决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Bispecific killer cell engager-secreting CAR-T cells redirect natural killer specificity to enhance antitumour responses.
这些研究结果表明,将分泌 BiKE 的 CAR-T 细胞与 NK 细胞联合使用,是对抗肿瘤抗原异质性和免疫逃逸的一种有前景的策略。
T细胞和自然杀伤(NK)细胞协同维持免疫稳态。当前的癌症免疫疗法主要依赖这些细胞的单独应用。本研究利用双顺反子载体共表达嵌合抗原受体(CAR)和分泌型免疫细胞衔接器(ICE),充分发挥两种效应细胞类型的联合治疗潜力。在体外验证免疫细胞衔接器的分泌和功能后,在小鼠模型中系统比较了多种联合方案,确定了分泌双特异性杀伤细胞衔接器(BiKE)的CAR-T细胞与NK细胞的高效联合方案。与传统CAR-T细胞和NK细胞的简单联合相比,该策略在CD19 + B细胞白血病和淋巴瘤以及EGFR + 实体瘤模型中展现出更优的疗效,同时降低了对CAR-T细胞剂量的依赖。此外,靶向不同抗原的CAR-T细胞和BiKE能够抑制具有异质性抗原表达的肿瘤细胞。这些发现表明,将分泌BiKE的CAR-T细胞与NK细胞联合,为对抗肿瘤抗原异质性和免疫逃逸提供了一种有前景的策略。
T cells and natural killer (NK) cells collaborate to maintain immune homeostasis. Current cancer immunotherapies predominantly rely on the individual application of these cells. Here we use bicistronic vectors to co-express chimeric antigen receptors (CARs) and secreted immune cell engagers (ICEs), leveraging the combined therapeutic potential of both effector cell types. After in vitro validation of immune cell engager secretion and function, various combinatorial approaches are systematically compared in mouse models, identifying a highly effective combination of bispecific killer cell engager (BiKE)-secreting CAR-T cells and NK cells. Beyond a simple combination of conventional CAR-T cells and NK cells, this strategy demonstrates superior efficacy in CD19 + B cell leukaemia and lymphoma and EGFR + solid tumour models while reducing the dosage dependence on CAR-T cells. Moreover, CAR-T cells and BiKEs targeting distinct antigens exhibit suppression of tumour cells with heterogeneous antigen expression. These findings indicate that combining BiKE-secreting CAR-T cells and NK cells offers a promising strategy to combat tumour antigen heterogeneity and immune evasion.
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