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Publication Date:
March 2008
ISSN:
1437-4315
DOI:
10.1515/BC.2008.060

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Editor-in-Chief: Brüne, Bernhard

Editorial Board Member: Ludwig, Stephan / Sies, Helmut / Stoffel, Markus / Turk, Boris / Wittinghofer, Alfred / Baumeister, Wolfgang / Bergeron, John / Bogyo, Matthew / Bürkle, Alexander / Cadenas, Enrique / Chiti, Fabrizio / Dikic, Ivan / Dobson, Christopher / Driessen, Arnold / Fritz, Hans / Gevaert, Kris / Hammann, Christian / Hartl, F. Ulrich / Häussinger, Dieter / Hiscott, John / Igarashi, Yasuyuki / Klotz, Lars-Oliver / Krüger, Achim / Magdolen, Viktor / Müschen, Markus / Narumiya, Shuh / Naumann, Michael / Pejler, Gunnar / Pfanner, Nikolaus / Pike, Robert / Potempa, Jan / Saftig, Paul / Sandhoff, Konrad / Schaffner, Walter / Sinning, Irmgard / Sommerhoff, Christian P.

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Pre-clinical development of cell culture (Vero)-derived H5N1 pandemic vaccines

M. Keith Howard1 / Otfried Kistner2 / P. Noel Barrett3

1Baxter AG, Biomedical Research Centre, Uferstrasse 15, A-2304 Orth/Donau, Austria

2Baxter AG, Biomedical Research Centre, Uferstrasse 15, A-2304 Orth/Donau, Austria

3Baxter AG, Biomedical Research Centre, Uferstrasse 15, A-2304 Orth/Donau, Austria

Corresponding author

Citation Information: Biological Chemistry. Volume 389, Issue 5, Pages 569–577, ISSN (Online) 14374315, ISSN (Print) 1431-6730, DOI: 10.1515/BC.2008.060, March 2008

Publication History:
Received:
2007-10-17
Accepted:
2008-01-29
Published Online:
2008-03-27

Abstract

The rapid spread of avian influenza (H5N1) and its transmission to humans has raised the possibility of an imminent pandemic and concerns over the ability of standard influenza vaccine production methods to 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, produced at a variety of manufacturing scales, were demonstrated to be highly immunogenic in animal models without the need for adjuvant. The vaccines induce cross-neutralising antibodies and are protective in a mouse challenge model not only against the homologous virus but against other H5N1 strains, including those from other clades. 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.

Keywords: cross-protection; influenza virus; Vero cells; whole virus vaccine

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