Protection against multiple influenza A subtypes by vaccination with highly conserved nucleoprotein

被引:240
作者
Epstein, SL [1 ]
Kong, WP
Misplon, JA
Lo, CY
Tumpey, TM
Xu, L
Nabel, GJ
机构
[1] US FDA, Ctr Biol Evaluat & Res, Div Cellular & Gene Therapies, Lab Immunol & Dev Biol, Bethesda, MD 20892 USA
[2] NIAID, Vaccine Res Ctr, NIH, Bethesda, MD 20892 USA
[3] Ctr Dis Control & Prevent, Influenza Branch, Div Viral & Rickettsial Dis, Atlanta, GA 30333 USA
关键词
influenza; DNA vaccines; adenovirus vectors; conserved antigens; animal models; H5N1; heterosubtypic immunity;
D O I
10.1016/j.vaccine.2005.04.047
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Influenza epidemic and pandemic strains cannot be predicted with certainty. Current vaccines elicit antibodies effective against specific strains, but new strategies are urgently needed for protection against unexpected strains. DNA vaccines encoding conserved antigens protect animals against diverse subtypes, but their potency needs improvement. We tested DNA prime-recombinant adenoviral boost immunization to nucleoprotein (NP). Strong antibody and T cell responses were induced. Protection against challenge was T cell-dependent and substantially more potent than DNA vaccination alone. Importantly, vaccination protected against lethal challenge with highly pathogenic H5N1 virus. Thus, gene-based vaccination with NP may contribute to protective immunity against diverse influenza viruses through its ability to stimulate cellular immunity. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5404 / 5410
页数:7
相关论文
共 35 条
  • [1] REPLICATION-DEFECTIVE ADENOVIRUS TYPE-5 AS AN IN-VITRO AND IN-VIVO GENE-TRANSFER VECTOR IN CHICKENS
    ADAM, M
    OUALIKENE, W
    LECOCQ, H
    GUITTET, M
    ELOIT, M
    [J]. JOURNAL OF GENERAL VIROLOGY, 1995, 76 : 3153 - 3157
  • [2] BIOLOGICAL AND GENETIC EVOLUTION OF THE NUCLEOPROTEIN GENE OF HUMAN INFLUENZA-A VIRUSES
    ALTMULLER, A
    FITCH, WM
    SCHOLTISSEK, C
    [J]. JOURNAL OF GENERAL VIROLOGY, 1989, 70 : 2111 - 2119
  • [3] Efficient generation of recombinant adenoviral vectors by Cre-lox recombination in vitro
    Aoki, K
    Barker, C
    Danthinne, X
    Imperiale, MJ
    Nabel, GJ
    [J]. MOLECULAR MEDICINE, 1999, 5 (04) : 224 - 231
  • [4] Heterosubtypic immunity to influenza A virus in mice lacking IgA, all Ig, NKT cells, or γδ T cells
    Benton, KA
    Misplon, JA
    Lo, CY
    Brutkiewicz, RR
    Prasad, SA
    Epstein, SL
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 166 (12) : 7437 - 7445
  • [5] Generation and evaluation of a high-growth reassortant H9N2 influenza A virus as a pandemic vaccine candidate
    Chen, HL
    Subbarao, K
    Swayne, D
    Chen, Q
    Lu, XH
    Katz, J
    Cox, N
    Matsuoka, Y
    [J]. VACCINE, 2003, 21 (17-18) : 1974 - 1979
  • [7] Dissecting the multifactorial causes of immunodominance in class I-restricted T cell responses to viruses
    Chen, WS
    Antón, LC
    Bennink, JR
    Yewdell, JW
    [J]. IMMUNITY, 2000, 12 (01) : 83 - 93
  • [8] Multiple T cell subsets control Francisella tularensis LVS intracellular growth without stimulation through macrophage interferon γ receptors
    Cowley, SC
    Elkins, KL
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (03) : 379 - 389
  • [9] RESOLUTION OF PRIMARY MURINE LISTERIOSIS AND ACQUIRED-RESISTANCE TO LETHAL SECONDARY INFECTION CAN BE MEDIATED PREDOMINANTLY BY THY-1+ CD4- CD8- CELLS
    DUNN, PL
    NORTH, RJ
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1991, 164 (05) : 869 - 877
  • [10] Vaccination with DNA encoding internal proteins of influenza virus does not require CD8+ cytotoxic T lymphocytes:: either CD4+ or CD8+ T cells can promote survival and recovery after challenge
    Epstein, SL
    Stack, A
    Misplon, JA
    Lo, CY
    Mostowski, H
    Bennink, J
    Subbarao, K
    [J]. INTERNATIONAL IMMUNOLOGY, 2000, 12 (01) : 91 - 101