CD19
嵌合抗原受体
杂合子丢失
生物
抗原
癌症研究
突变
免疫学
基因
遗传学
T细胞
等位基因
免疫系统
作者
Elena J. Orlando,Xia Han,Catherine Tribouley,Patricia A. Wood,Rebecca Leary,Markus Riester,John E. Levine,Muna Qayed,Stephan A. Grupp,Michael Boyer,Barbara De Moerloose,Eneida R. Nemecek,Henrique Bittencourt,Hidefumi Hiramatsu,Jochen Buechner,Stella M. Davies,Michael R. Verneris,Kevin T. Nguyen,Jennifer L. Brogdon,Hans Bitter
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2018-09-27
卷期号:24 (10): 1504-1506
被引量:564
标识
DOI:10.1038/s41591-018-0146-z
摘要
We identified genetic mutations in CD19 and loss of heterozygosity at the time of CD19- relapse to chimeric antigen receptor (CAR) therapy. The mutations are present in the vast majority of resistant tumor cells and are predicted to lead to a truncated protein with a nonfunctional or absent transmembrane domain and consequently to a loss of surface antigen. This irreversible loss of CD19 advocates for an alternative targeting or combination CAR approach.
科研通智能强力驱动
Strongly Powered by AbleSci AI