PD-1-mediated inhibition of T cell activation: Mechanisms and strategies for cancer combination immunotherapy

Rui Liu , Hui-Fang Li , Shu Li
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引用次数: 0

Abstract

The programmed cell death 1 (PD-1) immune checkpoint of co-inhibitory signaling plays crucial roles in controlling the magnitude and duration of T cell activation to limit tissue damage and maintain self-tolerance. Cancer cells hijack the co-inhibitory pathway and escape immune surveillance by overexpressing the PD-1 ligand PD-L1. Immune checkpoint inhibitors, such as PD-1 blocking antibody have been approved for tumor immunotherapy. However, not all patients can benefit from PD-1 monotherapy. Combination immunotherapy based on PD-1 axis blockade substantially improves clinical anti-tumor efficacy. In this review, we briefly summarize the current progress on the mechanisms of PD-1-mediated inhibition of T cell activation and strategies for cancer combination immunotherapy.

PD-1 介导的 T 细胞活化抑制:癌症联合免疫疗法的机制与策略
协同抑制信号的程序性细胞死亡 1(PD-1)免疫检查点在控制 T 细胞活化的程度和持续时间以限制组织损伤和维持自我耐受方面发挥着至关重要的作用。癌细胞通过过度表达 PD-1 配体 PD-L1 来劫持协同抑制通路并逃避免疫监视。免疫检查点抑制剂(如 PD-1 阻断抗体)已被批准用于肿瘤免疫疗法。然而,并非所有患者都能从 PD-1 单药治疗中获益。基于PD-1轴阻断的联合免疫疗法可大幅提高临床抗肿瘤疗效。在这篇综述中,我们简要总结了 PD-1 介导的 T 细胞活化抑制机制和肿瘤联合免疫疗法策略的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell insight
Cell insight Neuroscience (General), Biochemistry, Genetics and Molecular Biology (General), Cancer Research, Cell Biology
CiteScore
2.70
自引率
0.00%
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0
审稿时长
35 days
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