Biology Department, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Skin Research Centre, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Immunol Invest. 2022 Feb;51(2):343-356. doi: 10.1080/08820139.2020.1832113. Epub 2020 Oct 13.
T-helper 2 (Th2)-associated cytokines are involved in the pathogenesis of bullous pemphigoid (BP), an autoimmune skin disease. Increased expression of Th2 cytokines such as interleukin-4 (IL-4), IL-5, IL-6, IL-10, and IL-13 have been observed in serum, skin biopsies and/or blister fluid. This study aimed to uncover a possible association between Th2 cytokine genetic variations and susceptibility to BP.
In a cohort study, blood samples of BP patients and controls were obtained and variations in IL-4 (rs2243250 and rs2070874), IL-4R (rs1805010), IL-5 (rs2069812), IL-6 (rs1800795), IL-10 (rs1800896, rs1800871, and rs1800872), and IL-13 (rs1800925 and rs20541) were genotyped by PCR-RFLP assays. Furthermore, quantitative expression levels of IL-13 gene were evaluated by real-time RT-PCR analysis.
Among the studied variations, a significantly higher frequency of the C-allele was observed in IL-13 gene variation (rs1800925) in the healthy individuals than BP patients. This may indicate a protective effect of C-allele on predisposition to BP. Considering individuals carrying polymorphic genotypes compared to wild genotype, the minor G-allele of IL-4R rs1805010 and A-allele of IL-13 rs20541 had a promotive and protective effect, respectively, on predisposing to the development of BP. No significant difference in IL-13 mRNA expression was detected between BP patients and healthy individuals.
Our results indicate that IL-13 rs1800925 variation may be a protective genetic marker for the development of BP. Given this preventive effect against BP, therapeutic strategies could potentially be developed interfering with the functions of IL-13 cytokine, which seems to be integral in the pathogenesis of eosinophilic inflammatory disorders, such as BP.
辅助性 T 细胞 2(Th2)相关细胞因子参与大疱性类天疱疮(BP)的发病机制,这是一种自身免疫性皮肤病。在血清、皮肤活检和/或水疱液中观察到 Th2 细胞因子(如白细胞介素-4(IL-4)、IL-5、IL-6、IL-10 和 IL-13)的表达增加。本研究旨在探讨 Th2 细胞因子遗传变异与 BP 易感性之间的可能关联。
在一项队列研究中,收集 BP 患者和对照者的血液样本,并通过 PCR-RFLP 分析检测 IL-4(rs2243250 和 rs2070874)、IL-4R(rs1805010)、IL-5(rs2069812)、IL-6(rs1800795)、IL-10(rs1800896、rs1800871 和 rs1800872)和 IL-13(rs1800925 和 rs20541)的基因变异。此外,通过实时 RT-PCR 分析评估 IL-13 基因的定量表达水平。
在所研究的变异中,与 BP 患者相比,健康个体中 IL-13 基因变异(rs1800925)的 C 等位基因频率明显更高。这可能表明 C 等位基因对 BP 易感性具有保护作用。与野生基因型相比,考虑到携带多态性基因型的个体,IL-4R rs1805010 的小 G 等位基因和 IL-13 rs20541 的 A 等位基因分别对 BP 的发生具有促进和保护作用。在 BP 患者和健康个体之间未检测到 IL-13 mRNA 表达的显著差异。
我们的结果表明,IL-13 rs1800925 变异可能是 BP 发展的保护性遗传标志物。鉴于对 BP 的这种预防作用,潜在的治疗策略可以通过干扰 IL-13 细胞因子的功能来开发,该细胞因子似乎是嗜酸性炎症性疾病(如 BP)发病机制中的重要组成部分。