嵌合抗原受体
CD19
汽车T细胞治疗
细胞
细胞疗法
T细胞
B细胞
癌症研究
医学
免疫学
抗原
化学
免疫系统
抗体
生物化学
作者
Gregory M. Chen,J. Joseph Melenhorst,Kai Tan
出处
期刊:Science Translational Medicine
[American Association for the Advancement of Science (AAAS)]
日期:2022-06-22
卷期号:14 (650)
被引量:4
标识
DOI:10.1126/scitranslmed.abn3353
摘要
Chimeric antigen receptor (CAR) T cell therapies targeting CD19 and CD22 have been successful for treating B cell cancers, but CAR T cells targeting non-B cell cancers remain unsuccessful. We propose that rather than being strictly a side effect of therapy, the large number of CAR interactions with normal B cells may be a key contributor to clinical CAR T cell responses.
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