Innate IL-10 promotes the induction of Th2 responses with plasmid DNA expressing HIV gp120

被引:36
作者
Daly, LM
Johnson, PA
Donnelly, G
Nicolson, C
Robertson, J
Mills, KHG [1 ]
机构
[1] Univ Dublin Trinity Coll, Dept Biochem, Immune Regulat Res Grp, Dublin 2, Ireland
[2] NUI Maynooth, Dept Biol, Viral Immunol Grp, Inst Immunol, Maynooth, Kildare, Ireland
[3] Natl Inst Biol Stand & Controls, Div Virol, Potters Bar, Herts, England
基金
爱尔兰科学基金会;
关键词
DNA vaccine; HIV gp120; Th1/Th2; cell;
D O I
10.1016/j.vaccine.2004.03.072
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Like most DNA vaccines, intramuscular immunization with plasmid DNA coding for influenza virus haemagglutinin (HApDNA) induced Th1 responses and IgG2a antibodies in mice. However, plasmid DNA coding for HIV gp 120 (gp120pDNA) induced Th2-biased responses and predominantly IgG1 antibodies. Responses to gp120pDNA switched to a Th1-type in IL-10-defective mice and to exclusively IgG2a antibodies in IL-4-defective mice. Conversely, antigen- specific IFN-gamma production induced by gp120pDNA or HApDNA was reduced in IL-12-defective mice, whereas addition of plasmid DNA coding for IL- 12 enhanced Th1 responses. Plasmid DNA stimulated IL- 10 and IL- 12 production by macrophages and dendritic cells (DCs) in vitro and anti-IL-10 antibodies enhanced IL- 12 production and DC maturation in response to gp120pDNA. Our findings suggest that T cell responses induced by DNA vaccines is influenced by the nature of the antigen, and that the induction of Th2-biased responses with gp120pDNA is mediated in part through the stimulation of innate IL-10, which inhibits activation of DCs that direct the induction of Th1 cells. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:963 / 974
页数:12
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