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
相关论文
共 30 条
[11]   Toll-like receptor control of the adaptive immune responses [J].
Iwasaki, A ;
Medzhitov, R .
NATURE IMMUNOLOGY, 2004, 5 (10) :987-995
[12]   BIOLOGICAL-ACTIVITY OF MONOCLONAL-ANTIBODIES TO OPERATIONALLY DEFINED ANTIGENIC REGIONS ON THE HEMAGGLUTININ MOLECULE OF A/SEAL MASSACHUSETTS/1/80 (H7N7) INFLUENZA-VIRUS [J].
KIDA, H ;
BROWN, LE ;
WEBSTER, RG .
VIROLOGY, 1982, 122 (01) :38-47
[13]   CROSS-PROTECTION IN MICE INFECTED WITH INFLUENZA-A VIRUS BY THE RESPIRATORY ROUTE IS CORRELATED WITH LOCAL IGA ANTIBODY RATHER THAN SERUM ANTIBODY OR CYTO-TOXIC T-CELL REACTIVITY [J].
LIEW, FY ;
RUSSELL, SM ;
APPLEYARD, G ;
BRAND, CM ;
BEALE, J .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1984, 14 (04) :350-356
[14]   Efficacy of H5 influenza vaccines produced by reverse genetics in a lethal mouse model [J].
Lipatov, AS ;
Webby, RJ ;
Govorkova, EA ;
Krauss, S ;
Webster, RG .
JOURNAL OF INFECTIOUS DISEASES, 2005, 191 (08) :1216-1220
[15]   Th1-specific cell surface protein Tim-3 regulates macrophage activation and severity of an autoimmune disease [J].
Monney, L ;
Sabatos, CA ;
Gaglia, JL ;
Ryu, A ;
Waldner, H ;
Chernova, T ;
Manning, S ;
Greenfield, EA ;
Coyle, AJ ;
Sobel, RA ;
Freeman, GJ ;
Kuchroo, VK .
NATURE, 2002, 415 (6871) :536-541
[16]  
Mutsch M, 2004, NEW ENGL J MED, V350, P896, DOI 10.1056/NEJMoa030595
[17]   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
[18]   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
[19]   PHASE 1-2 TRIAL OF MULTIPLE-DOSE POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID IN PATIENTS WITH LEUKEMIA OR SOLID TUMORS [J].
ROBINSON, RA ;
DEVITA, VT ;
LEVY, HB ;
BARON, S ;
HUBBARD, SP ;
LEVINE, AS .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1976, 57 (03) :599-602
[20]   Nasal immunization with anthrax protective antigen protein adjuvanted with polyriboinosinic-polyribocytidylic acid induced strong mucosal and systemic immunities [J].
Sloat, Brian R. ;
Cui, Zhengrong .
PHARMACEUTICAL RESEARCH, 2006, 23 (06) :1217-1226