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首页> 外文期刊>Clinical and experimental dermatology >Inducible T‐cell costimulator ( ICOS ICOS ICOS ) and CD 28 CD CD 28 polymorphisms possibly play a role in the pathogenesis of chronic autoreactive urticaria
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Inducible T‐cell costimulator ( ICOS ICOS ICOS ) and CD 28 CD CD 28 polymorphisms possibly play a role in the pathogenesis of chronic autoreactive urticaria

机译:诱导型T细胞共刺激器(ICOS ICOS ICOS)和CD 28 CD 28多态性可能在慢性自身反应性荨麻疹的发病机制中发挥作用

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Summary Background Clinical experience emphasizes the coexistence of chronic spontaneous urticaria ( CSU ) and autoimmune disturbances. In chromosome 2q33‐34, there is a cluster of homologous genes that are considered promising candidate genes for susceptibility to autoimmune diseases. Aim To examine the possible role of polymorphisms in the genes for CD 28 and inducible T‐cell costimulator ( ICOS ) in the background of CSU . Methods In total, 149 patients with CSU with positive autologous serum skin test were enrolled in the study. The healthy control ( HC ) group consisted of 100 healthy volunteers. In all subjects, the CD 28 rs2140148 and rs3116496 and the ICOS rs6726035 polymorphisms were analysed. Disease severity was assessed by means of Urticaria Activity Score. Results We found a statistically significantly lower prevalence of the ICOS rs6726035 TT genotype among patients with CSU compared with HC s. Furthermore, the haplotype rs2140148A, rs3116496T and rs6726035C presented a possible association with CSU . We did not find any association between the examined polymorphisms and either urticaria severity or age of disease onset. Conclusions Our results underline the role of autoimmune components in the pathogenesis of chronic autoreactive urticaria, and indicate it as a potentially genetically related disorder.
机译:发明内容背景临床经验强调慢性自发性荨麻疹(CSU)和自身免疫扰动的共存。在染色体2Q33-34中,存在一组同源基因,被认为是对自身免疫疾病易感性的有希望的候选基因。目的在于CSU的背景下探讨多态性在CD 28和诱导型T细胞共刺激器(ICOS)的基因中的可能作用。研究总共149例CSU患者具有阳性自体血清皮肤试验的患者。健康对照(HC)组由100名健康志愿者组成。在所有科目中,分析了CD 28 RS2140148和RS3116496和ICOS RS6726035多态性。通过荨麻疹活动分数评估疾病严重程度。结果与HC S相比,我们发现患有CSU患者的ICOS RS6726035 TT基因型的统计上显着降低。此外,单倍型RS2140148A,RS3116496T和RS6726035C呈现了与CSU的可能关联。我们没有发现检测到的多态性和荨麻疹的荨麻疹严重程度或疾病年龄之间的任何关联。结论我们的结果强调了自身免疫组分在慢性自身反应性荨麻疹发病机制中的作用,并表明其作为潜在的转基因相关疾病。

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    Department of Internal Diseases Allergology and Clinical ImmunologyMedical University of;

    Department of Internal Diseases Diabetology and NephrologyMedical University of SilesiaKatowice;

    Department of Internal Diseases Diabetology and NephrologyMedical University of SilesiaKatowice;

    Department of Internal Diseases and NephrodiabetologyMedical University of LodzLodz Poland;

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  • 正文语种 eng
  • 中图分类 皮肤病学与性病学 ;
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