Insect Cell-Based Recombinant Adeno-Associated Virus Production: Molecular Process Optimization

J. Lubelski, W. Hermens, H. Petry
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引用次数: 0

Abstract

A n increasing number of clinical trials, and the recent approval of the first gene therapy in Europe, alipogene tiparvovec (Glybera®, uniQure), holds promise for recombinant adeno-associated virus (rAAV) to become a mainstay in clinical practice. Since the molecular cloning of AAV in the 1980s, a plethora of production protocols/manufacturing systems for generating rAAV vectors have been developed. uniQure’s manufacturing platform, which has received validation through regulatory approval, is also capable of supporting industrial-scale production based on the baculovirus expression vector system (BEVS) and insect cells. In this paper, we review the molecular process optimization of the various components of uniQure’s rAAV production platform.
基于昆虫细胞的重组腺相关病毒生产:分子过程优化
越来越多的临床试验,以及最近在欧洲批准的首个基因疗法,alipogene tiparvovec (Glybera®,独特),有望使重组腺相关病毒(rAAV)成为临床实践的支柱。自20世纪80年代AAV分子克隆以来,已经开发了大量用于生成rAAV载体的生产协议/制造系统。unique的生产平台已经通过监管部门的批准,也能够支持基于杆状病毒表达载体系统(BEVS)和昆虫细胞的工业规模生产。本文综述了unique rAAV生产平台各部件的分子工艺优化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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