Modi William S, Goedert James J, Strathdee Steffanie, Buchbinder Susan, Detels Roger, Donfield Sharyne, O'Brien Stephen J, Winkler Cheryl
SAIC Frederick and the Laboratory of Genomic Diversity, National Cancer Institute, Frederick, Maryland, USA.
AIDS. 2003 Nov 7;17(16):2357-65. doi: 10.1097/00002030-200311070-00011.
MCP-1 (CCL2), MCP-3 (CCL7), and eotaxin (CCL11) are genes for CC chemokines clustered on the long arm of chromosome 17. Previous studies have implicated these chemokines in monocyte recruitment, viral replication, and anti-HIV cytotoxic T cell responses. An epidemiological analysis identified genetic variants influencing HIV-1 transmission and disease progression.
Genomic DNA from over 3000 participants enrolled in five natural history cohorts in the United States were analyzed. Nine single nucleotide polymorphisms (SNP) covering 33 kb containing these three genes were genotyped using the polymerase chain reaction. Distortions in allele, genotype, and haplotype frequencies were assessed with respect to HIV-1 transmission and rates of disease progression using categorical and survival analyses.
Extensive linkage disequilibrium was observed. Three SNP (-2136T located in the MCP-1 promoter region, 767G in intron 1 of MCP-1, and -1385A in the Eotaxin promoter) were nearly always found together on a 31 kb haplotype (H7) containing the three genes. Frequencies of the three variants and the H7 haplotype were significantly elevated (odds ratio, 0.6; P = 0.005-0.01) in uninfected European-Americans repeatedly exposed to HIV-1 through high-risk sexual behavior or contaminated blood products.
Although the extensive linkage disequilibrium precludes positive identification of the causal variant, the results suggest that genetic variation in the H7 region influences susceptibility to HIV-1 infection. Since these chemokines do not bind the primary HIV-1 coreceptors CCR5 or CXCR4, the observed influence on transmission may result from activation of the immune system in response to infection rather than receptor blockage.
单核细胞趋化蛋白-1(MCP-1,即CCL2)、单核细胞趋化蛋白-3(MCP-3,即CCL7)和嗜酸性粒细胞趋化因子(eotaxin,即CCL11)是CC趋化因子的基因,它们聚集在17号染色体的长臂上。先前的研究表明这些趋化因子与单核细胞募集、病毒复制以及抗HIV细胞毒性T细胞反应有关。一项流行病学分析确定了影响HIV-1传播和疾病进展的基因变异。
对参与美国五个自然史队列研究的3000多名参与者的基因组DNA进行了分析。使用聚合酶链反应对覆盖这三个基因的33 kb区域内的九个单核苷酸多态性(SNP)进行基因分型。通过分类分析和生存分析评估等位基因、基因型和单倍型频率在HIV-1传播和疾病进展率方面的偏差。
观察到广泛的连锁不平衡。三个SNP(位于MCP-1启动子区域的-2136T、MCP-1内含子1中的767G以及嗜酸性粒细胞趋化因子启动子中的-1385A)几乎总是一起出现在一个包含这三个基因的31 kb单倍型(H7)上。在通过高危性行为或受污染血液制品反复接触HIV-1的未感染欧洲裔美国人中,这三个变异和H7单倍型的频率显著升高(优势比为0.6;P = 0.005 - 0.01)。
尽管广泛的连锁不平衡妨碍了对因果变异的明确识别,但结果表明H7区域的基因变异会影响对HIV-1感染的易感性。由于这些趋化因子不与主要的HIV-1共受体CCR5或CXCR4结合,观察到的对传播的影响可能是由于免疫系统对感染的反应激活,而非受体阻断。