Responsiveness to a pandemic alert: use of reverse genetics for rapid development of influenza vaccines

被引:199
作者
Webby, RJ
Perez, DR
Coleman, JS
Guan, Y
Knight, JH
Govorkova, EA
McClain-Moss, LR
Peiris, JS
Rehg, JE
Tuomanen, EI
Webster, RG
机构
[1] St Jude Childrens Res Hosp, Dept Infect Dis, Div Virol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Therapeut Prod & Qual, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN 38105 USA
[4] Univ Maryland, Dept Vet Med, College Pk, MD 20742 USA
[5] Univ Hong Kong, Queen Mary Hosp, Dept Pathol & Microbiol, Hong Kong, Hong Kong, Peoples R China
关键词
D O I
10.1016/S0140-6736(04)15892-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In response to the emergence of severe infection capable of rapid global spread, WHO will issue a pandemic alert. Such alerts are rare; however, on Feb 19, 2003, a pandemic alert was issued in response to human infections caused by an avian H5N1 influenza virus, A/Hong Kong/213/03. H5N1 had been noted once before in human beings in 1997 and killed a third (6/18) of infected people.(1,2) The 2003 variant seemed to have been transmitted directly from birds to human beings and caused fatal pneumonia in one of two infected individuals. Candidate vaccines were sought, but no avirulent viruses antigenically similar to the pathogen were available, and the isolate killed embryonated chicken eggs. Since traditional strategies of vaccine production were not viable, we sought to produce a candidate reference virus using reverse genetics. Methods We removed the polybasic aminoacids that are associated with high virulence from the haemagglutinin cleavage site of A/Hong Kong/213/03 using influenza reverse genetics techniques. A reference vaccine virus was then produced on an A/Puerto Rico/8/34 (PR8) backbone on WHO-approved Vero cells. We assessed this reference virus for pathogenicity in in-vivo and in-vitro assays. Findings A reference vaccine virus was produced in Good Manufacturing Practice (GMP)-grade facilities in less than 4 weeks from the time of virus isolation. This virus proved to be non-pathogenic in chickens and ferrets and was shown to be stable after multiple passages in embryonated chicken eggs. Interpretation The ability to produce a candidate reference virus in such a short period of time sets a new standard for rapid response to emerging infectious disease threats and clearly shows the usefulness of reverse genetics for influenza vaccine development. The same technologies and procedures are currently being used to create reference vaccine viruses against the 2004 H5N1 viruses circulating in Asia.
引用
收藏
页码:1099 / 1103
页数:5
相关论文
共 23 条
[1]   STRUCTURE OF THE HEMAGGLUTININ, A DETERMINANT FOR THE PATHOGENICITY OF INFLUENZA-VIRUSES [J].
BOSCH, FX ;
ORLICH, M ;
KLENK, HD ;
ROTT, R .
VIROLOGY, 1979, 95 (01) :197-207
[2]   PROTEOLYTIC CLEAVAGE OF INFLUENZA-VIRUS HEMAGGLUTININS - PRIMARY STRUCTURE OF THE CONNECTING PEPTIDE BETWEEN HA1 AND HA2 DETERMINES PROTEOLYTIC CLEAVABILITY AND PATHOGENICITY OF AVIAN INFLUENZA-VIRUSES [J].
BOSCH, FX ;
GARTEN, W ;
KLENK, HD ;
ROTT, R .
VIROLOGY, 1981, 113 (02) :725-735
[3]  
Brands R, 1999, Dev Biol Stand, V98, P93
[4]   A pandemic warning? [J].
deJong, JC ;
Claas, ECJ ;
Osterhaus, ADME ;
Webster, RG ;
Lim, WL .
NATURE, 1997, 389 (6651) :554-554
[5]   Pandemic influenza and the global vaccine supply [J].
Fedson, DS .
CLINICAL INFECTIOUS DISEASES, 2003, 36 (12) :1552-1561
[6]   Rescue of influenza A virus from recombinant DNA [J].
Fodor, E ;
Devenish, L ;
Engelhardt, OG ;
Palese, P ;
Brownlee, GG ;
García-Sastre, A .
JOURNAL OF VIROLOGY, 1999, 73 (11) :9679-9682
[7]   Avian influenza A virus (H7N7) associated with human conjunctivitis and a fatal case of acute respiratory distress syndrome. [J].
Fouchier, RAM ;
Schneeberger, PM ;
Rozendaal, FW ;
Broekman, JM ;
Kemink, SAG ;
Munstert, V ;
Kuiken, T ;
Rimmelzwaan, GF ;
Schutten, M ;
van Doornum, GJJ ;
Koch, G ;
Bosman, A ;
Koopmans, M ;
Osterhaus, ADME .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (05) :1356-1361
[8]   Safety and immunogenicity of a trivalent, inactivated, mammalian cell culture-derived influenza vaccine in healthy adults, seniors, and children [J].
Halperin, SA ;
Smith, B ;
Mabrouk, T ;
Germain, M ;
Trépanier, P ;
Hassell, T ;
Treanor, J ;
Gauthier, R ;
Mills, EL .
VACCINE, 2002, 20 (7-8) :1240-1247
[9]   A DNA transfection system for generation of influenza A virus from eight plasmids [J].
Hoffmann, E ;
Neumann, G ;
Kawaoka, Y ;
Hobom, G ;
Webster, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :6108-6113
[10]   Eight-plasmid system for rapid generation of influenza virus vaccines [J].
Hoffmann, E ;
Krauss, S ;
Perez, D ;
Webby, R ;
Webster, RG .
VACCINE, 2002, 20 (25-26) :3165-3170