| Literature DB >> 28695471 |
Jeffrey M Gelfand1, Bruce A C Cree1, Stephen L Hauser2.
Abstract
Selective depletion of CD20+ B cells by anti-CD20 monoclonal antibodies as monotherapy in multiple sclerosis (MS) profoundly suppresses acute inflammatory disease activity and signifies an important advance in the treatment of relapsing-remitting MS. Ocrelizumab, a humanized anti-CD20 monoclonal antibody, is also the first proven therapy to lessen disability progression in primary progressive MS-a breakthrough for patients with a disease that had no proven therapy. Ocrelizumab is generally well tolerated, with the most common adverse events experienced being infusion reactions and infections. In ocrelizumab trials in MS a numerical imbalance in the risk of malignancies was observed. In this article, we review advances in anti-CD20 B-cell-depleting biological therapies for MS, including ocrelizumab, rituximab, and ofatumumab.Entities:
Keywords: B-cell-depleting therapy; Multiple sclerosis; ocrelizumab; progressive MS; relapsing-remitting MS; rituximab
Mesh:
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Year: 2017 PMID: 28695471 PMCID: PMC5722762 DOI: 10.1007/s13311-017-0557-4
Source DB: PubMed Journal: Neurotherapeutics ISSN: 1878-7479 Impact factor: 7.620