School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou 511442, China; National Engineering Research Center for Tissue Restoration and Reconstruction, South China University of Technology, Guangzhou 510006, China.
School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou International Campus, Guangzhou 511442, China; National Engineering Research Center for Tissue Restoration and Reconstruction, South China University of Technology, Guangzhou 510006, China; Guangdong Provincial Key Laboratory of Biomedical Engineering, South China University of Technology, Guangzhou 510006, China.
Sci Bull (Beijing). 2024 Feb 15;69(3):354-366. doi: 10.1016/j.scib.2023.11.055. Epub 2023 Dec 1.
Engineered T cells expressing chimeric antigen receptor (CAR) exhibit high response rates in B-cell malignancy treatments and possess therapeutic potentials against various diseases. However, the complicated ex vivo production process of CAR-T cells limits their application. Herein, we use virus-mimetic fusogenic nanovesicles (FuNVs) to produce CAR-T cells in vivo via membrane fusion-mediated CAR protein delivery. Briefly, the FuNVs are modified using T-cell fusogen, adapted from measles virus or reovirus fusogens via displaying anti-CD3 single-chain variable fragment. The FuNVs can efficiently fuse with the T-cell membrane in vivo, thereby delivering the loaded anti-CD19 (αCD19) CAR protein onto T-cells to produce αCD19 CAR-T cells. These αCD19 CAR-T cells alone or in combination with anti-OX40 antibodies can treat B-cell lymphoma without inducing cytokine release syndrome. Thus, our strategy provides a novel method for engineering T cells into CAR-T cells in vivo and can further be employed to deliver other therapeutic membrane proteins.
工程化表达嵌合抗原受体 (CAR) 的 T 细胞在 B 细胞恶性肿瘤治疗中表现出高反应率,并具有针对多种疾病的治疗潜力。然而,CAR-T 细胞的复杂体外生产过程限制了其应用。在此,我们使用病毒模拟融合纳米囊泡(FuNVs)通过膜融合介导的 CAR 蛋白递送来体内产生 CAR-T 细胞。简单来说,通过展示抗 CD3 单链可变片段,FuNVs 经过来自麻疹病毒或呼肠孤病毒融合蛋白的改造。FuNVs 可以在体内有效地与 T 细胞膜融合,从而将负载的抗 CD19(αCD19)CAR 蛋白递送到 T 细胞上,产生 αCD19 CAR-T 细胞。这些 αCD19 CAR-T 细胞单独或与抗 OX40 抗体联合使用可以治疗 B 细胞淋巴瘤而不会引起细胞因子释放综合征。因此,我们的策略为体内工程化 T 细胞成为 CAR-T 细胞提供了一种新方法,并且可以进一步用于递送电镜治疗蛋白。