Ni Ling, Dong Chen
Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.
Immunol Rev. 2017 Mar;276(1):52-65. doi: 10.1111/imr.12524.
Immune responses must be fine-tuned to allow effective clearance of invading pathogens, while maintain tolerance to self-antigens. T cells are the major effector cells for fighting and killing tumor cells. Immune checkpoints play a pivotal role in T cell activation, and determine the functional outcome of T cell receptor (TCR) signaling. The blockade of immune checkpoints CTLA-4 and PD-1 has already been one of the most successful cancer immunotherapies. In this review, we will focus on three novel inhibitory B7 family checkpoint molecules, B7-H3, B7S1 and VISTA. The aim of this article is to summarize their expressions in tumors as well as their roles in controlling and suppressing T cell immune responses and anti-tumor immunity. These pathways may be explored in future cancer immunotherapy.
免疫反应必须进行精细调节,以有效清除入侵病原体,同时维持对自身抗原的耐受性。T细胞是对抗和杀伤肿瘤细胞的主要效应细胞。免疫检查点在T细胞活化中起关键作用,并决定T细胞受体(TCR)信号传导的功能结果。免疫检查点CTLA-4和PD-1的阻断已经成为最成功的癌症免疫疗法之一。在本综述中,我们将聚焦于三种新型抑制性B7家族检查点分子,即B7-H3、B7S1和VISTA。本文旨在总结它们在肿瘤中的表达情况,以及它们在控制和抑制T细胞免疫反应及抗肿瘤免疫中的作用。这些途径可能会在未来的癌症免疫治疗中得到探索。