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

被引:30
作者
Howard, M. Keith [1 ]
Kistner, Offried [1 ]
Barrett, P. Noel [1 ]
机构
[1] Baxter AG, Biomed Res Ctr, A-2304 Orth, Austria
关键词
cross-protection; influenza virus; Vero cells; whole virus vaccine;
D O I
10.1515/BC.2008.060
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 wildtype virus, allow the rapid high-yield production of a candidate pandemic vaccine.
引用
收藏
页码:569 / 577
页数:9
相关论文
共 35 条
[1]  
Aubin JT, 2005, EMERG INFECT DIS, V11, P1515
[2]   Safety and immunogenicity of an inactivated split-virion influenza A/Vietnam/1194/2004 (H5N1) vaccine:: phase I randomised trial [J].
Bresson, Jean-Louis ;
Perronne, Christian ;
Launay, Odile ;
Gerdil, Catherine ;
Saville, Melanie ;
Wood, John ;
Hoeschler, Katja ;
Zambon, Maria C. .
LANCET, 2006, 367 (9523) :1657-1664
[3]   Wave microcarrier cultivation of MDCK cells for influenza virus production in serum containing and serum-free media [J].
Genzel, Y. ;
Olmer, R. M. ;
Schafer, B. ;
Reichl, U. .
VACCINE, 2006, 24 (35-36) :6074-6087
[4]   African green monkey kidney (Vero) cells provide an alternative host cell system for influenza A and B viruses [J].
Govorkova, EA ;
Murti, G ;
Meignier, B ;
deTaisne, C ;
Webster, RG .
JOURNAL OF VIROLOGY, 1996, 70 (08) :5519-5524
[5]   Immunization with reverse-genetics-produced H5N1 influenza vaccine protects ferrets against homologous and heterologous challenge [J].
Govorkova, Elena A. ;
Webby, Richard J. ;
Humberd, Jennifer ;
Seiler, Jon P. ;
Webster, Robert G. .
JOURNAL OF INFECTIOUS DISEASES, 2006, 194 (02) :159-167
[6]   H5N1 influenza: A protean pandemic threat [J].
Guan, Y ;
Poon, LLM ;
Cheung, CY ;
Ellis, TM ;
Lim, W ;
Lipatov, AS ;
Chan, KH ;
Sturm-Ramirez, KM ;
Cheung, CL ;
Leung, YHC ;
Yuen, KY ;
Webster, RG ;
Peiris, JSM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (21) :8156-8161
[7]   EGG FLUIDS AND CELLS OF THE CHORIOALLANTOIC MEMBRANE OF EMBRYONATED CHICKEN EGGS CAN SELECT DIFFERENT VARIANTS OF INFLUENZA-A (H3N2) VIRUSES [J].
HARDY, CT ;
YOUNG, SA ;
WEBSTER, RG ;
NAEVE, CW ;
OWENS, RJ .
VIROLOGY, 1995, 211 (01) :302-306
[8]   Antigenic differences between H5N1 human influenza viruses isolated in 1997 and 2003 [J].
Horimoto, T ;
Fukuda, N ;
Iwatsuki-Horimoto, K ;
Guan, Y ;
Lim, W ;
Peiris, M ;
Sugii, S ;
Odagiri, T ;
Tashiro, M ;
Kawaoka, Y .
JOURNAL OF VETERINARY MEDICAL SCIENCE, 2004, 66 (03) :303-305
[9]   Haemagglutinin quantification and identification of influenza A&B strains propagated in PER.C6® cells:: A novel RP-HPLC method [J].
Kapteyn, JC ;
Saidi, MD ;
Dijkstra, R ;
Kars, C ;
Tjon, JCMSK ;
Weverling, GJ ;
de Vocht, ML ;
Kompier, R ;
van Montfort, BA ;
Guichoux, JY ;
Goudsmit, J ;
Lagerwerf, FM .
VACCINE, 2006, 24 (16) :3137-3144
[10]   EFFICACY OF INACTIVATED INFLUENZA-A VIRUS (H3N2) VACCINES GROWN IN MAMMALIAN-CELLS OR EMBRYONATED EGGS [J].
KATZ, JM ;
WEBSTER, RG .
JOURNAL OF INFECTIOUS DISEASES, 1989, 160 (02) :191-199