Cell culture processes for monoclonal antibody production

被引:492
作者
Li, Feng [1 ]
Vijayasankaran, Natarajan [2 ]
Shen, Amy [3 ]
Kiss, Robert [2 ]
Amanullah, Ashraf [1 ]
机构
[1] Genentech Inc, Pharma Tech Dev US Biol, Oceanside Pharma Tech Dev, Oceanside, CA USA
[2] Genentech Inc, Pharma Tech Dev US Biol, Late Stage Cell Culture, San Francisco, CA 94080 USA
[3] Genentech Inc, Pharma Tech Dev US Biol, Early Stage Cell Culture, San Francisco, CA 94080 USA
关键词
monoclonal antibody; expression systems; cell line engineering; cell culture process development; optimization scale-up and technology transfer; process advances; RECOMBINANT PROTEIN THERAPEUTICS; DISSOLVED-OXYGEN CONCENTRATION; HIGH-LEVEL EXPRESSION; HAMSTER OVARY CELLS; SCALE-DOWN MODEL; HYBRIDOMA GROWTH; INTERFERON-GAMMA; DEFINED PROTEIN; NS0; CELLS; DENSITY;
D O I
10.4161/mabs.2.5.12720
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Animal cell culture technology has advanced significantly over the last few decades and is now generally considered a reliable, robust and relatively mature technology. A range of biotherapeutics are currently synthesized using cell culture methods in large scale manufacturing facilities that produce products for both commercial use and clinical studies. The robust implementation of this technology requires optimization of a number of variables, including (1) cell lines capable of synthesizing the required molecules at high productivities that ensure low operating cost; (2) culture media and bioreactor culture conditions that achieve both the requisite productivity and meet product quality specifications; (3) appropriate online and off-line sensors capable of providing information that enhances process control; and (4) good understanding of culture performance at different scales to ensure smooth scale-up. Successful implementation also requires appropriate strategies for process development, scale-up and process characterization and validation that enable robust operation and ensure compliance with current regulations. This review provides an overview of the state-of-the art technology in key aspects of cell culture, e.g., generation of highly productive cell lines and optimization of cell culture process conditions. We also summarize the current thinking on appropriate process development strategies and process advances that might affect process development.
引用
收藏
页码:466 / 479
页数:14
相关论文
共 105 条
[81]  
2-6
[82]   The production of monoclonal antibody in growth-arrested hybridomas cultivated in suspension and immobilized modes [J].
Seifert, DB ;
Phillips, JA .
BIOTECHNOLOGY PROGRESS, 1999, 15 (04) :655-666
[83]   Reverting cholesterol auxotrophy of NS0 cells by altering epigenetic gene silencing [J].
Seth, G ;
Ozturk, M ;
Hu, WS .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 93 (04) :820-827
[84]   Molecular portrait of high productivity in recombinant NS0 cells [J].
Seth, Gargi ;
Philp, Robin J. ;
Lau, Ally ;
Jiun, Kok Yee ;
Yap, Miranda ;
Hu, Wei-Shou .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 97 (04) :933-951
[85]  
Shen AY, 2006, BIOTECHNOL & BIOPROC, V30, P15
[86]   Expression of full-length immunoglobulins in Escherichia coli:: rapid and efficient production of aglycosylated antibodies [J].
Simmons, LC ;
Reilly, D ;
Klimowski, L ;
Raju, TS ;
Meng, G ;
Sims, P ;
Hong, K ;
Shields, RL ;
Damico, LA ;
Rancatore, P ;
Yansura, DG .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 263 (1-2) :133-147
[87]   Defined protein and animal component-free NSO fed-batch culture [J].
Spens, Erika ;
Haeggstroem, Lena .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 98 (06) :1183-1194
[88]   Human uptake and incorporation of an immunogenic nonhuman dietary sialic acid [J].
Tangvoranuntakul, P ;
Gagneux, P ;
Diaz, S ;
Bardor, M ;
Varki, N ;
Varki, A ;
Muchmore, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) :12045-12050
[89]  
Vijayasankaran N., 2010, ENCY IND BIOTECHNOLO
[90]   Post-translational modifications in the context of therapeutic proteins [J].
Walsh, Gary ;
Jefferis, Roy .
NATURE BIOTECHNOLOGY, 2006, 24 (10) :1241-1252