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通过定义因子诱导具有类似永生化和功能的 CAR T 细胞。

Induction of immortal-like and functional CAR T cells by defined factors.

机构信息

State Key Laboratory of Molecular Oncology, Beijing Key Laboratory for Immunological Research on Chronic Diseases, School of Medicine, Institute for Immunology, Tsinghua University, Beijing, China.

SXMU-Tsinghua Collaborative Innovation Center for Frontier Medicine , Taiyuan, China.

出版信息

J Exp Med. 2024 May 6;221(5). doi: 10.1084/jem.20232368. Epub 2024 Mar 26.

Abstract

Long-term antitumor efficacy of chimeric antigen receptor (CAR) T cells depends on their functional persistence in vivo. T cells with stem-like properties show better persistence, but factors conferring bona fide stemness to T cells remain to be determined. Here, we demonstrate the induction of CAR T cells into an immortal-like and functional state, termed TIF. The induction of CARTIF cells depends on the repression of two factors, BCOR and ZC3H12A, and requires antigen or CAR tonic signaling. Reprogrammed CARTIF cells possess almost infinite stemness, similar to induced pluripotent stem cells while retaining the functionality of mature T cells, resulting in superior antitumor effects. Following the elimination of target cells, CARTIF cells enter a metabolically dormant state, persisting in vivo with a saturable niche and providing memory protection. TIF represents a novel state of T cells with unprecedented stemness, which confers long-term functional persistence of CAR T cells in vivo and holds broad potential in T cell therapies.

摘要

嵌合抗原受体 (CAR) T 细胞的长期抗肿瘤疗效取决于其在体内的功能持久性。具有干细胞样特性的 T 细胞显示出更好的持久性,但赋予 T 细胞真正干性的因素仍有待确定。在这里,我们证明了诱导 CAR T 细胞进入一种类似于永生和功能性的状态,称为 TIF。CARTIF 细胞的诱导依赖于两个因子 BCOR 和 ZC3H12A 的抑制,并且需要抗原或 CAR 持续信号。重编程的 CARTIF 细胞具有几乎无限的干性,类似于诱导多能干细胞,同时保留成熟 T 细胞的功能,从而产生更好的抗肿瘤效果。在靶细胞被消除后,CARTIF 细胞进入代谢休眠状态,在体内以饱和的生态位持续存在,并提供记忆保护。TIF 代表了 T 细胞的一种新状态,具有前所未有的干性,赋予 CAR T 细胞在体内的长期功能持久性,并在 T 细胞治疗中具有广泛的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2360/10965394/163df3b76c98/JEM_20232368_GA.jpg

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