Protective efficacy of a DNA influenza virus vaccine is markedly increased by the coadministration of a Schiff base-forming drug

被引:48
作者
Charo, J
Lindencrona, JA
Carlson, LM
Hinkula, J
Kiessling, R
机构
[1] Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
[2] Karolinska Inst, Ctr Microbiol & Tumor Biol, Stockholm, Sweden
关键词
D O I
10.1128/JVI.78.20.11321-11326.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Effective vaccination against heterologous influenza virus infection remains elusive. Immunization with plasmid DNA (pDNA) expressing conserved genes from influenza virus is a promising approach to achieve cross-variant protection. However, despite having been described for more than a decade, pDNA vaccination still requires further optimization to be applied clinically as a standard vaccination approach. We have recently described a simple and efficient approach to enhance pDNA immunization, based on the use of tucaresol, a Schiff base-forming drug. In this report we have tested the ability of this drug to increase the protection conferred by pDNA vaccination against influenza virus infection. Our results demonstrate that a significant protection was achieved in two strains of mice by using the combination of pDNA and tucaresol. This protection was associated with an elevated humoral and cellular response and a switch in the type of the T helper cell (Th) immune response from type 2 to type 1. This vaccine combination represents a promising strategy for designing a clinical study for the protection from influenza and similar infections.
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页码:11321 / 11326
页数:6
相关论文
共 34 条
[1]  
Abbas A.K., 2000, CELLULAR MOL IMMUNOL
[2]   Cellular cytotoxic response induced by DNA vaccination in HIV-1-infected patients [J].
Calarota, S ;
Bratt, G ;
Nordlund, S ;
Hinkula, J ;
Leandersson, AC ;
Sandström, E ;
Wahren, B .
LANCET, 1998, 351 (9112) :1320-1325
[3]  
Charo J, 1999, J IMMUNOL, V163, P5913
[4]   Marked enhancement of the antigen-specific immune response by combining plasmid DNA-Based immunization with a Schiff base-forming drug [J].
Charo, J ;
Sundbäck, M ;
Wasserman, K ;
Ciupitu, AMT ;
Mirzai, B ;
van der Zee, R ;
Kiessling, R .
INFECTION AND IMMUNITY, 2002, 70 (12) :6652-6657
[5]  
Charo J, 2001, EUR J IMMUNOL, V31, P3602, DOI 10.1002/1521-4141(200112)31:12<3602::AID-IMMU3602>3.0.CO
[6]  
2-L
[7]   DNA immunization of HLA transgenic mice with a plasmid expressing mycobacterial heat shock protein 65 results in HLA class I- and II-restricted T cell responses that can be augmented by cytokines [J].
Charo, J ;
Sundbäck, M ;
Geluk, A ;
Ottenhoff, T ;
Kiessling, R .
HUMAN GENE THERAPY, 2001, 12 (14) :1797-1804
[8]  
Chen HQ, 1997, J IMMUNOL, V159, P2274
[9]   Active immunization in the United States: Developments over the past decade [J].
Dennehy, PH .
CLINICAL MICROBIOLOGY REVIEWS, 2001, 14 (04) :872-908
[10]  
Epstein SL, 2002, EMERG INFECT DIS, V8, P796