Oxford BioMedica, Oxford OX4 4GA, United Kingdom.
Hum Gene Ther. 2011 Mar;22(3):357-69. doi: 10.1089/hum.2010.142. Epub 2011 Feb 10.
ProSavin is an equine infectious anemia virus vector-based gene therapy for Parkinson's disease for which inducible HEK293T-based producer cell lines (PCLs) have been developed. These cell lines demonstrate stringent tetracycline-regulated expression of the packaging components and yield titers comparable to the established transient production system. A prerequisite for the use of PCL-derived lentiviral vectors (LVs) in clinical applications is the thorough characterization of both the LV and respective PCL with regard to identity and genetic stability. We describe the detailed characterization of two ProSavin PCLs (PS5.8 and PS46.2) and resultant ProSavin vector. The two cell lines demonstrate stable production of vector over a time period sufficient to allow generation of master and working cell banks, and subsequent large-scale vector production. ProSavin generated from the PCLs performs comparably in vivo to that produced by the standard transient transfection process with respect to transduction efficiency and immunogenicity. The development of ProSavin PCLs, and the detailed characterization described here, will aid the advancement of ProSavin for clinical application.
ProSavin 是一种马传染性贫血病毒载体基因治疗帕金森病的药物,已开发出可诱导的 HEK293T 生产细胞系 (PCL)。这些细胞系表现出严格的四环素调控的包装组件表达,并产生与已建立的瞬时生产系统相当的滴度。PCL 衍生的慢病毒载体 (LV) 在临床应用中的一个前提条件是对 LV 和相应的 PCL 进行彻底的鉴定和遗传稳定性特征分析。我们描述了两个 ProSavin PCL(PS5.8 和 PS46.2)和相应的 ProSavin 载体的详细特征。这两个细胞系在足够长的时间内稳定地生产载体,足以允许生成主细胞库和工作细胞库,以及随后的大规模载体生产。从 PCL 产生的 ProSavin 在体内与通过标准瞬时转染过程产生的 ProSavin 在转导效率和免疫原性方面相当。ProSavin PCL 的开发以及这里描述的详细特征分析将有助于推进 ProSavin 用于临床应用。