Manufacturing of viral vectors: part II. Downstream processing and safety aspects

O. Merten, M. Schweizer, P. Chahal, A. Kamen
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引用次数: 28

Abstract

Manufacturing of viral vectors comprises the generation of these vectors, which then have to be purified in order to meet the quality attributes required for further use as gene delivery systems. The first part of this article deals with the production of the most important viral vectors used in gene therapy protocols. In the second part, we briefly review the most current methods used for the purification of viral gene therapy products focusing on four viral vectors that have been the most extensively used in clinical trials: adenoviral, adeno-associated viral and lentiviral vectors. Traditionally, γ-retroviral vectors were not purified and clarified vectors containing culture supernatant was directly used for ex vivo gene therapy. The final section of this article reviews some of the basic biosafety considerations specific to the respective viral vectors.
病毒载体的制造:第二部分。下游加工和安全方面
病毒载体的制造包括这些载体的产生,然后必须对其进行纯化,以满足进一步用作基因传递系统所需的质量属性。本文的第一部分涉及基因治疗方案中使用的最重要的病毒载体的生产。在第二部分中,我们简要回顾了目前用于病毒基因治疗产品纯化的最新方法,重点介绍了在临床试验中应用最广泛的四种病毒载体:腺病毒、腺相关病毒和慢病毒载体。传统上,γ-逆转录病毒载体未经纯化,含有培养上清的澄清载体直接用于离体基因治疗。本文的最后一节回顾了一些基本的生物安全考虑具体到各自的病毒载体。
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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