Antigen-driven C-C chemokine-mediated HIV-1 suppression by CD4(+) T cells from exposed uninfected individuals expressing the wild-type CCR-5 allele

被引:113
作者
Furci, L
Scarlatti, G
Burastero, S
Tambussi, G
Colognesi, C
Quillent, C
Longhi, R
Loverro, P
Borgonovo, B
Gaffi, D
Carrow, E
Malnati, M
Lusso, P
Siccardi, AG
Lazzarin, A
Beretta, A
机构
[1] SIDA,CTR INTEGRE RECH BIOCLIN,CIRBS,F-75014 PARIS,FRANCE
[2] SAN RAFFAELE SCI INST,DEPT BIOL & TECHNOL RES,I-20132 MILAN,ITALY
关键词
D O I
10.1084/jem.186.3.455
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite repeated exposure to HIV-1, certain individuals remain persistently uninfected. Such exposed uninfected (EU) people show evidence of HIV-1-specific T cell immunity and, in rare cases, selective resistance to infection by macrophage-tropic strains of HIV-1. The latter has been associated with a 32-base pair deletion in the C-C chemokine receptor gene CCR-5, the major coreceptor of macrophage-tropic strains of HIV-1. We have undertaken an analysis of the HIV-specific T cell responses in 12 EU individuals who were either homozygous for the wild-type CCR-5 allele or heterozygous for the deletion allele (CCR-5 Delta 32). We have found evidence of an oligoclonal T cell response mediated by helper T cells specific for a conserved region of the HIV-1 envelope. These cells produce very high levels of C-C chemokines when stimulated by the specific antigen and suppress selectively the replication of macrophage-tropic, but not T cell-tropic, strains of HIV-1. These chemokine-producing helper cells may be part of a protective immune response that could be potentially exploited for vaccine development.
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页码:455 / 460
页数:6
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