不使用单克隆抗体生产高纯度VIII因子浓缩物。

P M Mannucci, A Gringeri, M Cattaneo
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引用次数: 7

摘要

生产商正试图提高FVIII浓缩物的纯度。一些人采用的策略是包括一个纯化步骤(凝胶过滤、离子交换或亲和层析),产生中间或最终比活性为35至250 IU FVIII/mg蛋白质的浓缩物。最终产物的比活性可能较低,因为在某些浓缩物中加入了血清白蛋白以稳定FVIII。在用这些浓缩物治疗的血友病患者中,FVIII的恢复和半衰期至少与那些不太纯的浓缩物一样好。在血管性血友病患者中,这些浓缩物可增加血浆FVIII水平,但其使出血时间正常化的能力尚未得到很好的证实。他们减少的同种异体抗原负荷可能减缓人类免疫缺陷病毒(HIV)感染的进展的假设仍然没有得到证实,但是一些前瞻性研究正在试图解决这个问题。所有浓缩液都经过基于巴氏消毒或溶剂/洗涤剂处理的杀毒程序。众所周知,这些杀病毒方法和供体筛选可避免艾滋病毒传播。最近的一项大型研究表明,巴氏消毒浓缩物传播病毒性肝炎的风险很低。用溶剂/洗涤剂处理浓缩物的安全性评估是基于良好的初步结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-purity factor VIII concentrates produced without using monoclonal antibodies.

Manufacturers are attempting to increase the purity of FVIII concentrates. A strategy pursued by some is that of including a purification step (gel filtration, ion-exchange or affinity chromatography) that yields concentrates with an intermediate or final specific activity of 35 to 250 IU FVIII/mg of protein. The specific activity of the final product may be lower because serum albumin is added to some concentrates to stabilize FVIII. In hemophiliacs treated with these concentrates, FVIII recovery and half-life are at least as good as those for less pure concentrates. In patients with von Willebrand disease, these concentrates increase plasma levels of FVIII, but their capacity to normalize the bleeding time is not well established. The hypothesis that their reduced alloantigen load might slow the progression of human immunodeficiency virus (HIV) infection is still not validated, but a few prospective studies are now attempting to address this issue. All the concentrates undergo virucidal procedures based on pasteurization or treatment with solvent/detergent. It is well established that these virucidal methods and donor screening avoid HIV transmission. A recent large study has shown that a pasteurized concentrate carries a low risk of transmitting viral hepatitis. The assessment of safety from hepatitis of concentrates treated with solvent/detergent is based on favorable preliminary results.

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