Suppr超能文献

白细胞介素-4基因(IL4)的一种常见单倍型与韩国儿童的严重呼吸道合胞病毒病相关。

A common haplotype of interleukin-4 gene IL4 is associated with severe respiratory syncytial virus disease in Korean children.

作者信息

Choi Eun Hwa, Lee Hoan Jong, Yoo Taiwoo, Chanock Stephen J

机构信息

Section of Genomic Variation, Pediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

J Infect Dis. 2002 Nov 1;186(9):1207-11. doi: 10.1086/344310. Epub 2002 Oct 11.

Abstract

Respiratory syncytial virus (RSV) is a major health problem in young children, and host response to severe disease favors a Th2 immune response. To investigate the genetic basis for RSV disease severity, linked variants of 3 Th2 cytokine genes, IL4, IL13, and IL5 (which are clustered on chromosome 5q31.1) were characterized in 105 children who were hospitalized with severe RSV infection and 315 Korean control subjects in a pilot study. A common IL4 haplotype defined at 5 loci, which includes the -589T promoter variant, previously shown to be associated with increased interleukin (IL)-4 transcriptional activity and predisposition to asthma, was overrepresented in patients with severe RSV disease (odds ratio, 1.63; P=.02). These results support the hypothesis that severe RSV disease might be related to increased Th2 response, which is perhaps mediated by overexpression of IL-4, and provide preliminary evidence for a genetic link between severe RSV disease and subsequent wheezing.

摘要

呼吸道合胞病毒(RSV)是幼儿健康的一个主要问题,宿主对严重疾病的反应倾向于Th2免疫反应。为了研究RSV疾病严重程度的遗传基础,在一项初步研究中,对105名因严重RSV感染住院的儿童和315名韩国对照受试者的3个Th2细胞因子基因IL4、IL13和IL5(它们聚集在5号染色体的5q31.1上)的连锁变异进行了特征分析。在5个位点定义的一种常见的IL4单倍型,包括-589T启动子变体,先前已证明其与白细胞介素(IL)-4转录活性增加和哮喘易感性相关,在患有严重RSV疾病的患者中过度存在(优势比,1.63;P=0.02)。这些结果支持了这样一种假设,即严重的RSV疾病可能与Th2反应增加有关,这可能是由IL-4的过表达介导的,并为严重RSV疾病与随后的喘息之间的遗传联系提供了初步证据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验