B细胞激活因子
肿瘤坏死因子α
免疫学
B细胞
医学
抗体
作者
Lai Guan Ng,Andrew P. R. Sutherland,Rebecca Newton,Fang Qian,Teresa G. Cachero,Martin Scott,Jeffrey S. Thompson,Julie Wheway,Tatyana Chtanova,Joanna R. Groom,Ian Sutton,Cynthia Xin,Stuart G. Tangye,Susan L. Kalled,Fabienne Mackay,Charles R. Mackay
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2004-07-15
卷期号:173 (2): 807-817
被引量:489
标识
DOI:10.4049/jimmunol.173.2.807
摘要
Abstract BAFF (B cell-activating factor belonging to the TNF family) is a cell survival and maturation factor for B cells, and overproduction of BAFF is associated with systemic autoimmune disease. BAFF binds to three receptors, BAFF-R, transmembrane activator and calcium modulator and cyclophilin ligand interactor (TACI), and B cell maturation Ag (BCMA). Using specific mAbs, BAFF-R was found to be the predominant BAFF receptor expressed on peripheral B cells, in both humans and mice, and antagonist mAbs to BAFF-R blocked BAFF-mediated costimulation of anti-μ responses. The other BAFF receptors showed a much more restricted expression pattern, suggestive of specialized roles. BCMA was expressed by germinal center B cells, while TACI was expressed predominantly by splenic transitional type 2 and marginal zone B cells, as well as activated B cells, but was notably absent from germinal center B cells. BAFF was also an effective costimulator for T cells, and this costimulation occurs entirely through BAFF-R. BAFF-R, but not TACI or BCMA, was expressed on activated/memory subsets of T cells, and T cells from BAFF-R mutant A/WySnJ mice failed to respond to BAFF costimulation. Thus, BAFF-R is important not only for splenic B cell maturation, but is the major mediator of BAFF-dependent costimulatory responses in peripheral B and T cells.
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