共表达细胞因子和趋化因子的CAR-T细胞能更好地克服实体肿瘤的抑制微环境

V. Golubovskaya
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引用次数: 0

摘要

Keishi Adachi等人在《自然生物技术》杂志上发表的信函报告。March 5, 2018描述了一种结合CD20-CAR-T细胞共表达IL-7和CCL19的优雅方法,称为(7 × 19 CAR-T细胞)[4](图1)。IL-7和CCL19都是支持淋巴结和淋巴样组织中T细胞存活的关键因素。在实体瘤异种移植小鼠模型中,这些CD20 CAR-T细胞的存活率为100%,而标准或常规CAR-T细胞的存活率较低。在CAR构建体[1]内设计CD28或41-BB共刺激结构域时,7x19 CAR- t细胞的抗肿瘤作用相同。此外,与标准CAR-T细胞相比,这些CAR-T细胞表达的LAG-3、TIM-3、PD-1和其他检查点抑制剂水平显著降低,这表明它们的耗竭表型较少。此外,7x19 CAR-T细胞具有增强的迁移和增强的记忆功能,这是CAR-T细胞增强疗效的关键功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CAR-T cells with co-expressed cytokines and chemokines better overcome inhibitory microenvironment of solid tumors
The Letter report to Nature Biotechnology by Keishi Adachi, et al. March 5, 2018 describes an elegant approach to combine CD20-CAR-T cells that co-express IL-7 and CCL19, called (7 × 19 CAR-T cells) [4] (Figure 1). Both IL-7 and CCL19 are critical factors to support survival of T cells in lymph nodes and lymphoid tissues. In solid tumor xenograft mice mode, these CD20 CAR-T cells had 100% survival compared with lower survival of standard or conventional CAR-T cells. The anti-tumor effect of 7x19 CAR-T cells was the same when CD28 or 41-BB co-stimulatory domains were designed inside CAR construct [1]. In addition, these CAR-T cells expressed significantly lower levels of LAG-3, TIM-3, PD-1 and other checkpoint inhibitors compared with standard CAR-T cells which demonstrates their less exhausted phenotype. In addition, 7x19 CAR-T cells had increased migratory and increased memory functions that are key functions for increased efficacy of CAR-T cells.
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