| Literature DB >> 30632834 |
Kjell-Morten Myhr1,2, Øivind Torkildsen1,2, Andreas Lossius3,4, Lars Bø1,2, Trygve Holmøy3,5.
Abstract
INTRODUCTION: Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system. The latest development of B-cell depletion by anti-CD20 monoclonal antibodies has been a large step forward in the treatment of this devastating disease. AREAS COVERED: In this manuscript, we review mechanisms of action, efficacy, safety, and tolerance of anti-CD20 therapies for MS, including rituximab, ocrelizumab, and ofatumumab. EXPERT OPINION: B-cell depletion efficiently suppresses acute inflammatory disease activity in relapsing-remitting MS (RRMS), and may slowdown progression in primary progressive MS (PPMS). The treatment is generally well tolerated, with manageable adverse events related to infusion reactions and infections. Ocrelizumab, a humanized anti-CD20 monoclonal antibody, is the first therapy to be approved for the treatment of both RRMS and PPMS.Entities:
Keywords: B cell; Multiple sclerosis; anti-CD20 antibody; ocrelizumab; ofatumumab; rituximab; treatment
Mesh:
Substances:
Year: 2019 PMID: 30632834 DOI: 10.1080/14712598.2019.1568407
Source DB: PubMed Journal: Expert Opin Biol Ther ISSN: 1471-2598 Impact factor: 4.388