The role of CD20⁺ T cells: Insights in human peripheral blood

CD20(+) T cells constitute a small subset of T cells. These are found among CD4(+), CD8(+), CD4(+)CD8(+), CD4(-)CD8(-) T, and TCR gamma delta(+) T cells, and have been poorly characterized. The aim of this study was to characterize peripheral blood (PB) CD20(+) T cells and compare them to their PB CD20(-) T cell counterparts. PB from 17 healthy individuals was collected. The distribution of CD20(+) T cells among maturation-associated T cells compartments (na & iuml;ve, central memory, transitional memory, effector memory, and effector T cells), their polarization, activation status, and expression of immune-regulatory proteins were evaluated by flow cytometry. Their function was also assessed, by measuring IFN-gamma, TNF-alpha, and IL-17 production. Compared with CD20(-) T cells, CD20(+) T cells represent a higher proportion of transitional memory cells. Furthermore, CD20(+) T cells display a proinflammatory phenotype, characterized by the expansion of Th1, Th1/17, and Tc1 cell subsets , associated to a high expression of activation (CD25) and exhaustion (PD-1) markers. In addition, the simultaneous production of the proinflammatory cytokines IFN-gamma, TNF-alpha, and IL-17 was also detected in CD4(+)CD20(+) T cells. Our results show that CD20(+) T cells are phenotypically and functionally different from CD20(-) T cells, suggesting that these cells are a distinct subset of T cells.