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B cells and plasmablasts in Multiple Sclerosis | 893.72 KB | Adobe PDF |
Advisor(s)
Abstract(s)
Our aim was to quantify circulating B cell subsets; immature/transitional, naïve, CD27- and CD27+ memory cells and plasmablasts, in relapsing-remitting multiple sclerosis patients treated with IFN-β. The most relevant findings were a significant increase of plasmablasts and a decrease of immature/transitional B cells, resulting in a decreased ratio between those cells in relapse RRMS, together with an increase of CD27- and CD27+IgM+ memory B cell subsets in both phases of the disease. These alterations point to an active B cell response, particularly in relapse, and the above referred ratio could constitute a good biomarker of relapse in patients that underwent IFN-β treatment.
Description
Keywords
CD27 Immature/transitional B cell subset Plasmablast Relapsing-remitting multiple sclerosis
Citation
Publisher
Elsevier