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TARC/CCL17 基因多态性及其表达与川崎病易感性及冠状动脉瘤形成的关系。

TARC/CCL17 gene polymorphisms and expression associated with susceptibility and coronary artery aneurysm formation in Kawasaki disease.

机构信息

Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.

出版信息

Pediatr Res. 2013 Nov;74(5):545-51. doi: 10.1038/pr.2013.134. Epub 2013 Aug 13.

Abstract

BACKGROUND

Kawasaki disease (KD) is a systemic vasculitis of unknown etiology. Thymus and activation-regulated chemokine/chemokine ligand 17 (TARC/CCL17) is one of the Th2 chemokines and has been suggested as a candidate gene for conferring susceptibility to Th2 associated with allergy diseases. This study examined the correlation between gene polymorphisms and plasma levels of TARC/CCL17 in patients with KD and the outcomes of KD.

METHODS

A total of 381 KD patients and 564 controls were subjected to determination of five tagging single-nucleotide polymorphisms of TARC/CCL17. In addition, plasma TARC/CCL17 levels were measured by enzyme-linked immunosorbent assay.

RESULTS

Polymorphisms of TARC/CCL17 were significantly different between normal children and patients with KD. A allele of rs4784805 has better intravenous immunoglobulin (IVIG) treatment response to KD. Furthermore, plasma TARC/CCL17 levels were higher in KD patients than that in controls before IVIG treatment. After IVIG treatment, plasma TARC/CCL17 levels decreased significantly.

CONCLUSION

This study provides the first evidence supporting the association between TARC/CCL17 polymorphisms, susceptibility of KD, and IVIG responses in KD patients.

摘要

背景

川崎病(KD)是一种病因不明的全身血管炎。胸腺和激活调节趋化因子/趋化因子配体 17(TARC/CCL17)是一种 Th2 趋化因子,被认为是与过敏疾病相关的 Th2 易感性的候选基因。本研究探讨了 KD 患者 TARC/CCL17 基因多态性与血浆水平及其与 KD 结局的相关性。

方法

对 381 例 KD 患者和 564 例对照者进行 TARC/CCL17 五个标记单核苷酸多态性检测。同时,采用酶联免疫吸附试验测定血浆 TARC/CCL17 水平。

结果

TARC/CCL17 多态性在正常儿童和 KD 患者之间存在显著差异。rs4784805 的 A 等位基因对 KD 的静脉注射免疫球蛋白(IVIG)治疗反应更好。此外,KD 患者的血浆 TARC/CCL17 水平在 IVIG 治疗前高于对照组。IVIG 治疗后,血浆 TARC/CCL17 水平显著下降。

结论

本研究首次提供了证据支持 TARC/CCL17 多态性与 KD 易感性以及 KD 患者 IVIG 反应之间的关联。

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