Manufacturing Recombinant Adeno-Associated Viral Vectors from Producer Cell Clones

被引:58
作者
Thorne, Barbara A. [1 ]
Takeya, Ryan K. [1 ]
Peluso, Richard W. [1 ]
机构
[1] Targeted Genetics Corp, Seattle, WA 98101 USA
关键词
VIRUS REP PROTEINS; HIGH-TITER; GENE AMPLIFICATION; HELPER FUNCTIONS; HELA-CELLS; AAV; LINES; ADENOVIRUS; EXPRESSION; SEQUENCES;
D O I
10.1089/hum.2009.070
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
A commercial rAAV manufacturing process needs to provide a safe product at high yield, be easily scalable, regulatory-compliant, and have reasonable cost of goods. Considerations for process development include not only product quantity and quality, but also ease of obtaining equipment, performing validation, and demonstrating control. In these regards, it is usually efficient to make use of proven technologies for more established areas of manufacturing, such as cell culture and purification methods used by the recombinant protein/monoclonal antibody industry. We have focused on stable mammalian producer cell lines with adenovirus type 5 helper virus as a means of achieving these goals. This review describes our current approach for generating producer cell clones and designing a scalable, regulatory-compliant vector production and purification process that addresses any product safety concerns relating to helper virus. To date, a producer cell line-based manufacturing process has been implemented at the 250-liter production scale, with no foreseeable impediments to scaling up to commercial vector manufacturing in 2000-liter bioreactors or larger.
引用
收藏
页码:707 / 714
页数:8
相关论文
共 35 条
[1]   Definition of Herpes Simplex Virus Type 1 Helper Activities for Adeno-Associated Virus Early Replication Events [J].
Alazard-Dany, Nathalie ;
Nicolas, Armel ;
Ploquin, Aurelie ;
Strasser, Regina ;
Greco, Anna ;
Epstein, Alberto L. ;
Fraefel, Cornel ;
Salvetti, Anna .
PLOS PATHOGENS, 2009, 5 (03)
[2]   Identification and elimination of replication-competent adeno-associated virus (AAV) that can arise by nonhomologous recombination during AAV vector production [J].
Allen, JM ;
Debelak, DJ ;
Reynolds, TC ;
Miller, AD .
JOURNAL OF VIROLOGY, 1997, 71 (09) :6816-6822
[3]   Replication competent helper functions for recombinant AAV vector generation [J].
Cao, L ;
During, M ;
Xiao, W .
GENE THERAPY, 2002, 9 (18) :1199-1206
[4]   High-titer, wild-type free recombinant adeno-associated virus vector production using intron-containing helper plasmids [J].
Cao, L ;
Liu, YH ;
During, MJ ;
Xiao, WD .
JOURNAL OF VIROLOGY, 2000, 74 (24) :11456-11463
[5]   Evidence for encapsidation of prokaryotic sequences during recombinant adeno-associated virus production and their in vivo persistence after vector delivery [J].
Chadeuf, G ;
Ciron, C ;
Moullier, P ;
Salvetti, A .
MOLECULAR THERAPY, 2005, 12 (04) :744-753
[6]  
Chadeuf G, 2000, J GENE MED, V2, P260
[7]   CELL-LINES FOR THE PRODUCTION OF RECOMBINANT ADENOASSOCIATED VIRUS [J].
CLARK, KR ;
VOULGAROPOULOU, F ;
FRALEY, DM ;
JOHNSON, PR .
HUMAN GENE THERAPY, 1995, 6 (10) :1329-1341
[8]   Development and characterization of a cell line for large-scale, serum-free production of recombinant adeno-associated viral vectors [J].
Farson, D ;
Harding, TC ;
Tao, L ;
Liu, J ;
Powell, S ;
Vimal, V ;
Yendluri, S ;
Koprivnikar, K ;
Ho, K ;
Twitty, C ;
Husak, P ;
Lin, A ;
Snyder, RO ;
Donahue, BA .
JOURNAL OF GENE MEDICINE, 2004, 6 (12) :1369-1381
[9]  
FDA (Food and Drug Administration) . US Department of Health and Human Services Center for Biologics Evaluation and Research (CBER) Pharmacology and Toxicology, 2008, GUID FDA REV SPONS C
[10]   High-titer adeno-associated viral vectors from a Rep/Cap cell line and hybrid shuttle virus [J].
Gao, GP ;
Qu, G ;
Faust, LZ ;
Engdahl, RK ;
Xiao, WD ;
Hughes, JV ;
Zoltick, PW ;
Wilson, JM .
HUMAN GENE THERAPY, 1998, 9 (16) :2353-2362