白细胞介素13 (IL13)基因多态性Arg130Gln对血清总免疫球蛋白(IgE)水平和干扰素γ基因表达的影响

B. Smolková, J. Tulinská, L. P. Murinova, Verona Buocikova, A. Líšková, K. Rausova, M. Kuricová, H. Patayová, Maria Sustrova, E. N. Svorcova, Silvia Ilavská, M. Szabová, Tomáš Nemessányi, Eva Jahnova, Maria Dusinska, P. Ciznar, Laurence J. Fuortes
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引用次数: 11

摘要

本横断面研究旨在通过靶向导致儿童早期特应性疾病的白细胞介素(IL)−4/IL‐13信号通路的变异来研究遗传易感性的程度。我们评估了五种单核苷酸多态性IL4 C‐590T、IL13 C‐1055T、IL13 Arg130Gln、IL4RA Ile50Val和IL4RA Gln576Arg在控制血清总免疫球蛋白(Ig)E水平中的作用。此外,我们分析了它们与五种在炎症和抗炎免疫反应中起关键作用的细胞因子(IL‐4、IL‐13、干扰素(IFN)‐γ、IL‐8和IL‐10)基因表达变化的关系。测定了386例1-8岁儿童血清中总IgE和抗原特异性IgE水平以及外周血中选定细胞因子的基因表达。采用TaqMan等位基因鉴别、扩增难解突变系统-聚合酶链反应(ARMS-PCR)和限制性片段长度多态性(RFLP)方法进行基因分型。总IgE和抗原特异性IgE水平在正常范围内的儿童的所有基因型均处于Hardy-Weinberg平衡。基因表达分析采用TaqMan基因表达法。我们发现IL13 Arg130Gln变异等位基因携带者的总IgE水平升高[优势比(OR) = 1.84;95%置信区间(CI) = 1.16‐2.93]。这种效应在男孩中更为明显(OR = 2.31;95% ci = 1.25‐4.28)。然而,在其他四种变异中没有观察到显著的关联。我们发现携带Arg130等位基因的血清总IgE水平升高的儿童中IFN‐γ上调(P = 0.005)。IL4、IL8、IL10基因表达无差异,IL13基因表达低于检测限。IL13 Arg130Gln基因型可能通过调节血清总IgE水平和影响IFN‐γ基因表达而在过敏遗传易感性中发挥作用。
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Impact of interleukin 13 (IL13) genetic polymorphism Arg130Gln on total serum immunoglobulin (IgE) levels and interferon (IFN)‐γ gene expression
This cross‐sectional study was designed to investigate the extent of genetic susceptibility by targeting variants in interleukin (IL)−4/IL‐13 signalling pathways leading to atopic disease in early childhood. We evaluated involvement of five single nucleotide polymorphisms IL4 C‐590T, IL13 C‐1055T, IL13 Arg130Gln, IL4RA Ile50Val and IL4RA Gln576Arg, in the control of serum total and antigen‐specific immunoglobulin (Ig)E levels. Furthermore, we analysed their association with changes in gene expression of five cytokines having key roles in inflammatory and anti‐inflammatory immune response [IL‐4, IL‐13, interferon (IFN)‐γ, IL‐8 and IL‐10]. Total and antigen‐specific IgE levels in serum and gene expression of selected cytokines in peripheral blood were measured in 386 children aged 1–8 years. TaqMan allelic discrimination, amplification refractory mutation system–polymerase chain reaction (ARMS–PCR) and restriction fragment length polymorphisms (RFLP) methods validated by sequencing were used for genotyping. All genotypes for children with total and antigen‐specific IgE levels in the normal range were in Hardy–Weinberg equilibrium. Gene expression analyses were carried out using TaqMan gene expression assays. We found elevated total IgE levels in carriers of IL13 Arg130Gln variant allele [odds ratio (OR) = 1·84; 95% confidence interval (CI) = 1·16‐2·93]. This effect was more apparent for boys (OR = 2·31; 95% CI = 1·25‐4·28). However, no significant association was observed for the other four variants examined. We found up‐regulation of IFN‐γ in children with elevated serum total IgE levels carrying the Arg130 allele (P = 0·005). No differences were found for IL4, IL8 or IL10, while IL13 gene expression was under the detection limit. IL13 Arg130Gln genotypes can play a role in genetic susceptibility to allergy via regulation of serum total IgE levels and affecting IFN‐γ gene expression.
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