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IL-13 rs20541、FOXP3 rs3761548 基因多态性与血清 IL-13 水平与埃及过敏性哮喘患者的关联。

Association of IL-13 rs20541, FOXP3 rs3761548 genes polymorphisms and serum level of IL-13 with allergic asthma in Egyptian patients.

机构信息

Department of Microbiology and Immunology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.

Department of Chest, Faculty of Medicine, Zagazig University, Zagazig, Egypt.

出版信息

Egypt J Immunol. 2024 Jul;31(3):15-27.

Abstract

The interleukin 13 (IL-13) gene single nucleotide polymorphisms (SNPs) are frequently linked to increased vulnerability to allergic asthma. Forkhead box protein P3 (FOXP3) is an important molecule in the formation of regulatory T cells (Treg). The genetic variants that alter FOXP3 function may have a role in the development of asthma and other allergic disorders. We aimed to determine the association of IL-13 rs20541, FOXP3 rs3761548 genes SNPs and serum levels of IL-13 with allergic asthma patients. In this case-control study, 41 Egyptian patients with allergic asthma were included. Age and gender matched. 41 normal volunteers were considered the controls. All subjects were examined for IL-13 rs20541 and FOXP3 rs3761548 SNPs by the polymerase chain reaction /restriction fragment length polymorphism technique. The serum level of IL-13 was assessed by the enzyme linked immunosorbent assay (ELISA). AA genotype at IL-13 rs20541 SNP was statistically significantly different between the studied groups (p= 0.042). Also, a statistically significant difference was detected when compared AA genotype to GG genotype as AA genotype was three times at risk for asthma (p1=0.031) (OR=3.95) and A allele increased the risk of asthma by about 3 times (OR=3.2). AA genotype at FOXP3 rs3761548 SNP was statistically significantly different between the studied groups (p=0.013). Also, a statistically significant difference was detected when compared AA genotype to CC genotype as AA genotype was 7 times at risk for asthma (p1=0.003) (OR=7.04) and A allele increased the risk of asthma by about 3 times (p<0.001) (OR=3.07). The serum level of IL-13 was statistically significant different between both groups (p<0.001). We can conclude that IL-13 could be a useful tool for predicting allergic asthma. Patients with AA genotype of IL-13 rs20541 and AA genotype of FOXP3 rs3761548 have a higher risk for developing allergic asthma.

摘要

白细胞介素 13(IL-13)基因单核苷酸多态性(SNP)与过敏性哮喘的易感性增加密切相关。叉头框蛋白 P3(FOXP3)是调节性 T 细胞(Treg)形成的重要分子。改变 FOXP3 功能的遗传变异可能在哮喘和其他过敏性疾病的发展中起作用。我们旨在确定 IL-13 rs20541、FOXP3 rs3761548 基因 SNPs 与过敏性哮喘患者的关系以及血清中 IL-13 的水平。在这项病例对照研究中,纳入了 41 例埃及过敏性哮喘患者。年龄和性别匹配。41 名正常志愿者被认为是对照组。所有受试者均通过聚合酶链反应/限制性片段长度多态性技术检测 IL-13 rs20541 和 FOXP3 rs3761548 SNP。通过酶联免疫吸附试验(ELISA)评估血清中 IL-13 的水平。IL-13 rs20541 SNP 的 AA 基因型在研究组之间存在统计学差异(p=0.042)。当比较 AA 基因型与 GG 基因型时,也发现了统计学差异,因为 AA 基因型患哮喘的风险增加了三倍(p1=0.031)(OR=3.95),A 等位基因使哮喘的风险增加了约三倍(OR=3.2)。FOXP3 rs3761548 SNP 的 AA 基因型在研究组之间存在统计学差异(p=0.013)。当比较 AA 基因型与 CC 基因型时,也发现了统计学差异,因为 AA 基因型患哮喘的风险增加了 7 倍(p1=0.003)(OR=7.04),A 等位基因使哮喘的风险增加了约 3 倍(p<0.001)(OR=3.07)。两组之间的血清 IL-13 水平存在统计学差异(p<0.001)。我们可以得出结论,IL-13 可能是预测过敏性哮喘的有用工具。IL-13 rs20541 的 AA 基因型和 FOXP3 rs3761548 的 AA 基因型的患者发生过敏性哮喘的风险更高。

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