干扰素和 TLR3 基因的变异可能与系统性红斑狼疮的易感性及其临床表现有关。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
E. Modzelewska , A. Wajda , A. Lutkowska , A. Felis-Giemza , B. Stypińska , A. Matusiewicz , M. Puszczewicz , D. Majewski , P.P. Jagodziński , E. Haładyj , A. Paradowska-Gorycka
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引用次数: 0

摘要

该研究旨在探讨 IFN-α、IFN-β1、IFN-γ 和 TLR3 基因中的 10 个多态性对系统性红斑狼疮表型和易感性的潜在影响,并研究特定基因型与临床之间的关系。研究人员采集了系统性红斑狼疮患者和健康对照者的全血样本。用 QIAamp DNA 血液迷你试剂盒(Qiagen)从外周血中提取 DNA。分离出的 DNA 的质量和数量由 Quawell Q5000 分光光度计进行评估。我们使用实时 PCR(QuantStudio 5 thermocycler)对系统性红斑狼疮患者和健康人进行了基因分型。研究表明,IFN-γ rs2069705、IFN-γ rs2069718 和 IFN-α rs3758236 多态性在系统性红斑狼疮中具有保护作用。我们观察到 TLR3 rs3775292、IFN-β1 rs7873167、IFN-γ rs2069705、TLR3 rs3775291 和 TLR3 rs5743305 多态性与系统性红斑狼疮患者临床表现之间的关系。我们发现 IFN-α rs3758236、IFN-γ rs2069705、IFN-γ rs2069718、IFN-γ rs1861493 和 IFN-β1 rs10964831 多态性与系统性红斑狼疮和/或其合并症的临床表现之间存在关联。我们发现了 IFN-γ rs2069705、IFN-γ rs2069718、IFN-γ rs1861493、TLR3 rs3775291、TLR3 rs3775292 和 TLR3 rs5743305 多态性与自身抗体发生之间的联系。我们的研究揭示了 IFN 和 TLR 基因多态性与系统性红斑狼疮易感性、表型和自身抗体谱之间的关系。本研究认为,干扰素和TLR3基因的多态性可能与系统性红斑狼疮的发病机制和病程有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variations in the interferon and TLR3 genes may be associated with susceptibility to systemic lupus erythematosus and its clinical presentation

The study aimed to explore the pontential impact of 10 polymorphisms within IFN-α, IFN-β1, IFN-γ and TLR3 genes on SLE phenotype and susceptibility and to study the relationship between specific genotypes and clinics. Whole blood samples from SLE patients and healthy controls was obtained. DNA was extracted from the peripheral blood by the QIAamp DNA Blood Mini Kit (Qiagen). The quality and quantity of isolated DNA was estimated by the Quawell Q5000 spectrophotometer. We genotyped SLE patients and healthy subjects using real-time PCR (QuantStudio 5 thermocycler). The study suggests that IFN-γ rs2069705, IFN-γ rs2069718 and IFN-α rs3758236 polymorphisms have a protective role in SLE. We observed relations between TLR3 rs3775292, IFN-β1 rs7873167, IFN-γ rs2069705, TLR3 rs3775291 and TLR3 rs5743305 polymorphisms and clinical picture of SLE patients. We found associations between the IFN-α rs3758236, IFN-γ rs2069705, IFN-γ rs2069718, IFN-γ rs1861493 and IFN-β1 rs10964831 polymorphisms and the clinical manifestation of the SLE and/or its comorbidities. We perceived links between IFN-γ rs2069705, IFN-γ rs2069718, IFN-γ rs1861493, TLR3 rs3775291, TLR3 rs3775292 and TLR3 rs5743305 polymorphisms and the occurrence of autoantibodies. Our study presented the relationship between IFN and TLR gene polymorphisms with SLE susceptibility, phenotype and autoantibodies profile. This study propose that polymorphisms within interferons and TLR3 genes can be engaged in the SLE pathogenesis and course.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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