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全基因组表达谱分析确定了急性川崎病的新治疗靶点。

Global gene expression profiling identifies new therapeutic targets in acute Kawasaki disease.

作者信息

Hoang Long Truong, Shimizu Chisato, Ling Ling, Naim Ahmad Nazri Mohamed, Khor Chiea Chuen, Tremoulet Adriana H, Wright Victoria, Levin Michael, Hibberd Martin L, Burns Jane C

机构信息

Genome Institute of Singapore, Singapore City, Singapore.

Department of Pediatrics, University of California San Diego and Rady Children's Hospital, La Jolla, CA 92093 USA.

出版信息

Genome Med. 2014 Nov 20;6(11):541. doi: 10.1186/s13073-014-0102-6. eCollection 2014.

Abstract

BACKGROUND

Global gene expression profiling can provide insight into the underlying pathophysiology of disease processes. Kawasaki disease (KD) is an acute, self-limited vasculitis whose etiology remains unknown. Although the clinical illness shares certain features with other pediatric infectious diseases, the occurrence of coronary artery aneurysms in 25% of untreated patients is unique to KD.

METHODS

To gain further insight into the molecular mechanisms underlying KD, we investigated the acute and convalescent whole blood transcriptional profiles of 146 KD subjects and compared them with the transcriptional profiles of pediatric patients with confirmed bacterial or viral infection, and with healthy control children. We also investigated the transcript abundance in patients with different intravenous immunoglobulin treatment responses and different coronary artery outcomes.

RESULTS

The overwhelming signature for acute KD involved signaling pathways of the innate immune system. Comparison with other acute pediatric infections highlighted the importance of pathways involved in cell motility including paxillin, relaxin, actin, integrins, and matrix metalloproteinases. Most importantly, the IL1β pathway was identified as a potential therapeutic target.

CONCLUSION

Our study revealed the importance of the IL-1 signaling pathway and a prominent signature of innate immunity and cell migration in the acute phase of the illness.

摘要

背景

全基因组表达谱分析有助于深入了解疾病过程的潜在病理生理学机制。川崎病(KD)是一种急性自限性血管炎,其病因尚不明确。尽管该临床疾病与其他儿科传染病有某些共同特征,但25%未经治疗的患者会出现冠状动脉瘤,这是KD独有的情况。

方法

为了进一步深入了解KD潜在的分子机制,我们研究了146例KD患者急性期和恢复期的全血转录谱,并将其与确诊为细菌或病毒感染的儿科患者以及健康对照儿童的转录谱进行比较。我们还研究了不同静脉注射免疫球蛋白治疗反应和不同冠状动脉结局患者的转录本丰度。

结果

急性KD的主要特征涉及先天免疫系统的信号通路。与其他急性儿科感染的比较突出了参与细胞运动的通路的重要性,包括桩蛋白、松弛素、肌动蛋白、整合素和基质金属蛋白酶。最重要的是,白细胞介素1β(IL1β)通路被确定为一个潜在的治疗靶点。

结论

我们的研究揭示了IL-1信号通路在疾病急性期的重要性以及先天免疫和细胞迁移的显著特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c87/4279699/55bbe68b5a2a/13073_2014_102_Fig1_HTML.jpg

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