Sperling A I, Green J M, Mosley R L, Smith P L, DiPaolo R J, Klein J R, Bluestone J A, Thompson C B
Ben May Institute, University of Chicago, Chicago, Illinois 60637, USA.
J Exp Med. 1995 Jul 1;182(1):139-46. doi: 10.1084/jem.182.1.139.
Costimulation mediated by the CD28 receptor has been shown to play an important role in the development of a vigorous T cell immune response. Nevertheless, CD28-deficient mice can mount effective T cell-dependent immune responses. These data suggest that other costimulatory molecules may play a role in T cell activation. In a search for other costimulatory receptors on T cells, we have characterized a monoclonal antibody (mAb) that can costimulate T cells in the absence of accessory cells. Similar to CD28 antibodies, this mAb, R2/60, was found to synergize with T cell receptor engagement in inducing proliferation. Independent ligation of CD3 and the ligand recognized by R2/60 results in T cell proliferation, suggesting that the two molecules do not have to colocalize to activate the R2/60 costimulatory pathway. R2/60 does not react with CD28, and furthermore, R2/60 costimulates in a CD28-independent fashion since the mAb costimulates T cells from the CD28-deficient mice as well as wild-type mice. Expression cloning of the R2/60 antigen identified the ligand as murine CD43. Together, these data demonstrate that CD43 can serve as a receptor on T cells that can provide CD28-independent costimulation.
由CD28受体介导的共刺激已被证明在强大的T细胞免疫反应的发展中起重要作用。然而,缺乏CD28的小鼠仍能产生有效的T细胞依赖性免疫反应。这些数据表明其他共刺激分子可能在T细胞活化中发挥作用。为了寻找T细胞上的其他共刺激受体,我们鉴定了一种单克隆抗体(mAb),它可以在没有辅助细胞的情况下共刺激T细胞。与CD28抗体类似,这种mAb,即R2/60,被发现与T细胞受体结合协同诱导增殖。CD3和R2/60识别的配体的独立连接导致T细胞增殖,这表明这两种分子不必共定位以激活R2/60共刺激途径。R2/60不与CD28反应,此外,R2/60以不依赖CD28的方式共刺激,因为该mAb能共刺激来自缺乏CD28的小鼠以及野生型小鼠的T细胞。R2/60抗原的表达克隆确定该配体为小鼠CD43。总之,这些数据表明CD43可以作为T细胞上的一种受体,提供不依赖CD28的共刺激。