遗传增强
病毒载体
转导(生物物理学)
HEK 293细胞
细胞培养
转染
载体(分子生物学)
生物
细胞
计算生物学
病毒学
基因
遗传学
重组DNA
生物化学
作者
Hannah J. Stewart,Liang Fong-Wong,Iain Strickland,Daniel Chipchase,Michelle Kelleher,Laura Stevenson,Vinay Thoree,Janine McCarthy,G. Ralph,Kyriacos Mitrophanous,Pippa A. Radcliffe
出处
期刊:Human Gene Therapy
[Mary Ann Liebert, Inc.]
日期:2010-11-11
卷期号:22 (3): 357-369
被引量:38
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI