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首个源自人类的重组人凝血因子 VIII:人细胞系和生产特征。

The first recombinant human coagulation factor VIII of human origin: human cell line and manufacturing characteristics.

机构信息

Octapharma, Munich, Germany.

出版信息

Eur J Haematol. 2012 Aug;89(2):165-76. doi: 10.1111/j.1600-0609.2012.01804.x. Epub 2012 Jun 15.

DOI:10.1111/j.1600-0609.2012.01804.x
PMID:22690791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3443369/
Abstract

INTRODUCTION

Since the early 1990s, recombinant human clotting factor VIII (rhFVIII) produced in hamster cells has been available for haemophilia A treatment. However, the post-translational modifications of these proteins are not identical to those of native human FVIII, which may lead to immunogenic reactions and the development of inhibitors against rhFVIII. For the first time, rhFVIII produced in a human host cell line is available.

AIM

We describe here the establishment of the first human production cell line for rhFVIII and the manufacturing process of this novel product.

METHODS AND RESULTS

A human cell line expressing rhFVIII was derived from human embryonic kidney (HEK) 293 F cells transfected with an FVIII expression plasmid. No virus or virus-like particles could be detected following extensive testing. The stringently controlled production process is completely free from added materials of animal or human origin. Multistep purification employing a combination of filtration and chromatography steps ensures the efficient removal of impurities. Solvent/detergent treatment and a 20 nm pore size nanofiltration step, used for the first time in rhFVIII manufacturing, efficiently eliminate any hypothetically present viruses. In contrast to hamster cell-derived products, this rhFVIII product does not contain hamster-like epitopes, which might be expected to be immunogenic.

CONCLUSIONS

HEK 293 F cells, whose parental cell line HEK 293 has been used by researchers for decades, are a suitable production cell line for rhFVIII and will help avoid immunogenic epitopes. A modern manufacturing process has been developed to ensure the highest level of purity and pathogen safety.

摘要

简介

自 20 世纪 90 年代初以来,仓鼠细胞生产的重组人凝血因子 VIII(rhFVIII)已被用于治疗甲型血友病。然而,这些蛋白质的翻译后修饰与天然人 FVIII 并不完全相同,这可能导致免疫反应和针对 rhFVIII 的抑制剂的产生。现在,首次可以获得在人宿主细胞系中生产的 rhFVIII。

目的

我们在此描述了第一个 rhFVIII 人生产细胞系的建立以及该新型产品的制造工艺。

方法和结果

通过转染含有 FVIII 表达质粒的人胚肾(HEK)293 F 细胞,获得了表达 rhFVIII 的人细胞系。经过广泛的测试,未检测到病毒或类病毒颗粒。严格控制的生产过程完全不含动物或人源的添加材料。采用过滤和色谱步骤的多步纯化可有效去除杂质。溶剂/去污剂处理和 20nm 孔径纳米过滤步骤,首次用于 rhFVIII 生产,可有效去除任何潜在的存在的病毒。与仓鼠细胞衍生产品不同,该 rhFVIII 产品不含可能具有免疫原性的类仓鼠表位。

结论

HEK 293 F 细胞的亲本细胞系 HEK 293 已被研究人员使用了几十年,是 rhFVIII 的合适生产细胞系,并将有助于避免免疫原性表位。已经开发出一种现代制造工艺,以确保最高水平的纯度和病原体安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/f153a9e16049/ejh0089-0165-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/611f60fbeff4/ejh0089-0165-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/b5544a95f8f4/ejh0089-0165-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/25910fac7039/ejh0089-0165-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/01feeab222ce/ejh0089-0165-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/f153a9e16049/ejh0089-0165-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/611f60fbeff4/ejh0089-0165-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/b5544a95f8f4/ejh0089-0165-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/25910fac7039/ejh0089-0165-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/01feeab222ce/ejh0089-0165-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79be/3443369/f153a9e16049/ejh0089-0165-f5.jpg

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