Kumar Amrendra, Das Sudipta, Agrawal Anurag, Mukhopadhyay Indranil, Ghosh Balaram
Molecular Immunogenetics Laboratory, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
Centre of Excellence for Translational Research in Asthma and Lung Disease, CSIR-Institute of Genomics and Integrative Biology, Delhi, India.
J Hum Genet. 2015 Aug;60(8):443-8. doi: 10.1038/jhg.2015.45. Epub 2015 May 21.
Asthma is a complex, multifactorial disease resulting due to dysregulated immune responses. Genetic factors contribute significantly to asthma pathogenesis, and identification of these factors is one of the major goals in understanding the disease. Th1/Th2 helper differentiation has a critical role in modulating the phenotypes associated with atopic asthma. This study was aimed at identifying genetic modifiers of asthma in selected genes involved in T helper differentiation. A total of 354 single-nucleotide polymorphisms (SNPs) in 33 candidate genes were genotyped in a case-control cohort (cases=147, controls=199) and families (n=247) using Illumina's Golden Gate Assay. Five SNPs, rs3733475A/C (IRF2), rs2069832A/G (IL6), rs2012075G/A (IFNGR2) and rs1400656G/A (STAT4) and rs1805011C/A (IL4RA) were found to be associated with asthma in family based as well as in case-control analyses (P=0.002, P=0.001, P=0.004, P=0.003 and P=0.001, respectively). Interestingly, the minor alleles at these loci showed a protective effect. A five loci haplotype, TAACG, in IRF2 gene, was significantly associated with asthma in families (P=1.1 × 10(-6)) and in case-control cohort (P=0.01). In conclusion, our studies led to identification of some key candidate genes, namely IRF2, IL6, IFNGR2, STAT4 and IL4RA that modulate genetic susceptibility to asthma in the Indian population. Also, this is the first report of independent association of IL6 gene polymorphism with atopic asthma.
哮喘是一种由于免疫反应失调导致的复杂多因素疾病。遗传因素在哮喘发病机制中起着重要作用,识别这些因素是理解该疾病的主要目标之一。Th1/Th2辅助性T细胞分化在调节与特应性哮喘相关的表型方面起着关键作用。本研究旨在识别参与T辅助性细胞分化的选定基因中哮喘的遗传修饰因子。使用Illumina的Golden Gate检测法,对一个病例对照队列(病例 = 147,对照 = 199)和家庭(n = 247)中的33个候选基因中的总共354个单核苷酸多态性(SNP)进行基因分型。发现五个SNP,即rs3733475A/C(IRF2)、rs2069832A/G(IL6)、rs2012075G/A(IFNGR2)、rs1400656G/A(STAT4)和rs1805011C/A(IL4RA)在基于家庭以及病例对照分析中与哮喘相关(P分别为0.002、0.001、0.004、0.003和0.001)。有趣的是,这些位点的次要等位基因显示出保护作用。IRF2基因中的一个五个位点的单倍型TAACG在家庭中(P = 1.1×10⁻⁶)和病例对照队列中(P = 0.01)与哮喘显著相关。总之,我们的研究导致识别出一些关键候选基因,即IRF2、IL6、IFNGR2、STAT4和IL4RA,它们调节印度人群对哮喘的遗传易感性。此外,这是IL6基因多态性与特应性哮喘独立关联的首次报告。