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肾细胞癌浸润的 CD3 Vγ9Vδ1 T 细胞代表潜在的新型抗肿瘤免疫效应细胞。

Renal Cell Carcinoma-Infiltrating CD3 Vγ9Vδ1 T Cells Represent Potentially Novel Anti-Tumor Immune Players.

机构信息

Center for Urologic Cancer, National Cancer Center, Department of Urology, Goyang 10408, Korea.

Department of Immunology, Sungkyunkwan University School of Medicine, Suwon 16419, Korea.

出版信息

Curr Issues Mol Biol. 2021 May 27;43(1):226-239. doi: 10.3390/cimb43010019.

Abstract

Due to the highly immunogenic nature of renal cell carcinoma (RCC), the tumor microenvironment (TME) is enriched with various innate and adaptive immune subsets. In particular, gamma-delta (γδ) T cells can act as potent attractive mediators of adoptive cell transfer immunotherapy because of their unique properties such as non-reliance on major histocompatibility complex expression, their ability to infiltrate human tumors and recognize tumor antigens, relative insensitivity to immune checkpoint molecules, and broad tumor cytotoxicity. Therefore, it is now critical to better characterize human γδ T-cell subsets and their mechanisms in RCCs, especially the stage of differentiation. In this study, we aimed to identify γδ T cells that might have adaptive responses against RCC progression. We characterized γδ T cells in peripheral blood and tumor-infiltrating lymphocytes (TILs) in freshly resected tumor specimens from 20 RCC patients. Furthermore, we performed a gene set enrichment analysis on RNA-sequencing data from The Cancer Genome Atlas (TCGA) derived from normal kidneys and RCC tumors to ascertain the association between γδ T-cell infiltration and anti-cancer immune activity. Notably, RCC-infiltrating CD3 Vγ9Vδ1 T cells with a terminally differentiated effector memory phenotype with up-regulated activation/exhaustion molecules were newly detected as predominant TILs, and the cytotoxic activity of these cells against RCC was confirmed in vitro. In an additional analysis of the TCGA RCC dataset, γδ T-cell enrichment scores correlated strongly with those for CTLs, Th1 cells, "exhausted" T cells, and M1 macrophages, suggesting active involvement of γδ T cells in anti-tumor rather than pro-tumor activity, and Vδ1 cells were more abundant than Vδ2 or Vδ3 cells in RCC tumor samples. Thus, we posit that Vγ9Vδ1 T cells may represent an excellent candidate for adoptive immunotherapy in RCC patients with a high risk of relapse after surgery.

摘要

由于肾细胞癌 (RCC) 具有高度的免疫原性,肿瘤微环境 (TME) 富含各种先天和适应性免疫亚群。特别是 γδ (γδ) T 细胞因其独特的特性,如不依赖主要组织相容性复合体表达、能够浸润人体肿瘤并识别肿瘤抗原、对免疫检查点分子相对不敏感以及广泛的肿瘤细胞毒性,可作为过继细胞转移免疫治疗的有效吸引介质。因此,现在迫切需要更好地描述 RCC 中人类 γδ T 细胞亚群及其机制,尤其是分化阶段。在这项研究中,我们旨在鉴定可能对 RCC 进展具有适应性反应的 γδ T 细胞。我们对 20 名 RCC 患者的外周血和肿瘤浸润淋巴细胞 (TIL) 中的 γδ T 细胞进行了特征描述。此外,我们对来自癌症基因组图谱 (TCGA) 的正常肾脏和 RCC 肿瘤的 RNA 测序数据进行了基因集富集分析,以确定 γδ T 细胞浸润与抗癌免疫活性之间的关联。值得注意的是,新发现 RCC 浸润的 CD3 Vγ9Vδ1 T 细胞是具有终末分化效应记忆表型且上调激活/耗竭分子的主要 TIL,并且这些细胞对 RCC 的细胞毒性在体外得到了证实。在对 TCGA RCC 数据集的进一步分析中,γδ T 细胞富集评分与 CTL、Th1 细胞、“耗竭”T 细胞和 M1 巨噬细胞的评分密切相关,这表明 γδ T 细胞积极参与抗肿瘤而非促肿瘤活动,并且 Vδ1 细胞在 RCC 肿瘤样本中比 Vδ2 或 Vδ3 细胞更为丰富。因此,我们认为 Vγ9Vδ1 T 细胞可能是手术后复发风险高的 RCC 患者过继免疫治疗的一个很好的候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bb8/8929056/ddfa59d865d9/cimb-43-00019-g001.jpg

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