CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:RevCAR-mediated T-cell response against PD-L1-expressing cells turns suppression into activation.
RevCAR-mediated T-cell response against PD-L1-expressing cells turns suppression into activation.
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将CAR-T 细胞疗法应用于实体瘤治疗尤为困难,原因在于免疫抑制性肿瘤微环境(TME)。尽管我们的模块化RevCAR系统增强了CAR-T 细胞疗法的安全性和可控性,但有效靶向实体瘤仍具挑战性。由于PD-L1是癌细胞及其微环境中常上调的免疫检查点,它是实体瘤的相关靶点。在此,我们引入一种新型PD-L1 RevTM,能够重定向RevCAR T细胞以特异性靶向并杀死表达PD-L1的肿瘤细胞,使其被激活并分泌促炎细胞因子。这在体外通过单层和3D模型(包括患者来源的培养物)以及体内实验中得到证实。此外,我们在体外和体内展示了通过Dual RevCAR系统对同时表达PD-L1和另一种肿瘤相关抗原的细胞进行AND门控靶向。我们的发现表明,RevCAR介导的PD-L1靶向可能是调节TME和改善实体瘤治疗的一种有前景的治疗策略。
Applying CAR T-cell therapy to treat solid tumors is especially challenging due to the immunosuppressive tumor microenvironment (TME). While our modular RevCAR system enhances the safety and controllability of CAR T-cell therapy, effectively targeting solid tumors remains difficult. Since PD-L1 is an immune checkpoint frequently upregulated by cancer cells and their microenvironment, it is a relevant target for solid tumors.
Here, we introduce a novel PD-L1 RevTM capable of redirecting RevCAR T-cells to specifically target and kill PD-L1-expressing tumor cells, becoming activated and secreting pro-inflammatory cytokines. This is shown in vitro with monolayer and 3D models, including patient-derived cultures, and in vivo.
Furthermore, we demonstrate in vitro and in vivo an AND-gated targeting of cells simultaneously expressing PD-L1 and another tumor-associated antigen by the Dual RevCAR system.
Our findings suggest that RevCAR-mediated targeting of PD-L1 could be a promising therapeutic approach for modulating the TME and improving solid tumor treatment.
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