Performance characteristics of qualified cell lines for isolation and propagation of influenza viruses for vaccine manufacturing
Web of Science
AuthorDonis, RO; Chen, I-M; Davis, CT; Foust, A; Hossain, MJ; Johnson, A; Klimov, A; Loughlin, R; Xu, X; Tsai, T; ...
PublisherELSEVIER SCI LTD
University of Melbourne Author/sBarr, Ian
AffiliationMicrobiology and Immunology
Document TypeJournal Article
CitationsDonis, R. O., Chen, I. -M., Davis, C. T., Foust, A., Hossain, M. J., Johnson, A., Klimov, A., Loughlin, R., Xu, X., Tsai, T., Blayer, S., Trusheim, H., Colegate, T., Fox, J., Taylor, B., Hussain, A., Barr, I., Baas, C., Louwerens, J. ,... Ziegler, T. (2014). Performance characteristics of qualified cell lines for isolation and propagation of influenza viruses for vaccine manufacturing. VACCINE, 32 (48), pp.6583-6590. https://doi.org/10.1016/j.vaccine.2014.06.045.
Access StatusOpen Access
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.
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