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Advancing Treatment in Pediatric Multiple Sclerosis: The Promise of B-Cell-Targeting Therapies
Charalampos Skarlis1, Maria Kotsari1, Maria Anagnostouli1,2
1Research Immunogenetics Laboratory, First Department of Neurology, School of Medicine, National and Kapodistrian University of Athens, Aeginition University Hospital, Vas. Sofias 72-74, 11528 Athens, Greece.
Insights
Pediatric-onset multiple sclerosis (POMS) involves significant inflammation and frequent relapses. Early use of B-cell therapies, like anti-CD20 agents, shows promise for treating this rare central nervous system disease.
Area of Science:
- Neuroimmunology
- Demyelinating Diseases
Background:
- Pediatric-onset multiple sclerosis (POMS) is a rare central nervous system demyelinating disease.
- POMS exhibits a more inflammatory disease course and higher relapse rates than adult-onset MS (AOMS).
- Early intervention with high-efficacy disease-modifying therapies (DMTs) is crucial to prevent neurological damage in POMS.
Purpose of the Study:
- To review the role of B-cells in POMS pathophysiology.
- To evaluate the therapeutic potential of anti-CD20 monoclonal antibodies for POMS.
- To discuss emerging B-cell-directed therapies and future treatment strategies for POMS.
Main Methods:
- Literature review of current knowledge on POMS.
- Analysis of B-cell involvement in POMS pathogenesis.
- Evaluation of anti-CD20 therapies and other novel B-cell-targeting agents.
Main Results:
- B-cells play a significant role in the immunopathogenesis of POMS.
- Anti-CD20 monoclonal antibodies demonstrate therapeutic potential for POMS, similar to their efficacy in adult MS.
- Several novel B-cell-directed therapies are under investigation for POMS.
Conclusions:
- B-cell-targeting therapies, particularly anti-CD20 agents, represent a promising treatment avenue for POMS.
- Early initiation of effective DMTs is essential for managing POMS.
- Future research should focus on novel B-cell-directed approaches like anti-CD19 therapies, BTK inhibitors, and BAFF-targeting agents for POMS.
Abstract:
Pediatric-onset multiple sclerosis (POMS) is a rare yet increasingly recognized demyelinating disease of the central nervous system, characterized by a highly inflammatory disease course and an elevated relapse rate compared to adult-onset MS (AOMS). Given the unique immunopathogenesis of POMS, recent therapeutic strategies have shifted toward early initiation of high-efficacy disease-modifying therapies (DMTs) to minimize irreversible neurological damage. Among these, B-cell-targeting therapies, particularly anti-CD20 monoclonal antibodies, have shown efficacy in adult MS and are emerging as promising candidates for POMS treatment. The present review summarizes the current knowledge of the role of B-cells in POMS pathophysiology and evaluates the therapeutic potential of anti-CD-20 agents. It also highlights ongoing clinical trials and future perspectives, including novel B-cell-directed approaches such as anti-CD19 therapies, Bruton's tyrosine kinase (BTK) inhibitors, and BAFF-targeting agents.
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