B细胞激活因子
免疫学
免疫系统
B细胞
T细胞
细胞生物学
肿瘤坏死因子α
启动(农业)
生物
关节炎
抗体
植物
发芽
作者
Hua Wang,Scot A. Marsters,Thad Baker,Betty S. Chan,Wyne P. Lee,Ling Fu,Daniel B. Tumas,Minhong Yan,Vishva M. Dixit,Avi Ashkenazi,Iqbal S. Grewal
摘要
Interactions of the tumor necrosis factor superfamily members B lymphocyte stimulator (BLyS) and a proliferation-inducing ligand (APRIL) with their receptors-transmembrane activator and CAML interactor (TACI) and B cell maturation molecule (BCMA)-on B cells play an important role in the humoral immune response. Whereas BCMA is restricted to B cells, TACI is also expressed on activated T cells; we show here that TACI-Fc blocks the activation of T cells in vitro and inhibits antigen-specific T cell activation and priming in vivo. In a mouse model for rheumatoid arthritis (RA), an autoimmune disease that involves both B and T cell components, TACI-Fc treatment substantially inhibited inflammation, bone and cartilage destruction and disease development. Thus, BLyS and/or APRIL are important not only for B cell function but for T cell-mediated immune responses. Inhibition of these ligands might have therapeutic benefits for autoimmune diseases, such as RA, that involve both B and T cells.
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