Established bioprocesses for producing antibodies as a basis for future planning

被引:34
作者
Farid, Suzanne S. [1 ]
机构
[1] UCL, Dept Biochem Engn, Adv Ctr Biochem Engn, London WC1E 7JE, England
来源
CELL CULTURE ENGINEERING | 2006年 / 101卷
关键词
antibody production/manufacture; antibody fragments; mammalian cell culture; therapeutic and diagnostic antibodies; transgenic;
D O I
10.1007/10_014
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
In the early years of monoclonal antibody production for human therapy and diagnosis the methods used were arrived at by individual organisations. However, there is now an accumulating body of information on antibodies and fragments that have been produced by processes approved for human use. This information is becoming available at a time when the number of potential antibody-based medicines is growing sharply. The review addresses the reported production routes, their scale and the titres achieved. It identifies the performances of fed-batch and perfusion culture versus batch culture, and compares processes for the production of antibodies for diagnosis and for antibody fragments. The analysis defines the likely routes of future production in a sector where demanding regulations constrain new technology. It also indicates what levels of performance new approaches will need to meet to be competitive.
引用
收藏
页码:1 / 42
页数:42
相关论文
共 82 条
[1]  
*AM PHARM BIOT, 1999, DOWNSTREAM, V30, P22
[2]  
Behizad M, 2000, BIOPHARM-APPL T BIO, V13, P42
[3]   IN PURSUIT OF THE OPTIMAL FED-BATCH PROCESS FOR MONOCLONAL-ANTIBODY PRODUCTION [J].
BIBILA, TA ;
ROBINSON, DK .
BIOTECHNOLOGY PROGRESS, 1995, 11 (01) :1-13
[4]  
Birch J. R., 1995, P231
[5]  
BIRCH JR, 1987, MONOCLONAL ANTIBODIE, P55
[6]  
BIRCH JR, 1999, ENCY BIOPROCESS TECH, V1
[7]  
BIRCH JR, 1999, ENCY BIOPROCESS TECH, V5
[8]  
Boothe JG, 1997, DRUG DEVELOP RES, V42, P172, DOI 10.1002/(SICI)1098-2299(199711/12)42:3/4<172::AID-DDR9>3.0.CO
[9]  
2-N
[10]   Therapeutic antibodies for human diseases at the dawn of the twenty-first century [J].
Brekke, OH ;
Sandlie, I .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (01) :52-62