首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Association of functional polymorphisms in promoter regions of IL5, IL6 and IL13 genes with development and prognosis of autoimmune thyroid diseases.
【24h】

Association of functional polymorphisms in promoter regions of IL5, IL6 and IL13 genes with development and prognosis of autoimmune thyroid diseases.

机译:IL5,IL6和IL13基因启动子区域的功能多态性与自身免疫性甲状腺疾病的发展和预后的关系。

获取原文
获取原文并翻译 | 示例
           

摘要

To clarify the association of genetic producibility of interleukin (IL)-5, IL-6 and IL-13, which are secreted by T helper type 2 (Th2), with the development and prognosis of autoimmune thyroid disease (AITD), we genotyped IL5-746C/T, IL6-572C/G and IL13-1112C/T polymorphisms, which are functional polymorphisms in the promoter regions of the genes regulating these cytokines. Fifty-seven patients with intractable Graves' disease (GD), 52 with GD in remission, 52 with severe Hashimoto's disease (HD), 56 with mild HD and 91 healthy controls were examined in this study. The IL13-1112T allele, which correlates with higher producibility of IL-13, was more frequent in patients with GD in remission than in those with intractable GD [P=0.009, odds ratio (OR)=3.52]. The IL5-746T allele, which may correlate with lower levels of IL-5, was more frequent in patients with GD in remission than controls (P=0.029, OR=2.00). The IL6-572G allele carriers (CG and GG genotypes), which have higher producibility of IL-6, were more frequent in AITD patients (P=0.033, OR=1.75), especially in GD in remission (P=0.031, OR=2.16) and severe HD (P=0.031, OR=2.16) than in controls. Interestingly, both allele and genotype frequencies of Th2 cytokine genes were similar between GD and HD patients. In conclusion, functional polymorphisms in the genes encoding Th2 cytokines are associated differently with the development and prognosis of AITD from each other.
机译:为了阐明由2型T辅助细胞(Th2)分泌的白介素(IL)-5,IL-6和IL-13的遗传可生产性与自身免疫性甲状腺疾病(AITD)的发展和预后的关系,我们进行了基因分型IL5-746C / T,IL6-572C / G和IL13-1112C / T多态性,它们是调节这些细胞因子的基因的启动子区域中的功能性多态性。本研究共检查了57例难治性Graves病(GD),52例GD缓解,52例重度桥本氏病(HD),56例轻度HD和91例健康对照者。与患有顽固性GD的患者相比,具有缓解的GD患者中IL13-1112T等位基因与IL-13的更高生产相关[P = 0.009,优势比(OR)= 3.52]。 GD缓解患者中的IL5-746T等位基因可能与较低的IL-5水平相关(P = 0.029,OR = 2.00)。 IL6-572G等位基因携带者(CG和GG基因型),具有更高的IL-6产生率,在AITD患者中更为频繁(P = 0.033,OR = 1.75),尤其是在GD缓解期(P = 0.031,OR = 2.16)和严重HD(P = 0.031,OR = 2.16)。有趣的是,GD和HD患者之间Th2细胞因子基因的等位基因和基因型频率相似。总之,编码Th2细胞因子的基因中的功能多态性彼此之间与AITD的发生和预后不同。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号