Nuolivirta Kirsi, Törmänen Sari, Teräsjärvi Johanna, Vuononvirta Juho, Koponen Petri, Korppi Matti, Helminen Merja, Peltola Ville, He Qiushui
Department of Pediatrics, Seinäjoki Central Hospital, Seinäjoki, Finland.
Center for Child Health Research, Tampere University and University Hospital, Tampere, Finland.
Sci Rep. 2016 Aug 8;6:31165. doi: 10.1038/srep31165.
Innate immunity receptors play a critical role in host defence, as well as in allergy and asthma. The aim of this exploratory study was to evaluate whether there are associations between TLR7 rs179008, TLR8 rs2407992, TLR9 rs187084 or TLR10 rs4129009 polymorphisms and viral findings, clinical characteristics or subsequent wheezing in infants with bronchiolitis. In all, 135 full-term infants were hospitalized for bronchiolitis at age less than 6 months: 129 of them were followed-up until the age of 1.5 years. The outcome measures were repeated wheezing, use of inhaled corticosteroids, atopic dermatitis during the first 1.5 years of life and total serum immunoglobulin E (IgE). There were no significant associations between the genotypes or allele frequencies of TLR7 rs179008, TLR8 rs2407992, TLR9 rs187084 or TLR10 rs4129009 polymorphisms and clinical characteristics or the severity of bronchiolitis during hospitalization. During follow-up, repeated wheezing was more common in children with TLR9 rs187084 variant genotype CC (30.5%) than in children with TLR9 wild-type genotype TT (12.2%) (p = 0.02, aOR 2.73, 95% CI 1.02-7.29). The TLR10 rs4129009 minor allele G was associated with elevated total serum IgE. TLR9 rs187084 gene polymorphism may be associated with post-bronchiolitis wheezing, and TLR10 rs4129009 gene polymorphism may be associated with atopy.
天然免疫受体在宿主防御以及过敏和哮喘中发挥着关键作用。本探索性研究的目的是评估Toll样受体7(TLR7)rs179008、Toll样受体8(TLR8)rs2407992、Toll样受体9(TLR9)rs187084或Toll样受体10(TLR10)rs4129009基因多态性与毛细支气管炎婴儿的病毒学检查结果、临床特征或随后的喘息之间是否存在关联。共有135名足月婴儿在6个月龄前因毛细支气管炎住院:其中129名婴儿随访至1.5岁。观察指标为反复喘息、吸入性糖皮质激素的使用、生命最初1.5年内的特应性皮炎以及血清总免疫球蛋白E(IgE)。TLR7 rs179008、TLR8 rs2407992、TLR9 rs187084或TLR10 rs4129009基因多态性的基因型或等位基因频率与住院期间毛细支气管炎的临床特征或严重程度之间无显著关联。在随访期间,TLR9 rs187084变异基因型CC的儿童反复喘息更为常见(30.5%),高于TLR9野生型基因型TT的儿童(12.2%)(p = 0.02,调整后比值比2.73,95%可信区间1.02 - 7.29)。TLR10 rs4129009次要等位基因G与血清总IgE升高有关。TLR9 rs187084基因多态性可能与毛细支气管炎后喘息有关,而TLR10 rs4129009基因多态性可能与特应性有关。