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病毒感染后喘息患儿 CDHR3 表达降低。

Reduced CDHR3 expression in children wheezing with rhinovirus.

机构信息

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Pediatr Allergy Immunol. 2018 Mar;29(2):200-206. doi: 10.1111/pai.12858.

Abstract

BACKGROUND

Rhinovirus-induced wheezing in young children has been associated with increased asthma risk at school age. Recently, the transmembrane protein cadherin-related family member 3 (CDHR3) was identified as the RV-C receptor and the genetic variant rs6967330 (p.Cys529Tyr) was reported to be associated with enhanced RV-C binding and increased replication in vitro. The aim of this study was to examine rs6967330 genotypes and mRNA expression of CDHR3 in relation to presence of rhinovirus and clinical symptoms in children with acute wheezing and compare to a group of age-matched healthy children.

METHODS

rs6967330;G>A was genotyped (n = 216), and CDHR3 mRNA expression was measured in peripheral blood leukocytes (n = 69) from a subgroup of children wheezing with RV infection acute and at a follow-up visit 2-3 months later, and in healthy controls. Standardized TaqMan assays were used.

RESULTS

The risk allele rs6967330-A was over-represented in the wheezing group (P < .001). Reduced mRNA levels of CDHR3 were found in children with acute wheezing as compared to the control group (P = .001). Children with the rs6967330 genotypes AA/AG showed the largest differences in CDHR3 expression between acute and follow-up visit (P < .04).

CONCLUSIONS

Preschool children with RV-induced wheezing were shown to have reduced CDHR3 mRNA levels, which might result in an increased permeability of the epithelial layers of the airways and thereby an increased vulnerability. Thus, measuring CDHR3 mRNA levels might help to identify a more severe phenotype of wheezing preschool children.

摘要

背景

鼻病毒诱发的幼儿喘息与学龄期哮喘风险增加有关。最近,跨膜蛋白钙黏蛋白相关家族成员 3(CDHR3)被鉴定为 RV-C 受体,遗传变异 rs6967330(p.Cys529Tyr)被报道与增强的 RV-C 结合和体外复制增加有关。本研究旨在检测急性喘息儿童中 rs6967330 基因型和 CDHR3 mRNA 表达与鼻病毒存在及临床症状的关系,并与年龄匹配的健康儿童进行比较。

方法

对 216 例儿童进行 rs6967330;G>A 基因型检测,对急性 RV 感染喘息和 2-3 个月后随访的儿童外周血白细胞中 CDHR3 mRNA 表达进行亚组测量,并与健康对照组进行比较。使用标准化 TaqMan 检测。

结果

喘息组风险等位基因 rs6967330-A 过度表达(P<.001)。与对照组相比,急性喘息儿童 CDHR3 mRNA 水平降低(P=.001)。与急性组相比,rs6967330 基因型 AA/AG 的儿童 CDHR3 表达差异最大(P<.04)。

结论

RV 诱导喘息的学龄前儿童表现出 CDHR3 mRNA 水平降低,这可能导致气道上皮层通透性增加,从而增加易感性。因此,测量 CDHR3 mRNA 水平可能有助于识别更严重的学龄前儿童喘息表型。

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