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一种用于净化血液和生物制药产品的通用病毒灭活剂。

A universal virus inactivant for decontaminating blood and biopharmaceutical products.

作者信息

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

机构信息

Plum Island Animal Disease Center, Greenport, NY 11944, USA.

出版信息

Dev Biol Stand. 1999;99:119-30.

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.

摘要

从血液以及由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能受到损害。对于血液、未分级的血浆或血清而言,这个问题更具挑战性。基因组的选择性失活是制备灭活病毒疫苗的关键步骤。亚胺已被用于制备灭活口蹄疫病毒疫苗30多年,没有任何病毒感染性存活的证据。此外,病毒的免疫原性未受损害。所有公认病毒科的病毒都可被亚胺灭活。使用能确保灭活>10(15)个脊髓灰质炎病毒和口蹄疫病毒(FMDV)感染单位的条件时,包括小牛血清中促进细胞生长因子在内的几种蛋白质的生物学特性不会受到损害。此外,两种病毒都可在4℃被亚胺灭活,从而提供了一种从在较高温度下不稳定的蛋白质制剂中去除感染性的方法。已经研究了FMDV被灭活的机制。我们发现,在4℃灭活后从病毒中提取的RNA没有降解,也没有隐藏的断裂,但仍然没有感染性。然而,使用对应于编码病毒RNA聚合酶一部分的基因的引物,它可以通过PCR扩增,但不能从编码结构蛋白之一VP1的基因扩增,这表明该区域发生了一个或多个碱基的改变。

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