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Ocrelizumab and Other CD20+ B-Cell-Depleting Therapies in Multiple Sclerosis
Jeffrey M Gelfand1, Bruce A C Cree1, Stephen L Hauser2
1Multiple Sclerosis Center, Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.
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.
Insights
Anti-CD20 monoclonal antibodies effectively treat multiple sclerosis (MS) by depleting B cells, reducing inflammation, and slowing disability progression. Ocrelizumab is a key therapy, though infusion reactions, infections, and malignancy risks are noted.
Area of Science:
- Immunology
- Neurology
- Pharmacology
Background:
- Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system.
- Current MS treatments aim to reduce inflammatory relapses and disease progression.
- B cells play a significant role in MS pathogenesis.
Purpose of the Study:
- To review advances in anti-CD20 B-cell-depleting biological therapies for MS.
- To discuss the efficacy and safety of ocrelizumab, rituximab, and ofatumumab in MS treatment.
Main Methods:
- Review of clinical trial data and scientific literature on anti-CD20 therapies in MS.
- Analysis of efficacy in suppressing inflammatory disease activity and disability progression.
- Evaluation of safety profiles, including adverse events and malignancies.
Main Results:
- Anti-CD20 monoclonal antibodies profoundly suppress acute inflammatory disease activity in relapsing-remitting MS.
- Ocrelizumab is the first therapy shown to reduce disability progression in primary progressive MS.
- Common adverse events include infusion reactions and infections; a numerical imbalance in malignancy risk was observed with ocrelizumab.
Conclusions:
- Anti-CD20 B-cell-depleting therapies represent a significant advance in MS treatment.
- Ocrelizumab offers a breakthrough for both relapsing-remitting and primary progressive MS.
- Ongoing monitoring for adverse events, including infections and malignancies, is crucial.
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