Anti-CD20 MONOCLONAL ANTIBODIES IN THE TREATMENT OF MULTIPLE SCLEROSIS: MECHANISMS OF ACTION, CLINICAL EFFICACY, SAFETY, AND CONTEMPORARY THERAPEUTIC PERSPECTIVES

Authors

DOI:

https://doi.org/10.31435/ijitss.3(51).2026.6456

Keywords:

Multiple Sclerosis, Anti-CD20, B Cells, Ocrelizumab, Ofatumumab, Rituximab, Ublituximab, Monoclonal Antibodies, Disease-modifying Therapy, Safety

Abstract

Multiple sclerosis (MS) is a chronic immune-mediated disease of the central nervous system in which B lymphocytes play a central role in disease pathogenesis. The development of anti-CD20 monoclonal antibodies has transformed the therapeutic landscape of MS by providing highly effective disease-modifying therapies with sustained reductions in relapse activity, magnetic resonance imaging disease activity, and disability progression. This review summarizes the current evidence regarding the biological rationale for B-cell depletion and discusses the mechanisms of action, efficacy, safety, and clinical applications of rituximab, ocrelizumab, ofatumumab, and ublituximab. Particular attention is given to adverse events, including infusion- and injection-related reactions, infections, hypogammaglobulinemia, vaccine responsiveness, and long-term monitoring strategies. Current treatment recommendations and the evolving role of anti-CD20 therapies within contemporary MS management are also reviewed. Overall, anti-CD20 monoclonal antibodies represent a cornerstone of modern MS therapy, offering substantial clinical benefit when combined with individualized patient selection, appropriate monitoring, and preventive measures.

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Published

2026-09-21

How to Cite

Kałwik, M., Klepacz, I., Mikołajczak , P. ., Szwarc , T. ., Groth, D. ., Dubiel , W. ., Lorent, A. ., & Rykowska, M. . (2026). Anti-CD20 MONOCLONAL ANTIBODIES IN THE TREATMENT OF MULTIPLE SCLEROSIS: MECHANISMS OF ACTION, CLINICAL EFFICACY, SAFETY, AND CONTEMPORARY THERAPEUTIC PERSPECTIVES. International Journal of Innovative Technologies in Social Science, 4(3(51). https://doi.org/10.31435/ijitss.3(51).2026.6456

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