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Performance characteristics of qualified cell lines for isolation and propagation of influenza viruses for vaccine manufacturing

机译:用于疫苗生产的流感病毒分离和繁殖的合格细胞系的性能特征

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摘要

Cell culture is now available as a method for the production of influenza vaccines in addition to eggs. In accordance with currently accepted practice, viruses recommended as candidates for vaccine manufacture are isolated and propagated exclusively in hens' eggs prior to distribution to manufacturers. Candidate vaccine viruses isolated in cell culture are not available to support vaccine manufacturing in mammalian cell bioreactors so egg-derived viruses have to be used. Recently influenza A (H3N2) viruses have been difficult to isolate directly in eggs. As mitigation against this difficulty, and the possibility of no suitable egg-isolated candidate viruses being available, it is proposed to consider using mammalian cell lines for primary isolation of influenza viruses as candidates for vaccine production in egg and cell platforms.To investigate this possibility, we tested the antigenic stability of viruses isolated and propagated in cell lines qualified for influenza vaccine manufacture and subsequently investigated antigen yields of such viruses in these cell lines at pilot-scale. Twenty influenza A and B-positive, original clinical specimens were inoculated in three MDCK cell lines. The antigenicity of recovered viruses was tested by hemagglutination inhibition using ferret sera against contemporary vaccine viruses and the amino acid sequences of the hemagglutinin and neuraminidase were determined. MDCK cell lines proved to be highly sensitive for virus isolation. Compared to the virus sequenced from the original specimen, viruses passaged three times in the MDCK lines showed up to 2 amino acid changes in the hemagglutinin. Antigenic stability was also established by hemagglutination inhibition titers comparable to those of the corresponding reference virus. Viruses isolated in any of the three MDCK lines grew reasonably well but variably in three MDCK cells and in VERO cells at pilot-scale. These results indicate that influenza viruses isolated in vaccine certified cell lines may well qualify for use in vaccine production.
机译:现在,细胞培养可用作除蛋之外的流感疫苗生产方法。根据当前公认的惯例,在分配给制造商之前,将被推荐作为疫苗生产候选物的病毒被分离并专门在母鸡卵中繁殖。在细胞培养物中分离出的候选疫苗病毒无法支持在哺乳动物细胞生物反应器中生产疫苗,因此必须使用鸡蛋衍生的病毒。最近,很难在鸡蛋中直接分离出甲型H3N2流感病毒。为了缓解这种困难以及没有合适的鸡蛋分离候选病毒的可能性,建议考虑使用哺乳动物细胞系初步分离流感病毒作为在鸡蛋和细胞平台上生产疫苗的候选药物。 ,我们测试了在合格的流感疫苗生产细胞系中分离和繁殖的病毒的抗原稳定性,并随后在中试规模下研究了这些病毒在这些细胞系中的抗原产量。将二十种甲型和乙型流感阳性的原始临床标本接种到三种MDCK细胞系中。通过使用白鼬血清对当代疫苗病毒的血凝抑制作用来测试回收的病毒的抗原性,并测定血凝素和神经氨酸酶的氨基酸序列。事实证明,MDCK细胞系对病毒分离高度敏感。与从原始标本测序的病毒相比,在MDCK系中传代3次的病毒在血凝素中最多显示2个氨基酸变化。还通过与相应参考病毒相当的血凝抑制效价建立了抗原稳定性。在三个MDCK系中的任何一个中分离出的病毒均生长良好,但在三个MDCK细胞和VERO细胞中处于中试规模。这些结果表明,在疫苗认证的细胞系中分离出的流感病毒很可能适合用于疫苗生产。

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