## Abstract In this study we compare the cellular control of recombinant human IgG~4~ monoclonal antibody (Mab) synthesis in different CHO cell lines. Based on comprehensive empirical analyses of mRNA and polypeptide synthetic intermediates we constructed cell line‐specific mathematical models of r
Production of target-specific recombinant human polyclonal antibodies in mammalian cells
✍ Scribed by Finn C. Wiberg; Søren K. Rasmussen; Torben P. Frandsen; Lone K. Rasmussen; Kaja Tengbjerg; Vincent W. Coljee; Jacqueline Sharon; Chiou-Ying Yang; Søren Bregenholt; Lars S. Nielsen; John S. Haurum; Anne B. Tolstrup
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 494 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0006-3592
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We describe the expression and consistent production of a first target‐specific recombinant human polyclonal antibody. An anti‐Rhesus D recombinant polyclonal antibody, Sym001, comprised of 25 unique human IgG1 antibodies, was produced by the novel Sympress expression technology. This strategy is based on site‐specific integration of antibody genes in CHO cells, using the FRT/Flp‐In recombinase system. This allows integration of the expression construct at the same genomic site in the host cells, thereby reducing genomic position effects. Different bioreactor batches of Sym001 displayed highly consistent manufacturing yield, antibody composition, binding potency, and functional activity. The results demonstrate that diverse recombinant human polyclonal antibody compositions can be reproducibly generated under conditions directly applicable to industrial manufacturing settings and present a first recombinant polyclonal antibody which could be used for treatment of hemolytic disease of the newborn and/or idiopathic thrombocytopenic purpura. © 2006 Wiley Periodicals, Inc.
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