嵌合抗原受体
肿瘤微环境
免疫系统
T细胞
癌细胞
抗原
细胞毒性T细胞
癌症疫苗
彭布罗利珠单抗
黑色素瘤
癌症治疗
作者
Yayi He,Jie Cao,Chao Zhao,Xuefei Li,Caicun Zhou,Fred R. Hirsch
摘要
Patients with malignant tumor treated with immunotherapy have received significant clinical benefits over the years. Immune checkpoint blocking agents, such as anti-cytotoxic T-lymphocyte-associated protein-4 (anti-CTLA-4) and anti-programmed cell death protein-1 (anti-PD-1) monoclonal antibodies, have produced impressive clinical results in different types of cancer. T-cell immunoglobulin and mucin domain-3 (TIM-3), another immune checkpoint, could inhibit cancer immunity. Recent studies have highlighted that TIM-3 has an important role to play in T-cell exhaustion and correlates with the outcome of anti-PD-1 therapy. Targeting TIM-3 might be a promising approach for cancer immunotherapy. Here, we review the role of TIM-3 in cancer and clinical trials with TIM-3 inhibitors.
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