嵌合抗原受体
食品药品监督管理局
医学
临床试验
CD19
细胞疗法
人口
抗原
免疫学
T细胞
生物
细胞
药理学
内科学
免疫系统
环境卫生
遗传学
作者
Claire Roddie,Maeve O’Reilly,Juliana Dias Alves Pinto,Ketki Vispute,Mark W. Lowdell
出处
期刊:Cytotherapy
[Elsevier]
日期:2019-03-01
卷期号:21 (3): 327-340
被引量:106
标识
DOI:10.1016/j.jcyt.2018.11.009
摘要
Clinical trials of adoptively transferred CD19 chimeric antigen receptor (CAR) T cells have delivered unprecedented responses in patients with relapsed refractory B-cell malignancy. These results have prompted Food and Drug Administration (FDA) approval of two CAR T-cell products in this high-risk patient population. The widening range of indications for CAR T-cell therapy and increasing patient numbers present a significant logistical challenge to manufacturers aiming for reproducible delivery systems for high-quality clinical CAR T-cell products. This review discusses current and novel CAR T-cell processing methodologies and the quality control systems needed to meet the increasing clinical demand for these exciting new therapies.
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