Generation of monoclonal antibody-producing mammalian cell lines

被引:33
作者
Ho, Steven C. L. [1 ,2 ]
Tong, Yen Wah [2 ]
Yang, Yuansheng [1 ,3 ]
机构
[1] Agcy Sci Technol & Res, Bioproc Technol Inst, 20 Biopolis Way,06-01 Centros, Singapore 138668, Singapore
[2] Natl Univ Singapore, Dept Bioengn, Dept Chem & Biomol Engn, Singapore 119620, Singapore
[3] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
关键词
D O I
10.4155/PBP.13.8
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
Clinical effectiveness has driven the commercial success of monoclonal antibody (mAb) products. Mammalian cells are currently the preferred system for large-scale production as the mAbs produced are biochemically similar to human forms. The cell line generation process is tedious and time-consuming as clones with high productivity, stable long-term expression and good product quality are rare occurrences. Cell line generation efficiency and mAb quality can be improved through host cell engineering, vector optimization and high-throughput clone selection. Targeted integration into predetermined sites on the chromosome is a promising new area being explored. This review covers existing technology and recent progress made in improving various aspects of the stable cell line generation process for mAb production.
引用
收藏
页码:71 / 87
页数:17
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