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首页> 外文期刊>Human gene therapy >Large-Scale Adeno-Associated Viral Vector Production Using a Herpesvirus-Based System Enables Manufacturing for Clinical Studies
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Large-Scale Adeno-Associated Viral Vector Production Using a Herpesvirus-Based System Enables Manufacturing for Clinical Studies

机译:使用基于疱疹病毒的系统进行大规模腺相关病毒载体生产可用于临床研究

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摘要

The ability of recombinant adeno-associated viral (rAAV) vectors to exhibit minimal immunogenicity and little to no toxicity or inflammation while eliciting robust, multiyear gene expression in vivo are only a few of the salient features that make them ideally suited for many gene therapy applications. A major hurdle for the use of rAAV in sizeable research and clinical applications is the lack of efficient and versatile large-scale production systems. Continued progression toward flexible, scalable production techniques is a prerequisite to support human clinical evaluation of these novel biotherapeutics. This review examines the current state of large-scale production methods that employ the herpes simplex virus type 1 (HSV) platform to produce rAAV vectors for gene delivery. Improvements have substantially advanced the HSV/AAV hybrid method for large-scale rAAV manufacture, facilitating the generation of highly potent, clinical-grade purity rAAV vector stocks. At least one human clinical trial employing rAAV generated via rHSV helper-assisted replication is poised to commence, highlighting the advances and relevance of this production method.
机译:重组腺相关病毒(rAAV)载体表现出最小的免疫原性,几乎没有毒性或无炎症,同时在体内引起稳定,​​多年的基因表达的能力只是其中几个突出特征,使其非常适合于许多基因治疗应用。在大规模研究和临床应用中使用rAAV的主要障碍是缺乏有效和通用的大规模生产系统。不断朝着灵活,可扩展的生产技术发展是支持人类对这些新型生物疗法进行临床评估的先决条件。这项审查审查了大规模生产方法的现状,这些方法采用1型单纯疱疹病毒(HSV)平台生产用于基因传递的rAAV载体。改进已大大推进了用于大规模rAAV制造的HSV / AAV混合方法,从而促进了高效,临床级纯度的rAAV载体库的产生。至少一项采用通过rHSV辅助复制产生的rAAV的人类临床试验即将开始,这突显了这种生产方法的进步和相关性。

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