CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Resisting T cell attack: tumor-cell-intrinsic defense and reparation mechanisms.
Resisting T cell attack: tumor-cell-intrinsic defense and reparation mechanisms.
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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细胞成功清除肿瘤细胞。在这篇观点文章中,我们概述了肿瘤细胞防御CTLs的细胞内在机制,重点阐述了赋予耐药性的通路,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)]如何提供一种新策略来规避细胞耐药机制。我们的观点文章强调,识别、量化和靶向肿瘤细胞与CTLs界面处的肿瘤防御机制,是免疫治疗方法开发中的关键考量。
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.
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