[通过基因技术生产因子VIII]。

O Neutzling
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引用次数: 0

摘要

分离出人VIII因子基因和人血管性血血病因子基因,并转染到哺乳动物卵巢细胞系(中国仓鼠卵巢细胞= CHO细胞)中。所得到的因子VIII产生细胞系进行了彻底的表征。重组因子VIII与血浆源性因子VIII没有差异。为了生产因子VIII,细胞在无血清培养基中生长,重组因子VIII通过免疫亲和层析和随后的两个离子交换步骤纯化。由于不需要人类生产原料,且纯化过程中已证实滴度降低了> 10(7),因此重组因子VIII产品传播病毒的风险显著降低。对既往治疗和未治疗患者的临床研究均证明重组因子VIII具有良好的止血疗效和病毒安全性。先前未经治疗的患者的抑制剂发生率在该患者组的预期范围内。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Production of factor VIII by genetic techniques].

The human factor VIII gene and the human von Willebrand factor gene have been isolated, and were transfected into a mammalian cell line (Chinese Hamster Ovary Cells = CHO Cells). The resulting factor VIII producing cell line was thoroughly characterized. No differences were found in the recombinant factor VIII compared to plasma-derived factor VIII. For factor VIII production the cells are grown in serum-free defined medium, the recombinant factor VIII is purified by immunoaffinity chromatography plus two subsequent ion exchange steps. The absence of human raw materials for production, and a proven titer reduction of > 10(7) in the purification process significantly minimize the risk of virus transmission by the recombinant factor VIII product. Clinical studies both with previously treated and untreated patients have proven the good hemostatic efficacy and virus safety of the recombinant factor VIII. The inhibitor incidence in previously untreated patients is within the expected range for this patient group.

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