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CD20+ T Cells in Multiple Sclerosis: From Pathogenesis to Treatment-Induced Depletion.
Anna Chiara Mazzeo1, Laura Calabresi1, Valentina Damato1,2
1Department of Neurosciences, Psychology, Drug Research and Child Health (NEUROFARBA), University of Florence, 50139 Florence, Italy.
New research highlights CD20+ T cells, a pro-inflammatory subset, as potential drivers of multiple sclerosis (MS) pathology. Their depletion by anti-CD20 therapies may explain treatment efficacy in MS patients.
Area of Science:
- Neuroimmunology
- Cellular Immunology
- Autoimmune Diseases
Background:
- Multiple sclerosis (MS) is traditionally viewed as T cell-mediated.
- Effectiveness of anti-CD20 monoclonal antibodies (mAbs) challenges this, as CD20 is also on T cells.
- CD20+ T cells exhibit pro-inflammatory and CNS-invasive characteristics.
Purpose of the Study:
- To review current knowledge on CD20+ T cells in MS.
- To discuss their identification, characterization, and depletion by disease-modifying treatments (DMTs).
- To explore their pathogenetic role and therapeutic implications in MS.
Main Methods:
- Literature review of clinical and preclinical studies.
- Analysis of data on CD20 expression on T cells in MS patients.
- Examination of the impact of anti-CD20 therapies on CD20+ T cells.
Main Results:
- CD20+ T cells are present in MS brain lesions and experimental models.
- These cells show increased pro-inflammatory and migratory potential.
- Depletion of CD20+ T cells by DMTs is observed in MS patients.
Conclusions:
- CD20+ T cells are implicated in MS pathogenesis.
- Their depletion likely contributes to the efficacy of anti-CD20 therapies.
- Further research is needed to clarify their origin and precise role.
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