Translational Glycomics Research Group, Research Institute of Biomolecular and Chemical Engineering, University of Pannonia, Veszprem, Egyetem u. 10, Hungary.
Curr Mol Med. 2020;20(10):806-813. doi: 10.2174/1566524020999200730181042.
Adeno-associated virus (AAV) is one of the most promising viral gene delivery vectors with long-term gene expression and disease correction, featuring high efficiency and excellent safety in human clinical trials. During the production of AAV vectors, there are several quality control (QC) parameters that should be rigorously monitored to comply with clinical safety and efficacy. This review gives a short summary of the most frequently used AVV production and purification methods, focusing on the analytical techniques applied to determine the full/empty capsid ratio and the integrity of the encapsidated therapeutic DNA of the products.
腺相关病毒(AAV)是最有前途的病毒基因传递载体之一,具有长期的基因表达和疾病纠正作用,在人体临床试验中具有高效和极好的安全性。在 AAV 载体的生产过程中,有几个质量控制(QC)参数需要严格监测,以符合临床安全性和疗效的要求。本文简要总结了最常使用的 AAV 生产和纯化方法,重点介绍了用于确定产品的完整/空衣壳比和包裹的治疗性 DNA 完整性的分析技术。