嵌合抗原受体
食品药品监督管理局
临床试验
医学
过继性细胞移植
淋巴瘤
细胞疗法
CD19
免疫学
癌症研究
T细胞
抗原
药理学
生物
细胞
内科学
免疫系统
遗传学
作者
Ulrike Köhl,Stanislava Arsenieva,Astrid Holzinger,Hinrich Abken
出处
期刊:Human Gene Therapy
[Mary Ann Liebert]
日期:2018-05-01
卷期号:29 (5): 559-568
被引量:85
摘要
The adoptive transfer of chimeric antigen receptor (CAR)-modified T cells is attracting growing interest for the treatment of malignant diseases. Early trials with anti-CD19 CAR T cells have achieved spectacular remissions in B-cell leukemia and lymphoma, so far refractory, very recently resulting in the Food and Drug Administration approval of CD19 CAR T cells for therapy. With further applications and increasing numbers of patients, the reproducible manufacture of high-quality clinical-grade CAR T cells is becoming an ever greater challenge. New processing techniques, quality-control mechanisms, and logistic developments are required to meet both medical needs and regulatory restrictions. This paper summarizes the state-of-the-art in manufacturing CAR T cells and the current challenges that need to be overcome to implement this type of cell therapy in the treatment of a variety of malignant diseases and in a greater number of patients.
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