Sensitization with vaccinia virus encoding H5N1 hemagglutinin restores immune potential against H5N1 influenza virus

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作者
Fumihiko Yasui
Yasushi Itoh
Ai Ikejiri
Masahiro Kitabatake
Nobuo Sakaguchi
Keisuke Munekata
Shintaro Shichinohe
Yukiko Hayashi
Hirohito Ishigaki
Misako Nakayama
Yoshihiro Sakoda
Hiroshi Kida
Kazumasa Ogasawara
Michinori Kohara
机构
[1] Tokyo Metropolitan Institute of Medical Science,Department of Microbiology and Cell Biology
[2] Shiga University of Medical Science,Division of Pathology and Disease Regulation, Department of Pathology
[3] Setatsukinowa,Department of Immunology
[4] Nara Medical University,Department of Disease Control
[5] WPI Immunology Frontier Research Center,undefined
[6] Osaka University,undefined
[7] Laboratory of Microbiology,undefined
[8] Graduate School of Veterinary Medicine,undefined
[9] Hokkaido University,undefined
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摘要
H5N1 highly pathogenic avian influenza (H5N1 HPAI) virus causes elevated mortality compared with seasonal influenza viruses like H1N1 pandemic influenza (H1N1 pdm) virus. We identified a mechanism associated with the severe symptoms seen with H5N1 HPAI virus infection. H5N1 HPAI virus infection induced a decrease of dendritic cell number in the splenic extrafollicular T-cell zone and impaired formation of the outer layers of B-cell follicles, resulting in insufficient levels of antibody production after infection. However, in animals vaccinated with a live recombinant vaccinia virus expressing the H5 hemagglutinin, infection with H5N1 HPAI virus induced parafollicular dendritic cell accumulation and efficient antibody production. These results indicate that a recombinant vaccinia encoding H5 hemagglutinin gene does not impair dendritic cell recruitment and can be a useful vaccine candidate.
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