摘要
嵌合抗原受体T细胞治疗产品的上市,标志着个体化治疗进入了一个新阶段。但因该类产品生产工艺复杂,相关产业链尚未真正成熟,而此产业现又处在快速发展的上升阶段,整个业界存在一定的人才缺口,对产品上市后的质量管理和监管提出了挑战。本文从嵌合抗原受体T细胞治疗产品的特点出发,分析该类产品在防混淆、防污染方面面临的问题,以期业界加强质量管理,确保产品质量和安全。
The marketing authorization of chimeric antigen receptor T cell(CAR-T)therapy products marks that the individualized therapy has entered a new stage.However,the relevant industrial chain has not really matured due to the complex production process of such products.Although this industry is now in the rising stage of rapid development,the whole industry poses a challenge to the quality management and supervision of products after marketing because there exists a certain talent gap.This paper analyzes the problems faced by these products to be prevented from mix-up and contamination so as to strengthen the quality management and ensure the product quality and safety based on the characteristics of CAR-T therapy products.
作者
丁力承
金德庄
李香玉
DING Licheng;JIN Dezhuang;LI Xiangyu(Shanghai Center for Drug Evaluation and Inspection,Shanghai 201203,China)
出处
《上海医药》
CAS
2022年第11期11-13,共3页
Shanghai Medical & Pharmaceutical Journal
关键词
嵌合抗原受体T
细胞
质量管理
药品监管
chimeric antigen receptor T cell
quality management
drug regulation