One-shot vaccination with an insect cell-derived low-dose influenza A H7 virus-like particle preparation protects mice against H7N9 challenge

被引:63
作者
Klausberger, Miriam [1 ]
Wilde, Monika [1 ]
Palmberger, Dieter [1 ]
Hai, Rong [2 ]
Albrecht, Randy A. [2 ,3 ]
Margine, Irina [2 ,4 ]
Hirsh, Ariana [2 ]
Garcia-Sastre, Adolfo [2 ,3 ,5 ]
Grabherr, Reingard [1 ]
Krammer, Florian [2 ]
机构
[1] Univ Nat Resources & Life Sci, Vienna Inst BioTechnol, Vienna, Austria
[2] Icahn Sch Med Mt Sinai, Dept Microbiol, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Global Hlth & Emerging Pathogens Inst, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Grad Sch Biol Sci, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Div Infect Dis, Dept Med, New York, NY 10029 USA
基金
奥地利科学基金会;
关键词
Influenza; H7N9; Pandemic; Virus-like particle; Baculovirus; Cross-reactivity; IMMUNE-RESPONSE; HUMAN INFECTION; T-CELLS; HEMAGGLUTININ; GENERATION; PATHOGENICITY; ANTIBODIES; CANDIDATE; VACCINES; ORIGIN;
D O I
10.1016/j.vaccine.2013.11.036
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human infections with a novel influenza A H7N9 subtype virus were reported in China recently. The virus caused severe disease with high mortality rates and it raised concerns over its pandemic potential. Here, we assessed in the mouse model protective efficacy of single immunisations with low vaccine doses of insect cell-derived H7 virus-like particles, consisting of hemagglutinin and matrix protein. Vaccinated mice were fully protected and survived a stringent lethal challenge (100 mLD50) with H7N9, even after a single, unadjuvanted, low vaccine dose (0.03 mu.g). Serum analysis revealed broad reactivity and hemagglutination inhibition activity across a panel of divergent H7 strains. Moreover, we detected significant levels of cross-reactivity to related group 2 hemagglutinins. These data demonstrate that virus-like particle vaccines have the potential to induce broadly protective immunity against the novel H7N9 virus and a variety of other H7 strains. (C) 2013 The Author. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:355 / 362
页数:8
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