嵌合抗原受体
抗原
神经母细胞瘤
癌症研究
免疫系统
生物
细胞培养
细胞生物学
免疫学
T细胞
遗传学
作者
Sabine Heitzeneder,Kristopher R. Bosse,Zhongyu Zhu,Doncho V. Zhelev,Robbie G. Majzner,Molly Radosevich,Shaurya Dhingra,Elena Sotillo,Samantha N. Buongervino,Guillem Pascual‐Pasto,Emily Garrigan,Peng Xu,Jing Huang,Benjamin Salzer,Alberto Delaidelli,Swetha Raman,Hong Cui,Benjamin Martinez,Scott J. Bornheimer,Bita Sahaf
出处
期刊:Cancer Cell
[Cell Press]
日期:2021-12-30
卷期号:40 (1): 53-69.e9
被引量:121
标识
DOI:10.1016/j.ccell.2021.12.005
摘要
Pediatric cancers often mimic fetal tissues and express proteins normally silenced postnatally that could serve as immune targets. We developed T cells expressing chimeric antigen receptors (CARs) targeting glypican-2 (GPC2), a fetal antigen expressed on neuroblastoma (NB) and several other solid tumors. CARs engineered using standard designs control NBs with transgenic GPC2 overexpression, but not those expressing clinically relevant GPC2 site density (∼5,000 molecules/cell, range 1-6 × 10
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