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首页> 外文期刊>Archives of Dermatological Research >Genetic association of IFN-γ +874T/A polymorphism in Mexican patients with drug-induced Stevens-Johnson syndrome/toxic epidermal necrolysis
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Genetic association of IFN-γ +874T/A polymorphism in Mexican patients with drug-induced Stevens-Johnson syndrome/toxic epidermal necrolysis

机译:墨西哥药物诱发的史蒂文斯-约翰逊综合征/毒性表皮坏死患者中IFN-γ+ 874T / A多态性的遗传关联

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摘要

Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) are rare, but potentially life-threatening diseases, characterized by widespread epidermal necrosis and are predominantly drug induced. There is a paucity of data regarding the role of cytokine and cytokine receptors polymorphisms in the pathoimmunology of SJS/TEN. The aim of this study was to investigate the role of TNF-α-308, IFN-γ +874, IL-10-1082, IL-13 Arg130Gln, and IL-4R Gln551Arg gene polymorphisms in SJS/TEN in Mexican Mestizo patients. Twenty-nine unrelated SJS/TEN patients and 128 unrelated healthy individuals were studied. Genomic extraction was carried out from complete blood samples using the salting out method. The PCR–RFLP method was used to amplify the following polymorphisms: TNF-α-308, IFN-γ +874, IL-10-1082, IL-13 Arg130Gln, and IL-4R Gln551Arg. TNF-α-308, IL-10-1082, IL-13 Arg130Gln, and IL-4R Gln551Arg polymorphisms were not associated with the genetic susceptibility to SJS/TEN. The distribution of TT, TA, AA genotypes of IFN-γ +874 was significantly different in SJS/TEN patients compared with controls (pC = 0.012). TA and AA genotypes were grouped to highlight the differences between patients and controls given by the absence of the AA genotype in the group of patients (pC = 0.03, OR = 3.61 95 % CI 1.20–11.6). This preliminary study suggests that IFN-γ +874 T/A polymorphism is associated with SJS/TEN.
机译:史蒂文斯-约翰逊综合症/中毒性表皮坏死症(SJS / TEN)罕见,但具有潜在的威胁生命的疾病,其特征是广泛的表皮坏死,并且主要是药物诱发的。关于细胞因子和细胞因子受体多态性在SJS / TEN的病理免疫中的作用的数据很少。这项研究的目的是调查墨西哥Mestizo患者SJS / TEN中TNF-α-308,IFN-γ+ 874,IL-10-1082,IL-13 Arg130Gln和IL-4R Gln551Arg基因多态性的作用。研究了29名无关的SJS / TEN患者和128名无关的健康个体。使用盐析法从全血样本中提取基因组。 PCR-RFLP方法用于扩增以下多态性:TNF-α-308,IFN-γ+ 874,IL-10-1082,IL-13 Arg130Gln和IL-4R Gln551Arg。 TNF-α-308,IL-10-1082,IL-13 Arg130Gln和IL-4R Gln551Arg多态性与SJS / TEN的遗传易感性无关。 SJS / TEN患者的IFN-γ+874 TT,TA,AA基因型分布与对照组相比有显着差异(pC = 0.012)。 TA和AA基因型被分组以突出显示患者与对照组之间的差异,这是由于患者组中缺乏AA基因型所致(pC = 0.03,OR = 3.61 95%CI 1.20-11.6)。这项初步研究表明,IFN-γ+874 T / A多态性与SJS / TEN有关。

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  • 来源
    《Archives of Dermatological Research》 |2013年第4期|353-357|共5页
  • 作者单位

    Department of Dermatology Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán">(1);

    Department of Immunology and Rheumatology Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán">(2);

    Department of Immunology and Rheumatology Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán">(2);

    Department of Pathology Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán">(3);

    Department of Dermatology Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán">(1);

    Department of Immunology and Rheumatology Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán">(2);

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Stevens-Johnson syndrome; Toxic epidermal necrolysis; Interferon-γ polymorphisms;

    机译:史蒂文斯-约翰逊综合症;有毒的表皮坏死溶解;干扰素-γ多态性;

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