Beghé B, Barton S, Rorke S, Peng Q, Sayers I, Gaunt T, Keith T P, Clough J B, Holgate S T, Holloway J W
Divisions of Human Genetics Infection, Inflammation and Repair, School of Medicine, University of Southampton, UK.
Clin Exp Allergy. 2003 Aug;33(8):1111-7. doi: 10.1046/j.1365-2222.2003.01731.x.
IL-4 by binding to its receptor (IL-4R) is essential for the development of airway inflammation present in asthma, through the induction of IgE synthesis in B cells and differentiation of T cells to a Th2 phenotype.
To investigate the role of four common polymorphisms in the IL-4 (IL4-34CT and IL4-589CT) and IL-4Ralpha chain (IL4RAI50V and IL4RAQ576R) genes in conferring susceptibility to the development of atopy and/or asthma.
Two polymorphisms in the IL-4 gene promoter, IL4-34CT and IL4-589CT, and two polymorphisms in the IL-4Ralpha chain gene, IL4RAI50V and IL4RAQ576R, have been genotyped using PCR-based methods in 341 asthmatic families and in 184 non-asthmatic adults recruited from the south of England.
Case-control analysis did not reveal differences in the distribution of the four polymorphisms between asthmatics and controls. However, the transmission disequilibrium test showed that the IL4-589 T allele was preferentially transmitted to asthmatic children (P=0.036) and that the IL4RAQ576 was preferentially transmitted to children with atopic asthma (P=0.018). Haplotype analysis showed a strong association between the IL4-34T/-589T haplotype and asthma per se (P=0.041), and a strong association between the IL4RA I50/Q576 haplotype and atopic asthma (P=0.006).
Our data suggest that polymorphisms in the IL-4 and IL-4Ralpha chain genes might play a role both conferring susceptibility to and modulating severity of atopy and asthma.
白细胞介素-4(IL-4)通过与其受体(IL-4R)结合,在哮喘气道炎症的发展过程中起着至关重要的作用,它可诱导B细胞合成IgE,并使T细胞分化为Th2表型。
研究白细胞介素-4(IL-4)基因(IL4-34CT和IL4-589CT)和白细胞介素-4受体α链基因(IL4RAI50V和IL4RAQ576R)中的四种常见多态性在特应性和/或哮喘发病易感性中的作用。
采用基于聚合酶链反应(PCR)的方法,对来自英格兰南部的341个哮喘家族和184名非哮喘成年人进行基因分型,检测IL-4基因启动子中的两种多态性(IL4-34CT和IL4-589CT)以及IL-4受体α链基因中的两种多态性(IL4RAI50V和IL4RAQ576R)。
病例对照分析未发现哮喘患者与对照者之间这四种多态性分布存在差异。然而,传递不平衡检验显示,IL4-589 T等位基因优先传递给哮喘儿童(P = 0.036),IL4RAQ576优先传递给特应性哮喘儿童(P = 0.018)。单倍型分析显示,IL4-34T/-589T单倍型与哮喘本身之间存在强关联(P = 0.041),IL4RA I50/Q576单倍型与特应性哮喘之间存在强关联(P = 0.006)。
我们的数据表明,IL-4和IL-4受体α链基因中的多态性可能在赋予特应性和哮喘易感性以及调节其严重程度方面发挥作用。