A universal virus inactivant for decontaminating blood and biopharmaceutical products.

F Brown, R F Meyer, M Law, E Kramer, J F Newman
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Abstract

Removal of virus infectivity from blood and biopharmaceutical products prepared from blood is an issue of considerable importance. Irrespective of the methods that are chosen it is vital that the biological activity of the product is not impaired. For blood and unfractionated plasma or serum, the problem is even more challenging. Selective inactivation of the genome is the key step in the preparation of killed virus vaccines. Imines have been used for more than 30 years for the preparation of inactivated foot-and-mouth disease virus vaccines without any evidence of survival of virus infectivity. Moreover, the immunogenicity of the virus is unimpaired. Viruses belonging to all the recognised families can be inactivated by imines. The biological properties of several proteins, including the cell growth-promoting factors in calf serum, are not impaired using conditions which ensure the inactivation of > 10(15) infectious units of poliovirus and foot-and-mouth disease virus (FMDV). Moreover, both viruses can be inactivated by imines at 4 degrees C, thus providing a method for removing infectivity from protein preparations which are unstable at higher temperatures. The mechanism by which FMDV is inactivated has been studied. We found that the RNA extracted from the virus after inactivation at 4 degrees C was not degraded and contained no hidden breaks but nevertheless was non-infectious. However, it could be amplified by PCR using primers corresponding to the gene coding for a portion of the viral RNA polymerase, but not from that coding for VP1, one of the structural proteins, showing that alteration of a base or bases had occurred in that region.

用于净化血液和生物制药产品的通用病毒灭活剂。
从血液和从血液制备的生物制药产品中去除病毒感染性是一个相当重要的问题。无论选择何种方法,至关重要的是产品的生物活性不受损害。对于血液和未分离的血浆或血清,问题甚至更具挑战性。基因组的选择性失活是制备灭活病毒疫苗的关键步骤。30多年来,亚胺一直用于制备灭活的口蹄疫病毒疫苗,没有任何证据表明病毒传染性存活。此外,病毒的免疫原性没有受损。属于所有已知科的病毒都可以被亚胺灭活。在确保脊髓灰质炎病毒和口蹄疫病毒(FMDV)≥10(15)个感染单位灭活的条件下,几种蛋白质的生物学特性,包括小牛血清中的细胞生长促进因子,不会受到损害。此外,这两种病毒都可以在4摄氏度时被亚胺灭活,从而提供了一种在较高温度下不稳定的蛋白质制剂中去除感染性的方法。研究了FMDV灭活的机制。我们发现,从4℃灭活后的病毒中提取的RNA没有被降解,也没有隐藏的断裂,但仍然是非传染性的。然而,它可以用与编码病毒RNA聚合酶部分基因对应的引物进行PCR扩增,但不能从编码结构蛋白之一VP1的引物中扩增,这表明该区域发生了一个或多个碱基的改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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