Mature IgD low/- B cells maintain tolerance by promoting regulatory T cell homeostasis

Abstract

A number of different B cell subsets have been shown to exhibit regulatory activity using a variety of mechanisms to attenuate inflammatory diseases. Here we show, using anti-CD20-mediated partial B cell depletion in mice, that a population of mature B cells distinguishable by IgD low/- expression maintains tolerance by, at least in part, promoting CD4 + Foxp3 + regulatory T cell homeostatic expansion via glucocorticoid-induced tumor necrosis factor receptor ligand, or GITRL. Cell surface phenotyping, transcriptome analysis and developmental study data show that B cells expressing IgD at a low level (BD L ) are a novel population of mature B cells that emerge in the spleen from the transitional-2 stage paralleling the differentiation of follicular B cells. The cell surface phenotype and regulatory function of BD L are highly suggestive that they are a new B cell subset. Human splenic and peripheral blood IgD low/- B cells also exhibit BD L regulatory activity, rendering them of therapeutic interest.