Molecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.
The Christie NHS Foundation Trust, Manchester, UK.
Nat Cancer. 2020 Feb;1(2):210-221. doi: 10.1038/s43018-019-0022-x. Epub 2020 Feb 10.
Our understanding of how checkpoint inhibitors (CPI) 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 and identified a dynamic awakening of the immune system revealed by T cell evolution in response to treatment. We sequenced T cell receptors (TCR) in plasma cell-free DNA (cfDNA) and peripheral blood mononuclear cells (PBMC) and performed phenotypic analysis of peripheral T cell subsets from metastatic melanoma patients treated with CPI. We found that early peripheral T cell turnover and TCR repertoire dynamics identified which patients would respond to treatment. Additionally, the expansion of a subset of immune-effector peripheral T cells we call T cells correlated with response. These events are prognostic and occur within 3 weeks of starting immunotherapy, raising the potential for monitoring patients responses using minimally invasive liquid biopsies."
我们对于检查点抑制剂(CPI)如何影响 T 细胞进化的理解并不完整,这限制了我们从这些药物中获得完全临床获益的能力。在这里,我们分析了一个 CPI 治疗周期后的外周 T 细胞群,并通过 T 细胞对治疗的反应性进化,鉴定了一个由免疫系统动态唤醒所揭示的现象。我们对来自转移性黑色素瘤患者的外周血单个核细胞(PBMC)和血浆无细胞 DNA(cfDNA)中的 T 细胞受体(TCR)进行了测序,并对外周 T 细胞亚群进行了表型分析。我们发现,早期外周 T 细胞的更替和 TCR 库动力学可以识别出哪些患者对治疗有反应。此外,我们称之为 T 细胞的免疫效应器外周 T 细胞亚群的扩增与反应相关。这些事件具有预后意义,并发生在免疫治疗开始后的 3 周内,这为使用微创液体活检监测患者的反应提供了可能性。