Do Hervé, Vasilescu Alexandre, Diop Gora, Hirtzig Thomas, Coulonges Cédric, Labib Taoufik, Heath Simon C, Spadoni Jean-Louis, Therwath Amu, Lathrop Mark, Matsuda Fumihiko, Zagury Jean-François
Equipe génomique, bioinformatique et pathologies du système immunitaire, INSERM U736, 15 rue de l'Ecole de Médecine, 75006, Paris, France.
Immunogenetics. 2006 Apr;58(2-3):89-98. doi: 10.1007/s00251-005-0072-3. Epub 2006 Feb 21.
We have performed an extensive analysis of Th1/Th2 cytokine receptors IL2Ralpha, IL4Ralpha, IL10Ralpha, and IFNgammaR1 gene polymorphisms to evaluate their impact on AIDS progression. The coding regions and promoters of these genes were sequenced in the genetics of resistance to immunodeficiency virus cohort, composed of 327 HIV-1-positive patients with extreme progression phenotypes, slow and rapid progressors, and of 446 healthy control subjects, all of them of Caucasian descent. Overall, 104 single nucleotide polymorphisms and four insertions/deletions with a minor allelic frequency higher than 1% were identified, 21 of them being newly characterized. We observed weak associations for 13 polymorphisms of IL2Ralpha, IL4Ralpha, IL10Ralpha, and IFNgammaR1, and 11 haplotypes of IL2Ralpha, IL4Ralpha, and IFNgammaR1. However, we could not relate these positive signals to any relevant biological information on the gene function. To affirm these putative associations in AIDS, further confirmation on other AIDS cohorts will be needed. This complete catalog of polymorphisms in IL2Ralpha, IL4Ralpha, IL10Ralpha, and IFNgammaR1 cytokine receptor genes should also be useful for investigating associations in other immune-related diseases.
我们对Th1/Th2细胞因子受体IL2Rα、IL4Rα、IL10Rα和IFNγR1基因多态性进行了广泛分析,以评估它们对艾滋病进展的影响。在免疫缺陷病毒抗性遗传学队列中对这些基因的编码区和启动子进行了测序,该队列由327名具有极端进展表型的HIV-1阳性患者(进展缓慢者和快速进展者)以及446名健康对照受试者组成,他们均为白种人后裔。总体而言,共鉴定出104个单核苷酸多态性和4个插入/缺失,其次要等位基因频率高于1%,其中21个为新鉴定的。我们观察到IL2Rα、IL4Rα、IL10Rα和IFNγR1的13个多态性以及IL2Rα、IL4Rα和IFNγR1的11个单倍型存在弱关联。然而,我们无法将这些阳性信号与基因功能的任何相关生物学信息联系起来。为了证实这些在艾滋病中的假定关联,需要在其他艾滋病队列中进一步确认。IL2Rα、IL4Rα、IL10Rα和IFNγR1细胞因子受体基因的这个完整多态性目录对于研究其他免疫相关疾病中的关联也应该是有用的。