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细胞膜片将 CAR 分子从细胞储库转移至常规 T 细胞以构建无需基因修饰的新型融合 CAR-T 细胞

英文原题:Cell membrane patches transfer CAR molecules from a cellular depot to conventional T cells for constructing innovative fused-CAR-T cells without necessitating genetic modification.

查看英文原题

Cell membrane patches transfer CAR molecules from a cellular depot to conventional T cells for constructing innovative fused-CAR-T cells without necessitating genetic modification.

PubMed 2024/08/05(内容时间) Exp Hematol Oncol Q1 · IF 17.5(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)是CAR-T 细胞的核心组成。外源CAR分子可在异体T细胞上产生功能作用,促使其活化并发生后续功能改变。本文基于这一生物学原理提出一种新方法:将外源细胞的CAR分子转移至受体T细胞膜上。该过程使受体T细胞能够识别靶抗原并被激活。这些膜片段赋予正常T细胞更强的肿瘤靶向能力,并激活其固有杀伤功能。该方法的效果提出了一种制备非基因改造CAR-T 细胞的途径,也可能适用于其他免疫细胞。

展开英文摘要原文

Chimeric antigen receptor (CAR) serves as the foundational element of CAR-T cells. Exogenous CAR molecules can exert functional effects on allogeneic T cells, leading to their activation and subsequent functional alterations.

Here we show a new method based on this biological principle: the transfer of CAR molecules from exogenous cells to the membrane of receptor T cells. This process facilitates receptor T cell to recognize target antigens and induces their activation. These patches imbued normal T cells with enhanced tumor targeting capabilities and activated their inherent killing functions. This method's efficacy introduces an approach for constructing non-genetically manipulated CAR-T cells and holds potential for application to other immune cells.

论文信息

作者
Hu J、Zhong L、Wang Y、Hu S、Zhang L、Tian Q
第一作者单位
School of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, 311121, China.China
通讯作者单位
School of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, 311121, China. tianqc@hznu.edu.cn.China
文献类型
读者来信
期刊
Experimental hematology & oncology2024 Aug 5
原文标识
PubMed 39103961 · DOI 10.1186/s40164-024-00545-z