HIV-1 gp120 and immune network

被引:2
|
作者
Metlas, R
Veljkovic, V
机构
[1] Inst Nucl Sci VINCA, Ctr Multidisciplinary Res, YU-11001 Belgrade, Serbia
[2] Diapharm Ltd, Guernsey, Channel Islands, England
关键词
HIV-1; gp120; V3; loop; immunoglobulin; immune network;
D O I
10.1080/08830180490432758
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has been demonstrated that the immunodominant V3 loop of HIV-1 gp120 and its flanking regions bear sequence and structural homology to the framework and complementarity-determining regions of human immunoglobulins. It has been proposed that the Ig-like domain of gp120 might encode idiotypes and in this way permit HIV-1 entry into the immune regulatory network. This notion is strongly supported by results demonstrating that the anti-V3 loop and anti-Ig antibodies of healthy individuals share complementary structure and that V3 reactive antibodies are present in HIV-negative sera. This might be the mechanism by which HIV induces immunological abnormalities, and it should be taken into consideration in AIDS vaccine development.
引用
收藏
页码:413 / 422
页数:10
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