Olivia Newton-John Cancer Research Institute and La Trobe University School of Cancer Medicine, Heidelberg, Victoria 3084, Australia.
Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia.
Sci Immunol. 2023 Oct 13;8(88):eadf2163. doi: 10.1126/sciimmunol.adf2163. Epub 2023 Oct 6.
Intraepithelial lymphocytes (IELs), including αβ and γδ T cells (T-IELs), constantly survey and play a critical role in maintaining the gastrointestinal epithelium. We show that cytotoxic molecules important for defense against cancer were highly expressed by T-IELs in the small intestine. In contrast, abundance of colonic T-IELs was dependent on the microbiome and displayed higher expression of TCF-1/ and a reduced effector and cytotoxic profile, including low expression of granzymes. Targeted deletion of TCF-1 in γδ T-IELs induced a distinct effector profile and reduced colon tumor formation in mice. In addition, TCF-1 expression was significantly reduced in γδ T-IELs present in human colorectal cancers (CRCs) compared with normal healthy colon, which strongly correlated with an enhanced γδ T-IEL effector phenotype and improved patient survival. Our work identifies TCF-1 as a colon-specific T-IEL transcriptional regulator that could inform new immunotherapy strategies to treat CRC.
上皮内淋巴细胞(IELs),包括αβ和γδ T 细胞(T-IELs),不断地对胃肠道上皮进行监测并发挥着关键作用。我们发现,在小肠中,T-IELs 高度表达了对抗癌症的重要细胞毒性分子。相比之下,结肠 T-IELs 的丰度依赖于微生物组,并表现出更高的 TCF-1 表达和降低的效应子和细胞毒性特征,包括颗粒酶的低表达。在 γδ T-IELs 中靶向敲除 TCF-1 会诱导出明显的效应子特征,并减少小鼠的结肠肿瘤形成。此外,与正常健康结肠相比,在人类结直肠癌(CRC)中存在的 γδ T-IELs 中 TCF-1 的表达显著降低,这与增强的 γδ T-IEL 效应子表型和改善患者生存密切相关。我们的工作确定了 TCF-1 是一种结肠特异性的 T-IEL 转录调节剂,它可以为治疗 CRC 的新免疫治疗策略提供信息。