Association between TLR-2 and TLR-9 gene polymorphisms (rs5743708 and rs5743836) and susceptibility to psoriatic arthritis in Egyptian patients.

Nora E Abdelbaset, Sahar S Khattab, Nashwa M Abd Elbaky, Basma M Elnaggar, Sara A Galal
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Abstract

Psoriasis (PsO) is a chronic immune-mediated disease of the skin. Psoriatic arthritis (PsA) is a prevalent chronic inflammatory disease that is associated with joint destruction and disability. The presence of PsO is the single greatest risk factor for the development of PsA. Toll-like receptors (TLRs) are trans-membrane proteins coded by the toll genes family. They are expressed in different cell types including immune and non-immune cells. Polymorphisms in TLR genes that lead to changes in these receptors or interfere with the transcription rates of their messenger ribonucleic acid (mRNA), may be involved in the chronic inflammatory immune response observed in PsA. This study involved 50 patients with PsA, 50 patients with cutaneous PsO and 50 age and sex matched normal subjects as controls. We aimed to assess TLR-2 (rs5743708) and TLR-9 (rs5743836) gene polymorphisms as potential risk factors for PsA in Egyptian patients with cutaneous PsO. Genotyping and allele frequencies were performed using Real Time polymerase chain reaction (qRT-PCR). Toll-like receptor-2 (TLR-2) rs5743708 and TLR-9 rs5743836 polymorphisms were associated with increased risk of PsO as an autoimmune disease, however they were not related to increase susceptibility to PsA in this cohort study of Egyptian patients.

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TLR-2和TLR-9基因多态性(rs5743708和rs5743836)与埃及患者银屑病关节炎易感性的关系
牛皮癣(PsO)是一种慢性免疫介导的皮肤疾病。银屑病关节炎(PsA)是一种常见的慢性炎症性疾病,与关节破坏和残疾有关。PsO的存在是PsA发展的最大危险因素。toll样受体(TLRs)是由toll基因家族编码的跨膜蛋白。它们在不同的细胞类型中表达,包括免疫细胞和非免疫细胞。TLR基因的多态性导致这些受体的改变或干扰其信使核糖核酸(mRNA)的转录率,可能参与PsA中观察到的慢性炎症免疫反应。本研究涉及50例PsA患者,50例皮肤PsO患者和50例年龄和性别匹配的正常受试者作为对照。我们旨在评估TLR-2 (rs5743708)和TLR-9 (rs5743836)基因多态性作为埃及皮肤PsO患者PsA的潜在危险因素。采用实时聚合酶链反应(Real Time polymerase chain reaction, qRT-PCR)进行基因分型和等位基因频率分析。toll样受体-2 (TLR-2) rs5743708和TLR-9 rs5743836多态性与PsO作为自身免疫性疾病的风险增加相关,但在埃及患者的队列研究中,它们与PsA易感性增加无关。
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CiteScore
1.20
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52
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