Nuolivirta Kirsi, Vuononvirta Juho, Peltola Ville, Koponen Petri, Helminen Merja, He Qiushui, Korppi Matti
Seinäjoki Central Hospital, Seinäjoki, Finland.
Acta Paediatr. 2013 Dec;102(12):1160-4. doi: 10.1111/apa.12425.
Expression of toll-like receptor (TLR) 2 subfamily genes, including genes encoding TLR1, TLR2, TLR6 and TLR10, have been connected to allergy and asthma. This controlled study investigated the association of TLR1, TLR2 and TLR6 gene polymorphisms with clinical characteristics and subsequent wheezing in young infants with bronchiolitis.
In all, 129 full-term infants hospitalised for bronchiolitis at the age of <6 months were clinically followed up until a mean age of 18 months. Genotyping of the TLR1 T1805G, TLR2 G2258A and TLR6 C745T polymorphisms was carried out by pyrosequencing and in 318 healthy, Finnish controls.
There were no significant associations between TLR1, TLR2 or TLR6 genotypes and severity of bronchiolitis or risk of postbronchiolitis wheezing. TLR6 polymorphism was associated with allergy in univariate analyses. Minor allele frequency (MAF) in the TLR1 gene (17%) in the hospitalised children was similar to our Finnish controls, but different to European controls from other studies. MAF in the TLR6 gene was 50% versus 41% in both the Finnish and European controls. MAF in the TLR2 gene was low (3%) in study subjects and in both controls.
TLR2 subfamily gene polymorphisms were not associated with severity of bronchiolitis or risk of postbronchiolitis wheezing.
Toll样受体(TLR)2亚家族基因的表达,包括编码TLR1、TLR2、TLR6和TLR10的基因,已被证实与过敏和哮喘有关。这项对照研究调查了TLR1、TLR2和TLR6基因多态性与小儿毛细支气管炎临床特征及随后喘息发作之间的关联。
共有129名6个月以下因毛细支气管炎住院的足月儿接受临床随访,直至平均年龄达到18个月。采用焦磷酸测序法对TLR1 T1805G、TLR2 G2258A和TLR6 C745T基因多态性进行基因分型,并与318名健康的芬兰对照者进行比较。
TLR1、TLR2或TLR6基因分型与毛细支气管炎的严重程度或毛细支气管炎后喘息发作的风险之间无显著关联。在单因素分析中,TLR6基因多态性与过敏有关。住院儿童中TLR1基因的次要等位基因频率(MAF)(17%)与我们的芬兰对照者相似,但与其他研究中的欧洲对照者不同。芬兰和欧洲对照者中TLR6基因的MAF分别为50%和41%。研究对象和两组对照者中TLR2基因的MAF均较低(3%)。
TLR2亚家族基因多态性与毛细支气管炎的严重程度或毛细支气管炎后喘息发作的风险无关。