CD38标记了肝细胞癌中已耗尽的CD8+组织内存T细胞
Marie J Y Reolo1, Masayuki Otsuka1, Justine Jia Wen Seow2
1Translational Immunology Institute (TII), SingHealth-DukeNUS Academic Medical Centre, Singapore, Singapore.
Frontiers in immunology
|June 28, 2023
概括
CD38是肝细胞癌 (HCC) 中T细胞耗尽的标志物. 它与CD8+T细胞上的耗尽标记的共同表达与HCC的攻击性相关,并表明了治疗点.
科学领域:
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
背景情况:
- 肝细胞癌 (HCC) 的免疫治疗显示出适度的反应率,需要对瘤微环境 (TME) 进行更深入的了解.
- CD38在HCC中的瘤透白细胞 (TILs) 上表达,但其具体作用尚不清楚.
研究的目的:
- 研究CD38在HCCTME中的作用及其与T细胞耗尽的相关性.
主要方法:
- 使用细胞计量飞行时间 (CyTOF),大量RNA测序,单细胞RNA (scRNA) 测序和多重免疫组织化学 (mIHC).
- 分析了来自HCC患者的TIL,非瘤透白细胞 (NIL) 和外周血液单核细胞 (PBMC) 中白细胞的CD38表达.
主要成果:
- 在HCC瘤中,CD38在CD8+ T居住记忆 (TRM) 细胞上高度表达.
- 在瘤透的CD8+ T细胞中观察到CD38与耗尽标记 (PDCD1,CTLA4,ITGAE) 的同时表达.
- 较高比例的CD38+PD-1+CD8+T细胞和TRM细胞与先进的HCC组织病理等级相关.
结论:
- CD38是T细胞耗尽的关键标志物,在HCC中起作用.
- CD38代表了一种潜在的治疗标,用于增强HCC中抗瘤细胞毒性T细胞的功能.
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