嵌合抗原受体
细胞生物学
生物
干细胞
嵌合体(遗传学)
心理压抑
免疫学
T细胞
遗传学
免疫系统
基因
基因表达
作者
Lixia Wang,Gang Jin,Qiuping Zhou,Yanyan Liu,Xiaocui Zhao,Zhuoyang Li,Na Yin,Min Peng
标识
DOI:10.1101/2023.11.06.565785
摘要
Abstract Long-term antitumor efficacy of chimeric antigen receptor (CAR)-T cells depends on their functional persistence in vivo. T cells with stem-like property show better persistence, but factors conferring T cells bona fide stemness 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 CAR-TIF cells depends on repression of two factors: BCOR and ZC3H12A, and requires antigen or CAR tonic signaling. The reprogrammed CAR-TIF cells possess almost infinite stemness resembling induced pluripotent stem cells but retain functionality of mature T cells, which exhibit superior antitumor effect. CAR-TIF cells enter a metabolically dormant state after elimination of target cells, which persist in vivo with a saturable niche and mediate memory protection. CAR-TIF cells represent a novel state of T cells with unprecedented stemness conferring long-term functional persistence of CAR-T cells in vivo, which have broad potentials in T cell therapies.
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