The role of a mutant CCR5 allele in HIV-1 transmission and disease progression

被引:1070
|
作者
Huang, YX
Paxton, WA
Wolinsky, SM
Neumann, AU
Zhang, LQ
He, T
Kang, S
Ceradini, D
Jin, ZQ
Yazdanbakhsh, K
Kunstman, K
Erickson, D
Dragon, E
Landau, NR
Phair, J
Ho, DD
Koup, RA
机构
[1] AARON DIAMOND AIDS RES CTR,NEW YORK,NY 10016
[2] ROCKEFELLER UNIV,NEW YORK,NY 10016
[3] NORTHWESTERN UNIV,SCH MED,DEPT MED,CHICAGO,IL 60611
[4] LOS ALAMOS NATL LAB,DIV THEORET,LOS ALAMOS,NM 87545
[5] NEW YORK BLOOD CTR,LINDSLEY F KIMBALL RES INST,LAB IMMUNOCHEM,NEW YORK,NY 10021
[6] ROCHE MOL SYST,BRANCHBURG,NJ 08876
关键词
D O I
10.1038/nm1196-1240
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A 32-nucleotide deletion (Delta 32) within the beta-chemokine receptor 5 (CCR5) gene has been described in subjects who remain uninfected despite extensive exposure to HIV-1. This allele was found to be common in the Caucasian population with a frequency of 0.0808, but was not found in people of African or Asian ancestry. To determine its role in HIV-1 transmission and disease progression, we analyzed the CCR5 genotype of 1252 homosexual men enrolled in the Chicago component of the Multicenter AIDS Cohort Study (MACS). No infected participant was found to be homozygous for the Delta 32 allele, whereas 3.6% of at-risk but uninfected Caucasian participants were homozygous, showing the highly protective role of this genotype against sexual acquisition of HIV-1. No evidence was found to suggest that heterozygotes were protected against HIV-1 infection, but a limited protective role against disease progression was noted. The Delta 32 allele of CCR5 is therefore an important host factor in HIV-1 transmission and pathogenesis.
引用
收藏
页码:1240 / 1243
页数:4
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