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重组凝血因子IX的制造工艺。

The manufacturing process for recombinant factor IX.

作者信息

Harrison S, Adamson S, Bonam D, Brodeur S, Charlebois T, Clancy B, Costigan R, Drapeau D, Hamilton M, Hanley K, Kelley B, Knight A, Leonard M, McCarthy M, Oakes P, Sterl K, Switzer M, Walsh R, Foster W

机构信息

Genetics Institute, Inc, Andover, MA 01810, USA.

出版信息

Semin Hematol. 1998 Apr;35(2 Suppl 2):4-10.

PMID:9565160
Abstract

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.

摘要

重组DNA制造技术的进步现已使生产高度纯化且具有活性的重组凝血因子IX(rFIX)产品成为可能。重组凝血因子IX是通过以下方式开发的:(1)将凝血因子IX和PACE-SOL(一种截短的可溶性丝氨酸蛋白酶,用于增强细胞从rFIX中去除氨基末端前肽的能力)的基因稳定插入中国仓鼠卵巢细胞;(2)选择一种细胞系,该细胞系能够在含有完全确定的培养基(不含血液或血浆制品)的生物反应器中生长时表达大量活性rFIX;(3)采用四个独立的色谱步骤,其中任何一个步骤都不需要单克隆抗体。此外,rFIX已进行了广泛测试,以证明其与血浆来源的凝血因子IX相似,并且已被证明是一种稳定的高纯度产品。例如,在连续五个生产批次的65个连续批次中,始终生产出高比活性产品(276±23 IU/mg)。因此,rFIX为B型血友病患者提供了一种稳定且高纯度的凝血因子IX治疗来源。

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