Roederer Mario, Quaye Lydia, Mangino Massimo, Beddall Margaret H, Mahnke Yolanda, Chattopadhyay Pratip, Tosi Isabella, Napolitano Luca, Terranova Barberio Manuela, Menni Cristina, Villanova Federica, Di Meglio Paola, Spector Tim D, Nestle Frank O
ImmunoTechnology Section, Vaccine Research Center, NIAID, NIH, Bethesda, MD 20892, USA.
Department of Twin Research & Genetic Epidemiology, King's College London, London SE1 7EH, UK.
Cell. 2015 Apr 9;161(2):387-403. doi: 10.1016/j.cell.2015.02.046. Epub 2015 Mar 12.
Despite recent discoveries of genetic variants associated with autoimmunity and infection, genetic control of the human immune system during homeostasis is poorly understood. We undertook a comprehensive immunophenotyping approach, analyzing 78,000 immune traits in 669 female twins. From the top 151 heritable traits (up to 96% heritable), we used replicated GWAS to obtain 297 SNP associations at 11 genetic loci, explaining up to 36% of the variation of 19 traits. We found multiple associations with canonical traits of all major immune cell subsets and uncovered insights into genetic control for regulatory T cells. This data set also revealed traits associated with loci known to confer autoimmune susceptibility, providing mechanistic hypotheses linking immune traits with the etiology of disease. Our data establish a bioresource that links genetic control elements associated with normal immune traits to common autoimmune and infectious diseases, providing a shortcut to identifying potential mechanisms of immune-related diseases.
尽管最近发现了与自身免疫和感染相关的基因变异,但对稳态期间人类免疫系统的基因控制仍知之甚少。我们采用了一种全面的免疫表型分析方法,分析了669对女性双胞胎的78000个免疫特征。从排名前151的可遗传特征(遗传率高达96%)中,我们使用重复的全基因组关联研究(GWAS)在11个基因位点获得了297个单核苷酸多态性(SNP)关联,解释了19个特征中高达36%的变异。我们发现了与所有主要免疫细胞亚群的典型特征的多种关联,并揭示了调节性T细胞基因控制的见解。该数据集还揭示了与已知赋予自身免疫易感性的基因位点相关的特征,提供了将免疫特征与疾病病因联系起来的机制假说。我们的数据建立了一个生物资源,将与正常免疫特征相关的基因控制元件与常见的自身免疫和感染性疾病联系起来,为识别免疫相关疾病的潜在机制提供了一条捷径。