Mackay F, Woodcock S A, Lawton P, Ambrose C, Baetscher M, Schneider P, Tschopp J, Browning J L
Department of Immunology, Inflammation and Cell Biology, Biogen, Cambridge, Massachusetts 02142, USA.
J Exp Med. 1999 Dec 6;190(11):1697-710. doi: 10.1084/jem.190.11.1697.
The cause of many autoimmune and inflammatory diseases is unresolved, although dysregulated production of tumor necrosis factor (TNF) family members appears to be important in many cases. BAFF, a new member of the TNF family, binds to B cells and costimulates their growth in vitro. Mice transgenic for BAFF have vastly increased numbers of mature B and effector T cells, and develop autoimmune-like manifestations such as the presence of high levels of rheumatoid factors, circulating immune complexes, anti-DNA autoantibodies, and immunoglobulin deposition in the kidneys. This phenotype is reminiscent of certain human autoimmune disorders and suggests that dysregulation of BAFF expression may be a critical element in the chain of events leading to autoimmunity.
许多自身免疫性疾病和炎症性疾病的病因尚未明确,尽管肿瘤坏死因子(TNF)家族成员的产生失调在许多情况下似乎起着重要作用。BAFF是TNF家族的一个新成员,它与B细胞结合并在体外共刺激其生长。转BAFF基因的小鼠成熟B细胞和效应T细胞数量大幅增加,并出现自身免疫样表现,如类风湿因子水平升高、循环免疫复合物、抗DNA自身抗体以及肾脏中的免疫球蛋白沉积。这种表型让人联想到某些人类自身免疫性疾病,提示BAFF表达失调可能是导致自身免疫的一系列事件中的关键因素。