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白细胞介素-27 基因变异 rs153109 与伊朗人群中细胞因子血清水平升高和易感性增加有关。

Interleukin-27 gene variant rs153109 is associated with enhanced cytokine serum levels and susceptibility to Behçet's disease in the Iranian population.

机构信息

Autoimmune Diseases Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Department of Immunology, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Eur Cytokine Netw. 2020 Dec 1;31(4):140-146. doi: 10.1684/ecn.2020.0458.

Abstract

Behcet's disease (BD) is a systemic vasculitis, characterized by recurrent oral aphthous, genital ulcers, ocular lesions, and other organ involvement. Interleukin (IL)-27 with its pro- and anti-inflammatory effects might be an important effective cytokine in this disease. The aim of this study was to investigate the association of IL-27 serum concentration and a single-nucleotide polymorphism (SNP) rs153109 (-964 A > G) with the risk and clinical features of the patients with BD. IL-27 Genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and the IL-27 serum levels were measured using enzyme-linked immunosorbent assay (ELISA). It is shown that AG, GG, and AG + GG genotypes, as well as G allele of rs153109, can significantly increase the risk of BD in total and in male individuals. Significantly higher frequencies of AG and GG genotypes and G allele were observed in total and male patients with an active form of BD. AG and GG genotypes were associated with joint (p = 0.046) and vascular (p = 0.02) involvement. The frequency of the G allele was higher in all patients, as well as in female patients with vascular involvement (p = 0.02). Serum cytokine analysis indicated an increased level of IL-27 in BD patients compared to healthy subjects (p = 0.038). Additionally, a higher level of IL-27 was detected in patients carrying the rs153109 GG genotype (p = 0.04) and those with renal (p = 0.009) and skin (p = 0.05) involvement. In conclusion, this study underscores the involvement of IL-27 rs153109 variants and increased serum level in BD susceptibility and pathogenesis.

摘要

贝赫切特病(BD)是一种系统性血管炎,其特征为反复发作的口腔阿弗他溃疡、生殖器溃疡、眼部病变和其他器官受累。白细胞介素(IL)-27 及其促炎和抗炎作用可能是该病的重要有效细胞因子。本研究旨在探讨 IL-27 血清浓度和单核苷酸多态性(SNP)rs153109(-964A>G)与 BD 患者的风险和临床特征的关系。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对 IL-27 基因分型,采用酶联免疫吸附试验(ELISA)检测 IL-27 血清水平。结果表明,AG、GG 和 AG+GG 基因型以及 rs153109 的 G 等位基因可显著增加 BD 的总风险和男性个体的风险。在总患者和男性活动期 BD 患者中,AG 和 GG 基因型以及 G 等位基因的频率显著升高。AG 和 GG 基因型与关节(p=0.046)和血管(p=0.02)受累相关。在所有患者以及女性血管受累患者中,G 等位基因的频率更高(p=0.02)。血清细胞因子分析表明,BD 患者的 IL-27 水平高于健康对照者(p=0.038)。此外,在携带 rs153109 GG 基因型的患者(p=0.04)和肾(p=0.009)和皮肤(p=0.05)受累的患者中,检测到更高水平的 IL-27。综上所述,本研究强调了 IL-27 rs153109 变异和血清水平升高在 BD 易感性和发病机制中的作用。

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