Recent advances in upstream process development for production of recombinant adeno-associated virus

被引:12
作者
Ou, Jianfa [1 ]
Tang, Yawen [1 ]
Xu, Jianlin [1 ]
Tucci, Julian [1 ]
Borys, Michael C. [1 ]
Khetan, Anurag [1 ]
机构
[1] Bristol Myers Squibb, Biol Dev Global Prod Dev & Supply, Devens, MA 01434 USA
关键词
bioreactor; medium optimization; rAAV manufacturing; upstream process control; SERUM-FREE PRODUCTION; LENTIVIRAL VECTOR PRODUCTION; HIGHLY EFFICIENT PRODUCTION; LARGE-SCALE PRODUCTION; HIGH-YIELD PRODUCTION; TRANSIENT TRANSFECTION; GENE-THERAPY; VIRAL VECTOR; SCALABLE PRODUCTION; INSECT CELLS;
D O I
10.1002/bit.28545
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
Recombinant adeno-associated virus (rAAV) is rapidly emerging as the preferred delivery vehicle for gene therapies, with promising advantages in safety and efficacy. Key challenges in systemic in-vivo rAAV gene therapy applications are the gap in production capabilities versus potential market demand and complex production process. This review summarizes current available information on rAAV upstream manufacturing processes and proposed optimizations for production. The advancements in rAAV production media were reviewed with proposals to speed up the cell culture process development. Furthermore, major methods for genetic element delivery to host cells were summarized with their advantages, limitations, and future directions for optimization. In addition, culture vessel selection criteria were listed based on production cell system, scale, and development stage. Process control at the production step was also outlined with an in-depth understanding of production kinetics and quality control. Advancement of upstream process development is described to overcome the challenges for complex recombinant adeno-associated virus production. Public information and trends in four major areas, that is, cell culture media, genetic element delivery to host cell, culture vessel (a.k.a bioreactor) selection, and process control at the production step were summarized targeting a high yield and high-quality process. The advantages and limitations of each technology were evaluated as part of process robustness assessment.image
引用
收藏
页码:53 / 70
页数:18
相关论文
共 128 条
[41]   Optimization of recombinant adeno-associated virus production using an herpes simplex virus amplicon system [J].
Feudner, E ;
de Alwis, M ;
Thrasher, AJ ;
Ali, RR ;
Fauser, S .
JOURNAL OF VIROLOGICAL METHODS, 2001, 96 (02) :97-105
[42]   Accurate Titration of Infectious AAV Particles Requires Measurement of Biologically Active Vector Genomes and Suitable Controls [J].
Francois, Achille ;
Bouzelha, Mohammed ;
Lecomte, Emilie ;
Broucque, Frederic ;
Penaud-Budloo, Magalie ;
Adjali, Oumeya ;
Moullier, Philippe ;
Blouin, Veronique ;
Ayuso, Eduard .
MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT, 2018, 10 :223-236
[43]   A BRIEF-HISTORY OF GENE-THERAPY [J].
FRIEDMANN, T .
NATURE GENETICS, 1992, 2 (02) :93-98
[44]   Rep/cap gene amplification and high-yield production of AAV in an A549 cell line expressing rep/cap [J].
Gao, GP ;
Lu, FM ;
Sanmiguel, JC ;
Tran, PT ;
Abbas, Z ;
Lynd, KS ;
Marsh, J ;
Spinner, NB ;
Wilson, JM .
MOLECULAR THERAPY, 2002, 5 (05) :644-649
[45]   Reflections on more than 10 years of TGE approaches [J].
Geisse, Sabine .
PROTEIN EXPRESSION AND PURIFICATION, 2009, 64 (02) :99-107
[46]   Impact of physicochemical properties of DNA/PEI complexes on transient transfection of mammalian cells [J].
Gonzalez-Dominguez, I. ;
Grimaldi, N. ;
Cervera, L. ;
Ventosa, N. ;
Godia, F. .
NEW BIOTECHNOLOGY, 2019, 49 :88-97
[47]   Production of Recombinant Adeno-associated Virus Vectors Using Suspension HEK293 Cells and Continuous Harvest of Vector From the Culture Media for GMP FIX and FLT1 Clinical Vector [J].
Grieger, Joshua C. ;
Soltys, Stephen M. ;
Samulski, Richard Jude .
MOLECULAR THERAPY, 2016, 24 (02) :287-297
[48]   Preclinical in vivo evaluation of pseudotyped adeno-associated virus vectors for liver gene therapy [J].
Grimm, D ;
Zhou, SZ ;
Nakai, H ;
Thomas, CE ;
Storm, TA ;
Fuess, S ;
Matsushita, T ;
Allen, J ;
Surosky, R ;
Lochrie, M ;
Meuse, L ;
McClelland, A ;
Colosi, P ;
Kay, MA .
BLOOD, 2003, 102 (07) :2412-2419
[49]  
Guillemin Z., 2020, GROWTH, V2
[50]   Efficient production of recombinant adeno-associated viral vector, serotype DJ/8, carrying the GFP gene [J].
Hashimoto, Haruo ;
Mizushima, Tomoko ;
Chijiwa, Tsuyoshi ;
Nakamura, Masato ;
Suemizu, Hiroshi .
VIRUS RESEARCH, 2017, 238 :63-68