| Literature DB >> 31130183 |
Austin Negron1, Rachel R Robinson1, Olaf Stüve2, Thomas G Forsthuber3.
Abstract
While it was long held that T cells were the primary mediators of multiple sclerosis (MS) pathogenesis, the beneficial effects observed in response to treatment with Rituximab (RTX), a monoclonal antibody (mAb) targeting CD20, shed light on a key contributor to MS that had been previously underappreciated: B cells. This has been reaffirmed by results from clinical trials testing the efficacy of subsequently developed B cell-depleting mAbs targeting CD20 as well as studies revisiting the effects of previous disease-modifying therapies (DMTs) on B cell subsets thought to modulate disease severity. In this review, we summarize current knowledge regarding the complex roles of B cells in MS pathogenesis and current and potential future B cell-directed therapies.Entities:
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Year: 2018 PMID: 31130183 PMCID: PMC6540809 DOI: 10.1016/j.cellimm.2018.10.006
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868