中国仓鼠卵巢细胞
重组DNA
因子IX
化学
生物化学
分子生物学
生物
基因
受体
作者
Scott H. Harrison,S. Robert Adamson,D Bonam,Scott R. Brodeur,Timothy S. Charlebois,Brian M. Clancy,Ruth Costigan,Denis Drapeau,Matthew J. Hamilton,Kathryn A. Hanley,Brian D. Kelley,A. Knight,Martin O. Leonard,Micheline McCarthy,Patrick W. Oakes,K Sterl,Mary E. Switzer,Richard M. Walsh,William R. Foster
出处
期刊:PubMed
日期:1998-04-01
卷期号:35 (2 Suppl 2): 4-10
被引量:66
摘要
Advances in recombinant DNA manufacturing technology have now made possible the production of a highly purified and active recombinant factor IX (rFIX) product. Recombinant factor IX was developed by (1) stable insertion of the genes for both factor IX and PACE-SOL (a truncated, soluble serine protease needed to enhance the capacity of cells to remove the amino-terminal propeptide from rFIX) into Chinese hamster ovary cells; (2) selection of a cell line that was capable of expressing high amounts of active rFIX while growing in bioreactors containing a completely defined culture medium that does not contain blood or plasma products; and (3) inclusion of four independent chromatography steps, none of which require monoclonal antibodies. Furthermore, rFIX has been extensively tested to demonstrate similarity to plasma-derived factor IX and has been shown to be a consistent, high-purity product. For example, a high-specific-activity product (276+/-23 IU/mg) has been consistently produced throughout 65 consecutive batches from five consecutive manufacturing campaigns. Thus, rFIX offers a consistent and high-purity source of factor IX treatment for patients with hemophilia B.
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