Therapeutic potential of regulatory cytokines that target B cells

被引:7
|
作者
Fujio, Keishi [1 ]
Okamura, Tomohisa [1 ,2 ]
Sumitomo, Shuji [1 ]
Yamamoto, Kazuhiko [1 ,2 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Allergy & Rheumatol, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138655, Japan
[2] Univ Tokyo, Ctr Integrat Inflammol, Max Planck Univ Tokyo, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
关键词
B cell; BMP; regulatory T cell; TGF-beta; GROWTH-FACTOR-BETA; SYSTEMIC-LUPUS-ERYTHEMATOSUS; BONE MORPHOGENETIC PROTEINS; TGF-BETA; T-CELLS; TRANSCRIPTION FACTOR; MONOCLONAL-ANTIBODY; IG PRODUCTION; DOUBLE-BLIND; INDUCTION;
D O I
10.1093/intimm/dxv069
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory cytokines that target B cells.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-beta family cytokines can decrease or increase antibody production and can suppress B-cell proliferation and differentiation. In contrast to TGF-beta 1, which induces extensive fibrosis, TGF-beta 3 and bone morphogenetic protein 6 (BMP-6)/BMP-7 induce non-scarring wound healing and counteract tissue fibrosis. Therefore, TGF-beta 3 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-beta family cytokines.
引用
收藏
页码:189 / 195
页数:7
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