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B Cells and Autoantibodies in Multiple Sclerosis

While over the past decades T cells have been considered key players in the pathogenesis of multiple sclerosis (MS), it has only recently become evident that B cells have a major contributing role. Our understanding of the role of B cells has evolved substantially following the clinical success of B...

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Detalles Bibliográficos
Autores principales: Pröbstel, Anne-Katrin, Sanderson, Nicholas S. R., Derfuss, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519967/
https://www.ncbi.nlm.nih.gov/pubmed/26197319
http://dx.doi.org/10.3390/ijms160716576
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author Pröbstel, Anne-Katrin
Sanderson, Nicholas S. R.
Derfuss, Tobias
author_facet Pröbstel, Anne-Katrin
Sanderson, Nicholas S. R.
Derfuss, Tobias
author_sort Pröbstel, Anne-Katrin
collection PubMed
description While over the past decades T cells have been considered key players in the pathogenesis of multiple sclerosis (MS), it has only recently become evident that B cells have a major contributing role. Our understanding of the role of B cells has evolved substantially following the clinical success of B cell-targeting therapies and increasing experimental evidence for significant B cell involvement. Rather than mere antibody-producing cells, it is becoming clear that they are team players with the capacity to prime and regulate T cells, and function both as pro- and anti-inflammatory mediators. However, despite tremendous efforts, the target antigen(s) of B cells in MS have yet to be identified. The first part of this review summarizes the clinical evidence and results from animal studies pointing to the relevance of B cells in the pathogenesis of MS. The second part gives an overview of the currently known potential autoantigen targets. The third part recapitulates and critically appraises the currently available B cell-directed therapies.
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spelling pubmed-45199672015-08-03 B Cells and Autoantibodies in Multiple Sclerosis Pröbstel, Anne-Katrin Sanderson, Nicholas S. R. Derfuss, Tobias Int J Mol Sci Review While over the past decades T cells have been considered key players in the pathogenesis of multiple sclerosis (MS), it has only recently become evident that B cells have a major contributing role. Our understanding of the role of B cells has evolved substantially following the clinical success of B cell-targeting therapies and increasing experimental evidence for significant B cell involvement. Rather than mere antibody-producing cells, it is becoming clear that they are team players with the capacity to prime and regulate T cells, and function both as pro- and anti-inflammatory mediators. However, despite tremendous efforts, the target antigen(s) of B cells in MS have yet to be identified. The first part of this review summarizes the clinical evidence and results from animal studies pointing to the relevance of B cells in the pathogenesis of MS. The second part gives an overview of the currently known potential autoantigen targets. The third part recapitulates and critically appraises the currently available B cell-directed therapies. MDPI 2015-07-21 /pmc/articles/PMC4519967/ /pubmed/26197319 http://dx.doi.org/10.3390/ijms160716576 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pröbstel, Anne-Katrin
Sanderson, Nicholas S. R.
Derfuss, Tobias
B Cells and Autoantibodies in Multiple Sclerosis
title B Cells and Autoantibodies in Multiple Sclerosis
title_full B Cells and Autoantibodies in Multiple Sclerosis
title_fullStr B Cells and Autoantibodies in Multiple Sclerosis
title_full_unstemmed B Cells and Autoantibodies in Multiple Sclerosis
title_short B Cells and Autoantibodies in Multiple Sclerosis
title_sort b cells and autoantibodies in multiple sclerosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519967/
https://www.ncbi.nlm.nih.gov/pubmed/26197319
http://dx.doi.org/10.3390/ijms160716576
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