Production of influenza virus in serum-free mammalian cell cultures.

O W Merten, J C Manuguerra, C Hannoun, S van der Werf
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Abstract

Human influenza viruses are routinely isolated and grown in a variety of mammalian cell substrates. However, influenza viruses for use as inactivated vaccine are still produced in embryonated eggs. Using a perfusion culture-based bioreactor process using serum-free medium, both human and equine influenza viruses of different types and subtypes could be produced to high titres. Classical DEAE-dextran microcarriers were found to be more suitable than polyester sponge carriers for virus production. In addition, MDCK cells grown in serum-free medium were further validated as the most suitable cell substrate compared to Vero and BHK-21 C13 cells for large scale virus production of influenza virus. Finally, to minimize potential contamination by adventitious agents, it was demonstrated that a new serum-free medium in which all animal-derived products are replaced by a plant extract, efficiently supports the growth of MDCK cells as well as the production of influenza virus in the presence of trypsin when using the perfusion bioreactor process.

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无血清哺乳动物细胞培养中流感病毒的产生。
人类流感病毒通常在各种哺乳动物细胞基质中分离和培养。然而,用于灭活疫苗的流感病毒仍然是在胚胎蛋中生产的。采用无血清培养基的灌注培养生物反应器工艺,可以生产出不同类型和亚型的人流感病毒和马流感病毒的高滴度。发现经典的deae -葡聚糖微载体比聚酯海绵载体更适合于病毒的产生。此外,与Vero和BHK-21 C13细胞相比,在无血清培养基中生长的MDCK细胞被进一步验证为最适合大规模生产流感病毒的细胞底物。最后,为了最大限度地减少外来因子的潜在污染,研究表明,在使用灌注生物反应器工艺时,一种新的无血清培养基中,所有动物来源的产品都被植物提取物取代,有效地支持MDCK细胞的生长以及在胰蛋白酶存在下的流感病毒的产生。
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