McKenzie Brienne, Valitutti Salvatore
INSERM U1037, Centre de Recherche en Cancérologie de Toulouse (CRCT), Université de Toulouse III-Paul Sabatier, 31057 Toulouse, France.
INSERM U1037, Centre de Recherche en Cancérologie de Toulouse (CRCT), Université de Toulouse III-Paul Sabatier, 31057 Toulouse, France; Department of Pathology, Institut Universitaire du Cancer-Oncopole de Toulouse, 31059 Toulouse, France.
Trends Cancer. 2023 Mar;9(3):198-211. doi: 10.1016/j.trecan.2022.12.003. Epub 2022 Dec 31.
Cytotoxic T lymphocytes (CTLs) are antigen-specific killer cells equipped to identify and eliminate host cells that have been altered through infection or transformation. Both chimeric antigen-receptor (CAR) T cell therapies and immune checkpoint blockade (ICB) therapies are based on successful elimination of tumor cells by cytotoxic effectors. In this opinion article, we outline cell-intrinsic mechanisms by which tumor cells defend against CTLs, highlighting pathways that confer resistance and proposing opportunities for combination therapies. We discuss how exogenous killing entities [e.g., supramolecular attack particles (SMAPs)] offer a novel strategy to circumvent cellular resistance mechanisms. Our opinion article highlights the importance of identifying, quantifying, and targeting tumor defense mechanisms at the interface between tumor cells and CTLs as a critical consideration in the development of immunotherapy approaches.
细胞毒性T淋巴细胞(CTLs)是抗原特异性杀伤细胞,能够识别并清除因感染或转化而发生改变的宿主细胞。嵌合抗原受体(CAR)T细胞疗法和免疫检查点阻断(ICB)疗法均基于细胞毒性效应器成功消除肿瘤细胞。在这篇观点文章中,我们概述了肿瘤细胞抵御CTLs的细胞内在机制,重点介绍了赋予抗性的途径,并提出了联合治疗的机会。我们讨论了外源性杀伤实体[例如,超分子攻击颗粒(SMAPs)]如何提供一种规避细胞抗性机制的新策略。我们的观点文章强调了识别、量化和靶向肿瘤细胞与CTLs之间界面处的肿瘤防御机制的重要性,这是免疫治疗方法开发中的关键考虑因素。