Prasad Durbaka V R, Richards Sabrina, Mai Xoi Muoi, Dong Chen
Department of Immunology, University of Washington School of Medicine, Seattle, WA 98195, USA.
Immunity. 2003 Jun;18(6):863-73. doi: 10.1016/s1074-7613(03)00147-x.
T cell activation by antigen-presenting cells (APC) is regulated by positive and negative costimulatory molecules in the B7 family. Here we describe a novel addition in this family, designated as B7S1, which is uniquely anchored to the cell membrane via a GPI linkage. B7S1 is expressed on professional APC and widely distributed in nonlymphoid tissues. A soluble B7S1-Ig fusion protein binds to activated but not naive T cells. B7S1-Ig inhibits T cell activation and IL-2 production. A monoclonal antibody that blocks binding of B7S1 to its receptor enhances T cell proliferation in vitro and exacerbates experimental autoimmune encephalomyelitis in vivo. This study identifies a novel negative regulator of T cell activation and further reveals complex costimulatory regulation of immune responses.
抗原呈递细胞(APC)对T细胞的激活受B7家族中正负共刺激分子的调控。在此,我们描述了该家族中的一个新成员,命名为B7S1,它通过糖基磷脂酰肌醇(GPI)连接独特地锚定在细胞膜上。B7S1在专职APC上表达,并广泛分布于非淋巴组织中。可溶性B7S1-Ig融合蛋白可与活化的而非未活化的T细胞结合。B7S1-Ig抑制T细胞激活和白细胞介素-2的产生。一种阻断B7S1与其受体结合的单克隆抗体在体外增强T细胞增殖,并在体内加剧实验性自身免疫性脑脊髓炎。本研究鉴定出一种新型的T细胞激活负调节因子,并进一步揭示了免疫反应复杂的共刺激调节机制。