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B Cells and Autoantibodies in Multiple Sclerosis
JournalItem (Reviews, Editorials, Rezensionen, Urteilsanmerkungen etc. in einer wissenschaftlichen Zeitschrift)
 
ID 4378943
Author(s) Probstel, A. K.; Sanderson, N. S.; Derfuss, T.
Author(s) at UniBasel Derfuss, Tobias Johannes
Year 2015
Title B Cells and Autoantibodies in Multiple Sclerosis
Journal International Journal of Molecular Sciences
Volume 16
Number 7
Pages 16576-92
Keywords Animals; Autoantibodies/*immunology; B-Lymphocytes/*immunology; Humans; Immunotherapy/methods; Multiple Sclerosis/etiology/*immunology/therapy; Precision Medicine/methods; B cells; autoantibodies; autoantigen; multiple sclerosis; neuromyelitis optica; pathogenesis; therapy
Mesh terms Animals; Autoantibodies, immunology; B-Lymphocytes, immunology; Humans; Immunotherapy, methods; Multiple Sclerosis, therapy; Precision Medicine, methods
Abstract 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.
Publisher Molecular Diversity Preservation International (MDPI)
ISSN/ISBN 1422-0067
URL https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4519967/
edoc-URL https://edoc.unibas.ch/61678/
Full Text on edoc No
Digital Object Identifier DOI 10.3390/ijms160716576
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/26197319
ISI-Number WOS:000359900100126
Document type (ISI) Journal Article, Review
 
   

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14/05/2024