嵌合抗原受体
抗原
CD19
流式细胞术
多路复用
贪婪
染色
T细胞受体
T细胞
生物
化学
免疫学
分子生物学
免疫系统
生物信息学
遗传学
作者
Yifei Hu,Guoshuai Cao,Xiufen Chen,Xiaodan Huang,Nicholas Asby,Nicholas Ankenbruck,Ali Rahman,Ashima Thusu,Yonghui He,Peter A. Riedell,Michael Bishop,Hans Schreiber,Justin Kline,Jun Huang
出处
期刊:Matter
[Elsevier BV]
日期:2021-12-01
卷期号:4 (12): 3917-3940
被引量:5
标识
DOI:10.1016/j.matt.2021.09.027
摘要
Although chimeric antigen receptor (CAR) T cell therapy has transformed cancer treatment, high-quality and universal CAR-staining reagents are urgently required to manufacture CAR T cells, predict therapy response, decipher CAR biology, and engineer new CARs. Here, we developed tetrameric and dodecameric forms of a multifunctional and extensible category of high-avidity CAR-staining reagents: antigen multimers. Antigen multimers detected CARs against CD19, HER2, and Tn-glycoside with significantly higher specificity, sensitivity, and precision than existing reagents. In addition to accurate CAR T cell detection by flow cytometry, antigen multimers also enabled ≥100-fold magnetic enrichment of rare CAR T cells, selective CAR T cell stimulation, and high-dimensional CAR T cell profiling by single-cell multi-omics analyses. Finally, antigen multimers accurately captured clinical anti-CD19 CAR T cells from patients' cellular infusion products, post-infusion peripheral blood, and tumor biopsies. Antigen multimers can be readily extended to other CAR systems by switching the antigen ligand. As such, antigen multimers have broad clinical and research applications.
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