UVC辐照对动物血清中病毒和支原体的有效灭活。

J Kurth, R Waldmann, J Heith, K Mausbach, R Burian
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摘要

通过动物血清传播病毒对人类和动物构成相当大的风险,特别是当血清用于生产疫苗等医药产品时。因此,适用于灭活大量不同病毒(包括包膜病毒和非包膜病毒)的程序是强制性的。为此,我们开发并验证了UVC照射作为工业环境中血清病毒灭活的首选方法。由独立的合同实验室对胎牛血清(FCS)进行了尖峰实验,结果显示,牛细小病毒、副流感III型病毒、牛腹泻病毒、口蹄疫病毒和不同形式的支原体等各种病毒的清除率一直很高。uvc处理的血清对各种细胞类型(MRC-5, Vero, CHO)保持了促进生长的活性。在10%和1% UVC处理的FCS中产生的常规生长曲线与对照组仅略有不同,这表明在UVC暴露期间没有明显的损伤。使用基于灵敏度光度法的酸性磷酸酶测定(APA)的实验,与更繁琐的细胞计数程序密切相关,即使在最低血清需求的情况下也证实了这些发现。与目前推荐的灭活方法(如伽马辐照)相比,UVC处理动物血清似乎具有优势,原因至少有三个:(i) UVC对细小病毒具有高灭活能力,而细小病毒是一种不易被常规方法破坏的病原体;(ii)它不会对细胞生长造成明显损害,(iii)它可以在生产现场以可控的方式进行。
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Efficient inactivation of viruses and mycoplasma in animal sera using UVC irradiation.

Transmission of viruses by animal sera represents a considerable risk for humans and animals particularly when the serum is used for the production of pharmaceutical products such as vaccines. Procedures applicable for inactivating large numbers of different viruses, both enveloped and non-enveloped, are therefore mandatory. For this purpose we have developed and validated UVC irradiation as the virus-inactivation procedure of choice for serum to be used in an industrial setting. Spiking experiments in foetal calf serum (FCS) were performed by independent contract laboratories and revealed constantly high clearance rates for various viruses such as bovine parvovirus, parainfluenza type III virus, bovine diarrhoea virus, foot-and-mouth disease virus and different forms of mycoplasmas. UVC-treated sera maintained their growth-promoting activities for various cell types (MRC-5, Vero, CHO). Conventional growth curves generated in the presence of 10% and 1% UVC-treated FCS differed only slightly from controls, indicating the lack of significant damage during UVC exposure. Experiments using a sensitive photometric-based acid phosphatase assay (APA), which correlates well with the more tedious cell counting procedure, confirmed these findings even in the presence of minimal serum requirements. UVC treatment of animal sera appears advantageous compared to currently recommended inactivation procedures, such as Gamma irradiation, for at least three reasons: (i) it possesses a high inactivation capacity for parvoviruses, a pathogen that cannot be destroyed easily by conventional methods; (ii) it causes no noticeable impairment in cell growth and (iii) it can be performed in a controlled manner at the production site.

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Virus removal by filtration. Gamma irradiation of bovine sera. Efficient inactivation of viruses and mycoplasma in animal sera using UVC irradiation. A universal virus inactivant for decontaminating blood and biopharmaceutical products. Serum and serum substitutes: virus safety by inactivation or removal.
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