| Literature DB >> 25783157 |
Hyuk Soon Kim1, A-Ram Kim1, Do Kyun Kim1, Hyun Woo Kim1, Young Hwan Park1, Geun Hyo Jang1, Bokyung Kim1, Yeong Min Park1, Jueng Soo You1, Hyung Sik Kim2, Michael A Beaven3, Young Mi Kim4, Wahn Soo Choi5.
Abstract
Subsets of B cells inhibit various immune responses through their production of the cytokine interleukin-10 (IL-10). We found that IL-10-producing CD5(+) B cells suppressed the immunoglobulin E (IgE)- and antigen-mediated activation of mast cells in vitro as well as allergic responses in mice in an IL-10-dependent manner. Furthermore, the suppressive effect of these B cells on mast cells in vitro and in vivo depended on direct cell-to-cell contact through the costimulatory receptor CD40 on CD5(+) B cells and the CD40 ligand on mast cells. This contact enhanced the production of IL-10 by the CD5(+) B cells. Through activation of the Janus-activated kinase-signal transducer and activator of transcription 3 pathway, IL-10 decreased the abundance of the kinases Fyn and Fgr and inhibited the activation of the downstream kinase Syk in mast cells. Together, these findings suggest that an important function of IL-10-producing CD5(+) B cells is inhibiting mast cells and IgE-mediated allergic responses.Entities:
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Year: 2015 PMID: 25783157 DOI: 10.1126/scisignal.2005861
Source DB: PubMed Journal: Sci Signal ISSN: 1945-0877 Impact factor: 8.192