals with MS and related disorders. MDPI 2019-01-19 /pmc/articles/PMC6352150/ /pubmed/30669462 http://dx.doi.org/10.3390/jcm8010120 Text en © 2019 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Segal, Benjamin M.
The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models
title The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models
title_full The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models
title_fullStr The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models
title_full_unstemmed The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models
title_short The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models
title_sort diversity of encephalitogenic cd4+ t cells in multiple sclerosis and its animal models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352150/
https://www.ncbi.nlm.nih.gov/pubmed/30669462
http://dx.doi.org/10.3390/jcm8010120
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