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10.1007/s00115-020-00937-6

http://scihub22266oqcxt.onion/10.1007/s00115-020-00937-6
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32524163!7286209!32524163
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suck abstract from ncbi

pmid32524163      Nervenarzt 2020 ; 91 (8): 722-734
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  • Ocrelizumab zur Behandlung der Multiplen Sklerose #MMPMID32524163
  • Graf J; Albrecht P; Goebels N; Aktas O; Hartung HP
  • Nervenarzt 2020[Aug]; 91 (8): 722-734 PMID32524163show ga
  • Ocrelizumab is a monoclonal antibody directed against the differentiation antigen CD20, which leads to an effective long-term depletion of lymphocytes, in particular B cells. Recently published phase 3 studies confirmed that ocrelizumab is effective in the treatment of both relapsing multiple sclerosis (RMS) and primary progressive multiple sclerosis (PPMS). Based on these results, ocrelizumab was the first drug to be approved for primary chronic progressive MS. To place this therapeutic breakthrough in the context of the current MS therapeutic landscape, it is worthwhile taking a look back at the development of antibody-mediated CD20 depletion, the studies underlying the approval of ocrelizumab and their open extension phases. This review article discusses the available data on the efficacy and safety of long-term B?cell depletion in MS patients and reviews current knowledge on the role of B?lymphocytes in the immunopathogenesis of MS.
  • |*Multiple Sclerosis/drug therapy[MESH]
  • |Antibodies, Monoclonal, Humanized/*therapeutic use[MESH]
  • |Humans[MESH]


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