| Literature DB >> 26647406 |
Keishi Fujio1, Tomohisa Okamura2, Shuji Sumitomo3, Kazuhiko Yamamoto2.
Abstract
Autoreactive B cells play a crucial role in the pathogenesis of autoimmune diseases by producing auto-antibodies and presenting antigens. Regulatory cytokines that simultaneously suppress multiple pathways have the potential to control autoreactive B cells. The generally inhibitory cytokine IL-10 may have a stimulatory effect on human B-cell survival and antibody production. TGF-β family cytokines can decrease or increase antibody production and can suppress B-cell proliferation and differentiation. In contrast to TGF-β1, which induces extensive fibrosis, TGF-β3 and bone morphogenetic protein 6 (BMP-6)/BMP-7 induce non-scarring wound healing and counteract tissue fibrosis. Therefore, TGF-β3 and BMP-6/BMP-7 may be clinically applicable as therapeutic cytokines that target B cells. Recent progress in protein engineering may enable us to generate novel biologic therapies based on TGF-β family cytokines. © The Japanese Society for Immunology. 2015. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: B cell; BMP; TGF-beta; regulatory T cell
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Year: 2015 PMID: 26647406 PMCID: PMC4889880 DOI: 10.1093/intimm/dxv069
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823