生物过程
中国仓鼠卵巢细胞
重组DNA
因子IX
生物技术
生物
细胞培养
生物化学
遗传学
基因
古生物学
作者
Aiden C. Beauglehole,Dinora Roche Recinos,Cassandra L. Pegg,Yih Yean Lee,Victor Turnbull,Susann Herrmann,Esteban Marcellin,Christopher B. Howard,Benjamin L. Schulz
标识
DOI:10.1080/07388551.2022.2036691
摘要
Appropriate treatment of Hemophilia B is vital for patients' quality of life. Historically, the treatment used was the administration of coagulation Factor IX derived from human plasma. Advancements in recombinant technologies allowed Factor IX to be produced recombinantly. Successful recombinant production has triggered a gradual shift from the plasma derived origins of Factor IX, as it provides extended half-life and expanded production capacity. However, the complex post-translational modifications of Factor IX have made recombinant production at scale difficult. Considerable research has therefore been invested into understanding and optimizing the recombinant production of Factor IX. Here, we review the evolution of recombinant Factor IX production, focusing on recent developments in bioprocessing and cell engineering to control its post-translational modifications in its expression from Chinese Hamster Ovary (CHO) cells.
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