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上呼吸道细胞转录组学在急性喘息的幼儿中确定了一种具有强临床相关性的主要新型免疫表型。

Upper Airway Cell Transcriptomics Identify a Major New Immunological Phenotype with Strong Clinical Correlates in Young Children with Acute Wheezing.

机构信息

Division of Cardiovascular and Respiratory Sciences, The University of Western Australia, Perth, Western Australia 6009, Australia.

Telethon Kids Institute, The University of Western Australia, Perth, Western Australia 6008, Australia.

出版信息

J Immunol. 2019 Mar 15;202(6):1845-1858. doi: 10.4049/jimmunol.1800178. Epub 2019 Feb 11.

Abstract

Asthma exacerbations are triggered by rhinovirus infections. We employed a systems biology approach to delineate upper-airway gene network patterns underlying asthma exacerbation phenotypes in children. Cluster analysis unveiled distinct IRF7 versus IRF7 molecular phenotypes, the former exhibiting robust upregulation of Th1/type I IFN responses and the latter an alternative signature marked by upregulation of cytokine and growth factor signaling and downregulation of IFN-γ. The two phenotypes also produced distinct clinical phenotypes. For IRF7 children, symptom duration prior to hospital presentation was more than twice as long from initial symptoms ( = 0.011) and nearly three times as long for cough ( < 0.001), the odds ratio of admission to hospital was increased more than 4-fold ( = 0.018), and time to recurrence was shorter ( = 0.015). In summary, our findings demonstrate that asthma exacerbations in children can be divided into IRF7 versus IRF7 phenotypes with associated differences in clinical phenotypes.

摘要

哮喘加重是由鼻病毒感染引发的。我们采用系统生物学方法来描绘儿童哮喘加重表型的上呼吸道基因网络模式。聚类分析揭示了 IRF7 与 IRF7 分子表型的不同,前者表现出 Th1/Ⅰ型 IFN 反应的强烈上调,后者则表现出以细胞因子和生长因子信号上调以及 IFN-γ下调为特征的替代特征。这两种表型还产生了不同的临床表型。对于 IRF7 儿童,从最初症状开始到住院就诊的症状持续时间是两倍以上( = 0.011),咳嗽时间几乎长三倍( < 0.001),住院的几率增加了 4 倍以上( = 0.018),复发时间更短( = 0.015)。总之,我们的研究结果表明,儿童哮喘加重可分为 IRF7 与 IRF7 表型,其临床表型存在差异。

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