Intranasal immunization with H5N1 vaccine plus Poly I:Poly C12U, a Toll-like receptor agonist, protects mice against homologous and heterologous virus challenge

被引:74
作者
Ichinohe, Takeshi
Kawaguchi, Akira
Tamura, Shin-ichi
Takahashi, Hidehiro
Sawa, Hirofumi
Ninomiya, Ai
Imai, Masaki
Itamura, Shigeyuki
Odagiri, Takato
Tashiro, Masato
Chiba, Joe
Sata, Tetsutaro
Kurata, Takeshi
Hasegawa, Hideki
机构
[1] Natl Inst Infect Dis, Dept Pathol, Tokyo 2080011, Japan
[2] Tokyo Univ Sci, Dept Biol Sci & Technol, Chiba 2788510, Japan
[3] Natl Inst Infect Dis, Dept Virol 3, Tokyo 2080011, Japan
[4] Hokkaido Univ, Res Ctr Zoonosis Control, 21st Century COE Program Zoonosis Control, Dept Mol Pathol,Kita Ku, Sapporo, Hokkaido 0600818, Japan
关键词
influenza virus; H5N1; subtype; ampligen; adjuvant; immunoglobulin A;
D O I
10.1016/j.micinf.2007.06.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The avian H5N1 influenza virus has the potential to cause a new pandemic. Since it is difficult to predict which strain of influenza will cause a pandemic, it is advantageous to produce vaccines that confer cross-protective immunity. Mucosal vaccine administration was reported to induce cross-protective immunity by inducing secretion of IgA at the mucosal surface. Adjuvants can also enhance the development of fully protective mucosal immunity. Here we show that a new mucosal adjuvant, polyI:polyC(12)U (Ampligen (R)), a Toll-like receptor 3 agonist proven to be safe in a Phase III human trial, is an effective adjuvant for H5N1 influenza vaccination. Intranasal administration of a candidate influenza vaccine with Ampligen resulted in secretion of IgA, and protected mice that were subsequently challenged with homologous A/Vietnam/1194/2004 and heterologous A/HK/483/97 and A/Indonesia/6/2005 virus. (C) 2007 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1333 / 1340
页数:8
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