Anderson D E, Sharpe A H, Hafler D A
University of California (Davis) School of Medicine 95616, USA.
Curr Opin Immunol. 1999 Dec;11(6):677-83. doi: 10.1016/s0952-7915(99)00036-9.
The past year has seen significant advances in our understanding of the role of the B7-CD28/CTLA-4 pathway in regulating the responses of self-reactive T cells, giving impetus to manipulation of this pathway for treating human autoimmune diseases. Recent studies have demonstrated that B7-CD28 costimulation has critical roles in stimulating both the initiation and effector phases of autoimmunity and that CD28 regulates the threshold for activation of self-reactive T cells. Recent work has also revealed critical roles for CTLA-4 in limiting the extent of Th1/Th2 cell differentiation and in downregulating the responses of self-reactive T cells during both the initiation and progression of autoimmune disease.
在过去的一年里,我们对B7-CD28/CTLA-4通路在调节自身反应性T细胞应答中的作用有了重大进展,这推动了通过操纵该通路来治疗人类自身免疫性疾病。最近的研究表明,B7-CD28共刺激在刺激自身免疫的起始阶段和效应阶段均起关键作用,且CD28调节自身反应性T细胞的激活阈值。最近的研究还揭示了CTLA-4在限制Th1/Th2细胞分化程度以及在自身免疫性疾病的起始和进展过程中下调自身反应性T细胞应答方面的关键作用。