Developing Vaccines to Combat Pandemic Influenza

被引:18
作者
Robertson, James S. [1 ]
Engelhardt, Othmar G. [1 ]
机构
[1] Natl Inst Biol Stand & Controls, Div Virol, Hlth Protect Agcy, Potters Bar EN6 3QG, Herts, England
来源
VIRUSES-BASEL | 2010年 / 2卷 / 02期
基金
英国医学研究理事会;
关键词
pandemic influenza vaccines; reverse genetics; H5N1; virus; H1N1v virus; REVERSE GENETICS SYSTEM; A VIRUS GENERATION; AVIAN INFLUENZA; H5N1; INFLUENZA; HEMAGGLUTININ CLEAVAGE; RANDOMIZED-TRIAL; STRAINS; GENOME; GROWTH; SAFETY;
D O I
10.3390/v2020532
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Influenza vaccine manufacturers require antigenically relevant vaccine viruses that have good manufacturing properties and are safe to use. In developing pandemic vaccine viruses, reverse genetics has been employed as a rational approach that can also be used effectively to attenuate the highly virulent H5N1 virus and at the same time place the H5 HA and N1 NA on a background of PR8, a virus that has been used over many decades to provide high yielding vaccine viruses. Reverse genetics has also been used successfully alongside classical reassorting techniques in the development of (swine flu) pandemic A(H1N1) v vaccine viruses.
引用
收藏
页码:532 / 546
页数:15
相关论文
共 51 条
[21]   Antigen sparing and cross-reactive immunity with an adjuvanted rH5N1 prototype pandemic influenza vaccine:: a randomised controlled trial [J].
Leroux-Roels, Isabel ;
Borkowski, Astrid ;
Vanwolleghem, Thomas ;
Drame, Mamadou ;
Clement, Frederic ;
Hons, Eliane ;
Devaster, Jeanne-Marie ;
Leroux-Roels, Geert .
LANCET, 2007, 370 (9587) :580-589
[22]   INFLUENZA-VIRUS GENOME CONSISTS OF 8 DISTINCT RNA SPECIES [J].
MCGEOCH, D ;
FELLNER, P ;
NEWTON, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (09) :3045-3049
[23]   An improved reverse genetics system for influenza A virus generation and its implications for vaccine production [J].
Neumann, G ;
Fujii, K ;
Kino, Y ;
Kawaoka, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (46) :16825-16829
[24]   Generation of influenza A viruses entirely from cloned cDNAs [J].
Neumann, G ;
Watanabe, T ;
Ito, H ;
Watanabe, S ;
Goto, H ;
Gao, P ;
Hughes, M ;
Perez, DR ;
Donis, R ;
Hoffmann, E ;
Hobom, G ;
Kawaoka, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9345-9350
[25]  
*NIBSC HPA, CURR AV NIBSC CAND I
[26]   Safety and antigenicity of non-adjuvanted and MF59-adjuvanted influenza A/Duck/Singapore/97 (H5N3) vaccine: a randomised trial of two potential vaccines against H5N1 influenza [J].
Nicholson, KG ;
Colegate, AE ;
Podda, A ;
Stephenson, I ;
Wood, J ;
Ypma, E ;
Zambon, MC .
LANCET, 2001, 357 (9272) :1937-1943
[27]   Generation of influenza vaccine viruses on Vero cells by reverse genetics: an H5N1 candidate vaccine strain produced under a quality system [J].
Nicolson, C ;
Major, D ;
Wood, JA ;
Robertson, JS .
VACCINE, 2005, 23 (22) :2943-2952
[28]  
*OIE AV INFL, 2009, MAN DIAGN TESTS VACC
[29]   An adenovirus vector-mediated reverse genetics system for influenza A virus generation [J].
Ozawa, Makoto ;
Goto, Hideo ;
Horimoto, Taisuke ;
Kawaoka, Yoshihiro .
JOURNAL OF VIROLOGY, 2007, 81 (17) :9556-9559
[30]  
QIU YZ, INFLUENZA OTHER RESP, V2, P237