| Literature DB >> 17614165 |
Otfried Kistner1, M Keith Howard, Martin Spruth, Walter Wodal, Peter Brühl, Marijan Gerencer, Brian A Crowe, Helga Savidis-Dacho, Ian Livey, Manfred Reiter, Ines Mayerhofer, Christa Tauer, Leopold Grillberger, Wolfgang Mundt, Falko G Falkner, P Noel Barrett.
Abstract
The rapid spread and the transmission to humans of avian influenza virus (H5N1) have induced world-wide fears of a new pandemic and raised concerns over the ability of standard influenza vaccine production methods to rapidly supply sufficient amounts of an effective vaccine. We report here on a robust and flexible strategy which uses wild-type virus grown in a continuous cell culture (Vero) system to produce an inactivated whole virus vaccine. Candidate vaccines based on clade 1 and clade 2 influenza H5N1 strains were developed and demonstrated to be highly immunogenic in animal models. The vaccines induce cross-neutralising antibodies, highly cross-reactive T-cell responses and are protective in a mouse challenge model not only against the homologous virus but also against other H5N1 strains, including those from another clade. These data indicate that cell culture-grown whole virus vaccines, based on the wild-type virus, allow the rapid high yield production of a candidate pandemic vaccine.Entities:
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Year: 2007 PMID: 17614165 PMCID: PMC2040225 DOI: 10.1016/j.vaccine.2007.05.013
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641