嵌合抗原受体
T细胞
化学
免疫学
生物
细胞生物学
免疫系统
作者
Raymone Pajarillo,Luca Paruzzo,Alberto Carturan,Ositadimma Ugwuanyi,Griffin White,Puneeth Guruprasad,Hatcher J. Ballard,Ruchi P. Patel,Yunlin Zhang,Yong Gu Lee,Seok Jae Albert Hong,Gregory M. Dittami,Marco Ruella
出处
期刊:Cytotherapy
[Elsevier BV]
日期:2024-02-16
卷期号:26 (5): 506-511
标识
DOI:10.1016/j.jcyt.2024.01.007
摘要
The successful development of CD19-targeted chimeric antigen receptor (CAR) T-cell therapies has led to an exponential increase in the number of patients recieving treatment and the advancement of novel CAR T products. Therefore, there is a strong need to develop streamlined platforms that allow rapid, cost-effective, and accurate measurement of the key characteristics of CAR T cells during manufacturing (i.e., cell number, cell size, viability, and basic phenotype).
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