Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Pediatr Res. 2013 Nov;74(5):545-51. doi: 10.1038/pr.2013.134. Epub 2013 Aug 13.
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.
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.
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.
This study provides the first evidence supporting the association between TARC/CCL17 polymorphisms, susceptibility of KD, and IVIG responses in KD patients.
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。
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。
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。
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。