A Stable Producer Cell Line for the Manufacture of a Lentiviral Vector for Gene Therapy of Parkinson's Disease

被引:23
|
作者
Stewart, Hannah J. [1 ]
Fong-Wong, Liang [2 ]
Strickland, Iain [2 ]
Chipchase, Daniel [1 ]
Kelleher, Michelle [1 ]
Stevenson, Laura [1 ]
Thoree, Vinay [1 ]
McCarthy, Janine [1 ]
Ralph, G. Scott [1 ]
Mitrophanous, Kyriacos A. [1 ]
Radcliffe, Pippa A. [1 ]
机构
[1] Oxford BioMed UK Ltd, Medawar Ctr, Oxford OX4 4GA, England
[2] Univ Bristol, Henry Wellcome Labs Integrat Neurosci & Endocrino, Bristol BS1 3NY, Avon, England
关键词
REPLICATION-COMPETENT LENTIVIRUS; LARGE-SCALE PRODUCTION; HIGH-TITER; NERVOUS-SYSTEM; RETROVIRAL VECTORS; GENERATION; DELIVERY; EXPRESSION;
D O I
10.1089/hum.2010.142
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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.
引用
收藏
页码:357 / 369
页数:13
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