微卫星不稳定性
无容量
彭布罗利珠单抗
肿瘤浸润淋巴细胞
免疫疗法
结直肠癌
医学
免疫检查点
癌症免疫疗法
DNA错配修复
易普利姆玛
癌症
免疫系统
黑色素瘤
癌症研究
肿瘤科
免疫学
内科学
生物
等位基因
基因
微卫星
生物化学
作者
Ziyi Bai,Yao Zhou,Zifan Ye,Jialong Xiong,Hongying Lan,Feng Wang
标识
DOI:10.3389/fimmu.2021.808964
摘要
The clinical success of immunotherapy has revolutionized the treatment of cancer patients, bringing renewed attention to tumor-infiltrating lymphocytes (TILs) of various cancer types. Immune checkpoint blockade is effective in patients with mismatched repair defects and high microsatellite instability (dMMR-MSI-H) in metastatic colorectal cancer (CRC), leading the FDA to accelerate the approval of two programmed cell death 1 (PD-1) blocking antibodies, pembrolizumab and nivolumab, for treatment of dMMR-MSI-H cancers. In contrast, patients with proficient mismatch repair and low levels of microsatellite stability or microsatellite instability (pMMR-MSI-L/MSS) typically have low tumor-infiltrating lymphocytes and have shown unsatisfied responses to the immune checkpoint inhibitor. Different TILs environments reflect different responses to immunotherapy, highlighting the complexity of the underlying tumor-immune interaction. Profiling of TILs fundamental Indication would shed light on the mechanisms of cancer-immune evasion, thus providing opportunities for the development of novel therapeutic strategies. In this review, we summarize phenotypic diversities of TILs and their connections with prognosis in CRC and provide insights into the subsets-specific nature of TILs with different MSI status. We also discuss current clinical immunotherapy approaches based on TILs as well as promising directions for future expansion, and highlight existing clinical data supporting its use.
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