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一项艾滋病非进展队列的全基因组关联研究强调了HLA基因所起的作用(ANRS全基因组关联研究02)。

Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).

作者信息

Limou Sophie, Le Clerc Sigrid, Coulonges Cédric, Carpentier Wassila, Dina Christian, Delaneau Olivier, Labib Taoufik, Taing Lieng, Sladek Rob, Deveau Christiane, Ratsimandresy Rojo, Montes Matthieu, Spadoni Jean-Louis, Lelièvre Jean-Daniel, Lévy Yves, Therwath Amu, Schächter François, Matsuda Fumihiko, Gut Ivo, Froguel Philippe, Delfraissy Jean-François, Hercberg Serge, Zagury Jean-François

机构信息

Conservatoire National des Arts et Métiers, Université Paris 7, Paris, France.

出版信息

J Infect Dis. 2009 Feb 1;199(3):419-26. doi: 10.1086/596067.

Abstract

To elucidate the genetic factors predisposing to AIDS progression, we analyzed a unique cohort of 275 human immunodeficiency virus (HIV) type 1-seropositive nonprogressor patients in relation to a control group of 1352 seronegative individuals in a genomewide association study (GWAS). The strongest association was obtained for HCP5 rs2395029 (P=6.79x10(-10); odds ratio, 3.47) and was possibly linked to an effect of sex. Interestingly, this single-nucleotide polymorphism (SNP) was in high linkage disequilibrium with HLA-B, MICB, TNF, and several other HLA locus SNPs and haplotypes. A meta-analysis of our genomic data combined with data from the previously conducted Euro-CHAVI (Center for HIV/AIDS Vaccine Immunology) GWAS confirmed the HCP5 signal (P=3.02x10(-19)) and identified several new associations, all of them involving HLA genes: MICB, TNF, RDBP, BAT1-5, PSORS1C1, and HLA-C. Finally, stratification by HCP5 rs2395029 genotypes emphasized an independent role for ZNRD1, also in the HLA locus, and this finding was confirmed by experimental data. The present study, the first GWAS of HIV-1 nonprogressors, underscores the potential for some HLA genes to control disease progression soon after infection.

摘要

为了阐明导致艾滋病进展的遗传因素,我们在一项全基因组关联研究(GWAS)中,分析了一组独特的275名1型人类免疫缺陷病毒(HIV)血清反应阳性的疾病非进展者患者,并与1352名血清反应阴性个体的对照组进行了比较。HCP5基因的rs2395029位点显示出最强的关联性(P = 6.79×10⁻¹⁰;优势比为3.47),并且可能与性别效应有关。有趣的是,这个单核苷酸多态性(SNP)与HLA - B、MICB、TNF以及其他几个HLA基因座的SNP和单倍型处于高度连锁不平衡状态。对我们的基因组数据与先前进行的欧洲HIV/AIDS疫苗免疫学中心(Euro - CHAVI)GWAS数据进行的荟萃分析证实了HCP5基因的信号(P = 3.02×10⁻¹⁹),并确定了几个新的关联,所有这些关联都涉及HLA基因:MICB、TNF、RDBP、BAT1 - 5、PSORS1C1和HLA - C。最后,按HCP5 rs2395029基因型进行分层分析,强调了同样位于HLA基因座的ZNRD1的独立作用,这一发现得到了实验数据的证实。本研究作为首次对HIV - 1疾病非进展者进行的GWAS,强调了某些HLA基因在感染后不久控制疾病进展的潜力。

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