B Cell-Activating Factor Belonging to the TNF Family (BAFF)-R Is the Principal BAFF Receptor Facilitating BAFF Costimulation of Circulating T and B Cells

Lai Guan Ng(Garvan Institute of Medical Research), Andrew P. R. Sutherland(Garvan Institute of Medical Research), Rebecca Newton(Garvan Institute of Medical Research), Fang Qian(Biogen (United States)), Teresa G. Cachero(Biogen (United States)), Martin Scott(Biogen (United States)), Jeffrey S. Thompson(Biogen (United States)), Julie Wheway(Garvan Institute of Medical Research), Tatyana Chtanova(Garvan Institute of Medical Research), Joanna R. Groom(Garvan Institute of Medical Research), Ian J Sutton(Garvan Institute of Medical Research), Cynthia Xin(Garvan Institute of Medical Research), Stuart G. Tangye(Centenary Institute), Susan L. Kalled(Biogen (United States)), Fabienne Mackay(Garvan Institute of Medical Research), Charles R. Mackay(Garvan Institute of Medical Research)
The Journal of Immunology
July 1, 2004
Cited by 494

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- micro 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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