生物
结肠炎
封锁
细胞毒性T细胞
CD8型
癌症研究
免疫检查点
免疫疗法
趋化因子
炎症
T细胞
免疫系统
T细胞受体
癌症免疫疗法
受体
免疫学
体外
生物化学
作者
Adrienne Luoma,Shengbao Suo,Hannah L. Williams,Tatyana Sharova,Keri M. Sullivan,Michael P. Manos,Peter Bowling,F. Stephen Hodi,Osama E. Rahma,Ryan J. Sullivan,Genevieve M. Boland,Jonathan A. Nowak,Stephanie K. Dougan,Michael Dougan,Guo‐Cheng Yuan,Kai W. Wucherpfennig
出处
期刊:Cell
[Elsevier]
日期:2020-08-01
卷期号:182 (3): 655-671.e22
被引量:317
标识
DOI:10.1016/j.cell.2020.06.001
摘要
Checkpoint blockade with antibodies specific for the PD-1 and CTLA-4 inhibitory receptors can induce durable responses in a wide range of human cancers. However, the immunological mechanisms responsible for severe inflammatory side effects remain poorly understood. Here we report a comprehensive single-cell analysis of immune cell populations in colitis, a common and severe side effect of checkpoint blockade. We observed a striking accumulation of CD8 T cells with highly cytotoxic and proliferative states and no evidence of regulatory T cell depletion. T cell receptor (TCR) sequence analysis demonstrated that a substantial fraction of colitis-associated CD8 T cells originated from tissue-resident populations, explaining the frequently early onset of colitis symptoms following treatment initiation. Our analysis also identified cytokines, chemokines, and surface receptors that could serve as therapeutic targets for colitis and potentially other inflammatory side effects of checkpoint blockade.
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