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T 细胞 TET2 缺失解除抗肿瘤 CAR-T 细胞治疗的刹车

英文原题:T cell TET2 disruption cuts the breaks on antitumor CAR T cell therapy.

查看英文原题

T cell TET2 disruption cuts the breaks on antitumor CAR T cell therapy.

PubMed 2023/03/21(内容时间) Trends Immunol Q1 · IF 13.1(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T细胞要维持抗肿瘤应答,必须在体内保持功能性持续存留。近期Jain等人发现,在CAR-T 细胞中破坏TET2可导致抗原非依赖性CAR-T 细胞过度增殖,从而增强小鼠肿瘤控制;这一发现凸显了表观遗传策略改善T细胞癌症免疫疗法的潜力。

展开英文摘要原文

Functional persistence of chimeric antigen receptor (CAR) T cells is required for sustaining an antitumor response. Recently, Jain et al. revealed that disruption of TET2 in CAR T cells resulted in antigen-independent CAR T cell hyperproliferation that enhanced tumor control in mice, highlighting the potential of epigenetic strategies to improve T cell-based cancer immunotherapy.

论文信息

作者
Zebley CC、Youngblood B
第一作者单位
Department of Immunology, St Jude Children's Research Hospital, Memphis, TN 38105, USA; Department of Bone Marrow Transplantation and Cellular Therapy, St Jude Children's Research Hospital, Memphis, TN 38105, USA. Electronic address: Caitlin.Zebley@stjude.org.United States
通讯作者单位
Department of Immunology, St Jude Children's Research Hospital, Memphis, TN 38105, USA. Electronic address: Benjamin.Youngblood@stjude.org.United States
文献类型
非美国政府资助研究 · 美国 NIH 资助研究
期刊
Trends in immunology2023 Jun
原文标识
PubMed 36959018 · DOI 10.1016/j.it.2023.03.008