Taraban Vadim Y, Rowley Tania F, Al-Shamkhani Aymen
Cancer Sciences Division, Tenovus Research Laboratory, University of Southampton School of Medicine, Southampton General Hospital, Southampton, United Kingdom.
J Immunol. 2004 Dec 1;173(11):6542-6. doi: 10.4049/jimmunol.173.11.6542.
The CD154/CD40 interaction is an important pathway of CD4 T cell help for CD8 T cell responses. In this study, we address the role of CD70, a member of the TNF superfamily and the ligand for the T cell costimulatory receptor CD27, in CD40-mediated priming of CD8 T cells. Using an agonistic anti-CD40 mAb to mimic the CD154/CD40 interaction we demonstrate that the priming of OT-I TCR transgenic or endogenous mouse OVA-specific CD8 T cells is critically dependent on CD70/CD27 interaction. CD70 blockade inhibited CD40-mediated clonal expansion of CD8 T cells and reduced the number of memory CD8 T cells generated. Furthermore, CD70 blockade during the initial priming of CD8 T cells inhibited the ability of memory CD8 T cells to expand in response to a second encounter with Ag. Our data indicate that CD70 expression on APCs plays a key role in CD40-dependent CD8 T cell responses.
CD154/CD40相互作用是CD4 T细胞辅助CD8 T细胞应答的重要途径。在本研究中,我们探讨了肿瘤坏死因子超家族成员、T细胞共刺激受体CD27的配体CD70在CD40介导的CD8 T细胞致敏中的作用。使用激动性抗CD40单克隆抗体模拟CD154/CD40相互作用,我们证明OT-I TCR转基因或内源性小鼠OVA特异性CD8 T细胞的致敏关键依赖于CD70/CD27相互作用。CD70阻断抑制了CD40介导的CD8 T细胞克隆扩增,并减少了产生的记忆CD8 T细胞数量。此外,在CD8 T细胞初始致敏期间进行CD70阻断,抑制了记忆CD8 T细胞在再次接触抗原时的扩增能力。我们的数据表明,抗原呈递细胞上的CD70表达在CD40依赖性CD8 T细胞应答中起关键作用。