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异体 CAR-T 细胞:复杂细胞治疗设计考验临床前模型的极限

英文原题:Allogeneic CAR T Cells: Complex Cellular Therapy Designs Test the Limits of Our Preclinical Models.

查看英文原题

Allogeneic CAR T Cells: Complex Cellular Therapy Designs Test the Limits of Our Preclinical Models.

PubMed 2024/04/02(内容时间) Cancer Immunol Res Q1 · IF 7.9(JCR 2025)

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中文摘要

目前所有获FDA批准的嵌合抗原受体(CAR)T细胞产品均为自体产品,这为广泛应用带来了若干挑战。本期中,Degagn及其同事报告了一项关于开发多发性骨髓瘤现货型CAR-T 细胞的临床前研究。他们利用CRISPR/Cas12a基因组编辑平台和基因敲入技术,消除同种异体反应性并降低细胞被自然杀伤(NK)细胞清除的易感性。该研究促成了一项正在开展的现货型CAR-T 细胞治疗多发性骨髓瘤I期临床试验。相关研究见Degagn等,第462页(2)。

展开英文摘要原文

All chimeric antigen receptor (CAR) T-cell products currently approved by the FDA are autologous, which poses several challenges for widespread use. In this issue, Degagn and colleagues present their preclinical research on creating off-the-shelf CAR T cells for multiple myeloma.

They utilized the CRISPR/Cas12a genome editing platform and gene knock-in techniques to eliminate alloreactivity and decrease susceptibility to natural killer (NK)-cell elimination. This work has led to an ongoing phase I trial of off-the-shelf CAR T cells for multiple myeloma treatment. See related article by Degagn et al. , p. 462 (2).

论文信息

作者
Caimi PF、Melenhorst JJ
第一作者单位
Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio.United States
通讯作者单位
Cleveland Clinic Lerner College of Medicine, Cleveland, Ohio.United States
文献类型
评论
期刊
Cancer immunology research2024 Apr 2
原文标识
PubMed 38562081 · DOI 10.1158/2326-6066.CIR-24-0204