免疫疗法
外周血单个核细胞
免疫系统
周边公差
T细胞
免疫学
外围设备
生物
细胞
免疫检查点
效应器
癌症研究
医学
内科学
遗传学
体外
作者
Sara Valpione,Elena Galvani,Joshua Tweedy,Piyushkumar A. Mundra,Antonia Banyard,Philippa Middlehurst,Jeff Barry,Sarah Mills,Zena Salih,John Weightman,Avinash Gupta,Gabriela Gremel,Franziska Baenke,Nathalie Dhomen,Paul Lorigan,Richard Marais
出处
期刊:Nature cancer
[Nature Portfolio]
日期:2020-02-10
卷期号:1 (2): 210-221
被引量:194
标识
DOI:10.1038/s43018-019-0022-x
摘要
Our understanding of how checkpoint inhibitors (CPIs) affect T cell evolution is incomplete, limiting our ability to achieve full clinical benefit from these drugs. Here, we analyzed peripheral T cell populations after one cycle of CPI treatment and identified a dynamic awakening of the immune system, as revealed by T cell evolution in response to treatment. We sequenced T cell receptors in plasma cell-free DNA and peripheral blood mononuclear cells and performed phenotypic analysis of peripheral T cell subsets from patients with metastatic melanoma treated with CPIs. We found that early peripheral T cell turnover and T cell receptor repertoire dynamics identified which patients would respond to treatment. Additionally, the expansion of a subset of immune effector peripheral T cells we call TIE cells correlated with response. These events are prognostic and occur within 3 weeks of starting immunotherapy, raising the potential for monitoring patients’ responses by using minimally invasive liquid biopsies. Marais and colleagues report that checkpoint inhibitor treatment of patients with melanoma leads to dynamic changes in peripheral T cells and expansion of immune effector cells. This awakening of the immune system occurs early after treatment and could be exploited in the clinic.
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