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
[1]   Affecting HEK293 Cell Growth and Production Performance by Modifying the Expression of Specific Genes [J].
Abaandou, Laura ;
Quan, David ;
Shiloach, Joseph .
CELLS, 2021, 10 (07)
[2]   Sodium Chloride Enhances Recombinant Adeno-Associated Virus Production in a Serum-Free Suspension Manufacturing Platform Using the Herpes Simplex Virus System [J].
Adamson-Small, Laura ;
Potter, Mark ;
Byrne, Barry J. ;
Clement, Nathalie .
HUMAN GENE THERAPY METHODS, 2017, 28 (01) :1-14
[3]   A scalable method for the production of high-titer and high-quality adeno-associated type 9 vectors using the HSV platform [J].
Adamson-Small, Laura ;
Potter, Mark ;
Falk, Darin J. ;
Cleaver, Brian ;
Byrne, Barry J. ;
Clement, Nathalie .
MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT, 2016, 3 :16031
[4]   Process intensification for the production of yellow fever virus-like particles as potential recombinant vaccine antigen [J].
Alvim, Renata G. F. ;
Lima, Tulio M. ;
Silva, Jerson L. ;
de Oliveira, Guilherme A. P. ;
Castilho, Leda R. .
BIOTECHNOLOGY AND BIOENGINEERING, 2021, 118 (09) :3581-3592
[5]   Development of a scalable process for high-yield lentiviral vector production by transient transfection of HEK293 suspension cultures [J].
Ansorge, Sven ;
Lanthier, Stephane ;
Transfiguracion, Julia ;
Durocher, Yves ;
Henry, Olivier ;
Kamen, Amine .
JOURNAL OF GENE MEDICINE, 2009, 11 (10) :868-876
[6]   An inducible system for highly efficient production of recombinant adeno-associated virus (rAAV) vectors in insect Sf9 cells [J].
Aslanidi, George ;
Lamb, Kenneth ;
Zolotukhin, Sergei .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (13) :5059-5064
[7]   Critical assessment of current adeno-associated viral vector production and quantification methods [J].
Aucoin, Marc G. ;
Perrier, Michel ;
Kamen, Amine A. .
BIOTECHNOLOGY ADVANCES, 2008, 26 (01) :73-88
[8]   Improving AAV vector yield in insect cells by modulating the temperature after infection [J].
Aucoin, Marc G. ;
Perrier, Michel ;
Kamen, Amine A. .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 97 (06) :1501-1509
[9]   Production of adeno-associated viral vectors in insect cells using triple infection: Optimization of baculovirus concentration ratios [J].
Aucoin, Marc G. ;
Perrier, Michel ;
Kamen, Amine A. .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 95 (06) :1081-1092
[10]   Production, Purification and Characterization of Adeno-Associated Vectors [J].
Ayuso, Eduard ;
Mingozzi, Federico ;
Bosch, Fatima .
CURRENT GENE THERAPY, 2010, 10 (06) :423-436