Intranasal vaccination with a plant-derived H5 HA vaccine protects mice and ferrets against highly pathogenic avian influenza virus challenge

被引:20
|
作者
Major, Diane [1 ]
Chichester, Jessica A. [2 ]
Pathirana, Rishi D. [3 ,4 ,5 ]
Guilfoyle, Kate [1 ]
Shoji, Yoko [2 ]
Guzman, Carlos A. [6 ]
Yusibov, Vidadi [2 ]
Cox, Rebecca J. [3 ,4 ,5 ]
机构
[1] Med & Healthcare Prod Regulatory Agcy, Natl Inst Biol Stand & Control, Potters Bar, Herts, England
[2] Fraunhofer USA Ctr Mol Biotechnol, Newark, DE USA
[3] Univ Bergen, Dept Clin Sci, Influenza Ctr, Bergen, Norway
[4] Haukeland Hosp, Dept Res & Dev, N-5021 Bergen, Norway
[5] Univ Bergen, KG Jebsen Ctr Influenza Vaccine Res, Bergen, Norway
[6] Helmholtz Ctr Infect Res, Dept Vaccinol & Appl Microbiol, Braunschweig, Germany
关键词
adjuvant; c-di-GMP; influenza H5N1; intranasal vaccination; ferret infection model; mice; plant vaccine; (3; 5 ')-cyclic dimeric guanylic acid; C-DI-GMP; RESPIRATORY DROPLET; MUCOSAL ADJUVANT; BELLS-PALSY; INFECTION; ANTIBODY; IMMUNOGENICITY; TRANSMISSION; RESPONSES; IMMUNITY;
D O I
10.4161/21645515.2014.988554
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Highly pathogenic avian influenza H5N1 infection remains a public health threat and vaccination is the best measure of limiting the impact of a potential pandemic. Mucosal vaccines have the advantage of eliciting immune responses at the site of viral entry, thereby preventing infection as well as further viral transmission. In this study, we assessed the protective efficacy of hemagglutinin (HA) from the A/Indonesia/05/05 (H5N1) strain of influenza virus that was produced by transient expression in plants. The plant-derived vaccine, in combination with the mucosal adjuvant (3,5)-cyclic dimeric guanylic acid (c-di-GMP) was used for intranasal immunization of mice and ferrets, before challenge with a lethal dose of the A/Indonesia/05/05 (H5N1) virus. Mice vaccinated with 15g or 5g of adjuvanted HA survived the viral challenge, while all control mice died within 10 d of challenge. Vaccinated animals elicited serum hemagglutination inhibition, IgG and IgA antibody titers. In the ferret challenge study, all animals vaccinated with the adjuvanted plant vaccine survived the lethal viral challenge, while 50% of the control animals died. In both the mouse and ferret models, the vaccinated animals were better protected from weight loss and body temperature changes associated with H5N1 infection compared with the non-vaccinated controls. Furthermore, the systemic spread of the virus was lower in the vaccinated animals compared with the controls. Results presented here suggest that the plant-produced HA-based influenza vaccine adjuvanted with c-di-GMP is a promising vaccine/adjuvant combination for the development of new mucosal influenza vaccines.
引用
收藏
页码:1235 / 1243
页数:9
相关论文
共 50 条
  • [21] Level of protection of chickens against highly pathogenic H5 avian influenza virus with Newcastle disease virus based live attenuated vector vaccine depends on homology of H5 sequence between vaccine and challenge virus
    Roemer-Oberdoerfer, Angela
    Veits, Jutta
    Helferich, Dorothee
    Mettenleiter, Thomas C.
    VACCINE, 2008, 26 (19) : 2307 - 2313
  • [22] Author Correction: Newcastle disease virus-based H5 influenza vaccine protects chickens from lethal challenge with a highly pathogenic H5N2 avian influenza virus
    Jingjiao Ma
    Jinhwa Lee
    Haixia Liu
    Ignacio Mena
    A. Sally Davis
    Sun Young Sunwoo
    Yuekun Lang
    Michael Duff
    Igor Morozov
    Yuhao Li
    Jianmei Yang
    Adolfo García-Sastre
    Juergen A. Richt
    Wenjun Ma
    npj Vaccines, 3
  • [23] Intranasal Vaccination with 1918 Influenza Virus-Like Particles Protects Mice and Ferrets from Lethal 1918 and H5N1 Influenza Virus Challenge
    Perrone, Lucy A.
    Ahmad, Attiya
    Veguilla, Vic
    Lu, Xiuhua
    Smith, Gale
    Katz, Jacqueline M.
    Pushko, Peter
    Tumpey, Terrence M.
    JOURNAL OF VIROLOGY, 2009, 83 (11) : 5726 - 5734
  • [24] Live vaccination with an H5-hemagglutinin-expressing infectious laryngotracheitis virus recombinant protects chickens against different highly pathogenic avian influenza viruses of the H5 subtype
    Pavlova, Sophia P.
    Veits, Jutta
    Mettenleiter, Thomas C.
    Fuchs, Walter
    VACCINE, 2009, 27 (37) : 5085 - 5090
  • [25] H5 cleavage-site peptide vaccine protects chickens from lethal infection by highly pathogenic H5 avian influenza viruses
    Yunyueng Jang
    Sang Heui Seo
    Archives of Virology, 2022, 167 : 67 - 75
  • [26] H5 cleavage-site peptide vaccine protects chickens from lethal infection by highly pathogenic H5 avian influenza viruses
    Jang, Yunyueng
    Seo, Sang Heui
    ARCHIVES OF VIROLOGY, 2022, 167 (01) : 67 - 75
  • [27] Newcastle disease virus-based H5 influenza vaccine protects chickens from lethal challenge with a highly pathogenic H5N2 avian influenza virus (vol 2, 33, 2017)
    Ma, Jingjiao
    Lee, Jinhwa
    Liu, Haixia
    Mena, Ignacio
    Davis, A. Sally
    Sunwoo, Sun Young
    Lang, Yuekun
    Duff, Michael
    Morozov, Igor
    Li, Yuhao
    Yang, Jianmei
    Garcia-Sastre, Adolfo
    Richt, Juergen A.
    Ma, Wenjun
    NPJ VACCINES, 2018, 3
  • [28] Protection against diverse highly pathogenic H5 avian influenza viruses in chickens immunized with a recombinant fowlpox vaccine containing an H5 avian influenza hemagglutinin gene insert
    Swayne, DE
    Garcia, M
    Beck, JR
    Kinney, N
    Suarez, DL
    VACCINE, 2000, 18 (11-12) : 1088 - 1095
  • [29] Immunological assessment of plant-derived avian flu H5/HA1 variants
    Spitsin, S.
    Andrianov, V.
    Pogrebnyak, N.
    Smirnov, Y.
    Borisjuk, N.
    Portocarrero, C.
    Veguilla, V.
    Koprowski, H.
    Golovkin, M.
    VACCINE, 2009, 27 (09) : 1289 - 1292
  • [30] Vaccine protection of chickens against antigenically diverse H5 highly pathogenic avian influenza isolates with a live HVT vector vaccine expressing the influenza hemagglutinin gene derived from a clade 2.2 avian influenza virus
    Kapczynski, Darrell R.
    Esaki, Motoyuki
    Dorsey, Kristi M.
    Jiang, Haijun
    Jackwood, Mark
    Moraes, Mauro
    Gardin, Yannick
    VACCINE, 2015, 33 (09) : 1197 - 1205