Benton C V, Hodge H M, Fine D L
In Vitro. 1978 Feb;14(2):192-9. doi: 10.1007/BF02618222.
A cell culture method is described for the large-scale (50 to 150 1) production of Mason-Pfizer monkey virus and squirrel monkey virus, two primate retroviruses. Virus production was achieved with suspension cultures of chronically infected A204 human rhabdomyosarcoma cells harvested and clarified in the logarithmic stages of cell culture growth. Methods for the subsequent purification and concentration of virus material utilizing zonal centrifugation also are described. Applications of these methodologies resulted in products that afforded biochemical comparisons of these agents in a manner such that host cell-derived variations were minimized. These data indicated that high levels of production and efficient recovery and purification of virus material were achieved.
描述了一种细胞培养方法,用于大规模(50至150升)生产两种灵长类逆转录病毒——梅森- Pfizer猴病毒和松鼠猴病毒。通过对慢性感染的A204人横纹肌肉瘤细胞进行悬浮培养来实现病毒生产,这些细胞在细胞培养生长的对数期收获并澄清。还描述了利用区带离心对病毒材料进行后续纯化和浓缩的方法。这些方法的应用产生了能够以最小化宿主细胞衍生变异的方式对这些病原体进行生化比较的产品。这些数据表明,实现了病毒材料的高水平生产以及高效回收和纯化。