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肿瘤坏死因子/肿瘤坏死因子受体超家族成员在T细胞共刺激反应中的作用——再探讨

TNF/TNFR Superfamily Members in Costimulation of T Cell Responses-Revisited.

作者信息

Watts Tania H, Yeung Karen K M, Yu Tianning, Lee Seungwoo, Eshraghisamani Razieh

机构信息

Department of Immunology, University of Toronto, Toronto, Ontario, Canada; email:

出版信息

Annu Rev Immunol. 2025 Apr;43(1):113-142. doi: 10.1146/annurev-immunol-082423-040557. Epub 2025 Jan 2.

Abstract

Prosurvival tumor necrosis factor receptor (TNFR) superfamily (TNFRSF) members on T cells, including 4-1BB, CD27, GITR, and OX40, support T cell accumulation during clonal expansion, contributing to T cell memory. During viral infection, tumor necrosis factor superfamily (TNFSF) members on inflammatory monocyte-derived antigen-presenting cells (APCs) provide a postpriming signal (signal 4) for T cell accumulation, particularly in the tissues. Patients with loss-of-function mutations in TNFR/TNFSF members reveal a critical role for 4-1BB and CD27 in CD8 T cell control of Epstein-Barr virus and other childhood infections and of OX40 in CD4 T cell responses. Here, on the 20th anniversary of a previous article about TNFRSF signaling in T cells, we discuss the effects of endogenous TNFRSF signals in T cells upon recognition of TNFSF members on APCs; the role of TNFRSF members, including TNFR2, on regulatory T cells; and recent advances in the incorporation of TNFRSF signaling in T cells into immunotherapeutic strategies for cancer.

摘要

T细胞上的促生存肿瘤坏死因子受体(TNFR)超家族(TNFRSF)成员,包括4-1BB、CD27、糖皮质激素诱导的肿瘤坏死因子受体(GITR)和OX40,在克隆扩增过程中支持T细胞积累,有助于形成T细胞记忆。在病毒感染期间,炎症性单核细胞衍生的抗原呈递细胞(APC)上的肿瘤坏死因子超家族(TNFSF)成员为T细胞积累提供启动后信号(信号4),尤其是在组织中。TNFR/TNFSF成员功能丧失突变的患者显示,4-1BB和CD27在CD8 T细胞控制爱泼斯坦-巴尔病毒和其他儿童感染中起关键作用,而OX40在CD4 T细胞反应中起关键作用。在之前一篇关于T细胞中TNFRSF信号传导的文章发表20周年之际,我们讨论了T细胞中内源性TNFRSF信号在识别APC上的TNFSF成员时的作用;TNFRSF成员,包括TNFR2,在调节性T细胞上的作用;以及将T细胞中的TNFRSF信号传导纳入癌症免疫治疗策略的最新进展。

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