Generation of Th1 immune responses to inactivated, gp120-depleted HIV-1 in mice with a dominant Th2 biased immune profile via imunostimulatory oligonucleotides - relevance to AIDS vaccines in developing countries

被引:18
作者
Ayash-Rashkovsky, M
Weisman, Z
Diveley, J
Moss, RB
Bentwich, Z [1 ]
Borkow, G
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Ruth Ben Ari Inst Clin Immunol, IL-76100 Rehovot, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Sch, AIDS Ctr, Kaplan Med Ctr, IL-76100 Rehovot, Israel
[3] Immune Response Corp, Carlsbad, CA 92008 USA
关键词
CpG ODN; Th1 and Th2 cytokine profile; HIV-1; immunogen; Schistosoma;
D O I
10.1016/S0264-410X(02)00202-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vaccination against HIV-1 of hosts with a dominant Th2 immune profile may fail to induce essential protective Th1 immune responses. By using Schistosoma-infected mice, with a pre-existent Th2 immune background, we demonstrate that oligodeoxynucleotides (ODN) containing unmethylated cytosine-phosphate-guano sine (CpG) immunostimulatory sequences co-administered with inactivated, gp120-depleted HIV-1 viral particles (HIV-1 immunogen) lead to potent Th1 anti-HIV-1 immune responses overcoming the Th2 bias. In contrast, Schistosoma-infected mice immunized with HIV-1 immunogen in incomplete Freund's adjuvant only, induced Th2 anti-HIV-1 immune responses. These findings strongly support the advisability of using CpG ODN as a Th1 inducing adjuvant when immunizing human populations with a strong pre-existent Th2 immune profile. (C) 2002 Published by Elsevier Science Ltd.
引用
收藏
页码:2684 / 2692
页数:9
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