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免疫疗法一个周期后外周 T 细胞动力学揭示的免疫唤醒。

Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy.

机构信息

Molecular Oncology Group, Cancer Research UK Manchester Institute, The University of Manchester, Alderley Park, UK.

The Christie NHS Foundation Trust, Manchester, UK.

出版信息

Nat Cancer. 2020 Feb;1(2):210-221. doi: 10.1038/s43018-019-0022-x. Epub 2020 Feb 10.

Abstract

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."

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/083e/7046489/6a3cc1480652/EMS85253-f008.jpg

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