浆细胞样树突状细胞降低i型干扰素与学龄期儿童哮喘的关系。

IF 12 1区 医学 Q1 ALLERGY
Allergy Pub Date : 2025-08-13 DOI:10.1111/all.70005
Isabelle Coenen,Anya C Jones,Alice A White,Mari Takashima,Wen Ray Lee,Matthew D Wong,Dwan Vilcins,Ulrich Kadolsky,Ali Sadiq Cheema,Alka Saxena,Anthony Bosco,Keith Grimwood,Peter D Sly,Deborah H Strickland,Jonatan Leffler
{"title":"浆细胞样树突状细胞降低i型干扰素与学龄期儿童哮喘的关系。","authors":"Isabelle Coenen,Anya C Jones,Alice A White,Mari Takashima,Wen Ray Lee,Matthew D Wong,Dwan Vilcins,Ulrich Kadolsky,Ali Sadiq Cheema,Alka Saxena,Anthony Bosco,Keith Grimwood,Peter D Sly,Deborah H Strickland,Jonatan Leffler","doi":"10.1111/all.70005","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nAllergic sensitization and reduced ability to respond to viral infections may contribute to virus-induced wheeze and asthma development in young children. Plasmacytoid dendritic cells (pDC) are rare immune cells that produce type I interferons (IFN-I) and play a key role in orchestrating immune responses against viruses.\r\n\r\nOBJECTIVE\r\nTo further evaluate the function of pDC in children with asthma.\r\n\r\nMETHODS\r\nThis study was based on a subset of 71 children from the Early Life Lung Function (ELLF) cohort at the age of 7 years. As part of the ELLF study, participants were characterized for atopic sensitization, viral infection history, and lung function testing. pDC responses to a TLR7/8 agonist were assessed in the presence or absence of anti-IgE using an in vitro assay. Responses were evaluated utilizing flow cytometry, multiplexed cytokine assays, and transcriptional analysis of isolated pDC.\r\n\r\nRESULTS\r\npDC responses varied considerably across individuals, and those who responded with IFN-I following stimulation showed a lower proportion of asthma compared to those who responded with TNF-only. A TNF-only response was associated with increased atopy and reduced upregulation of IFN-associated genes. Anti-IgE stimulation reduced pDC activation, and the reduction was associated with baseline expression of the IgE receptor (FcεR1). A reduction in a gene module centralized around genes such as TPM2, LILRA4, and CLEC4C was also observed.\r\n\r\nCONCLUSION\r\nTogether, these findings suggest that pDC responses are variable, associated with asthma, and appear influenced by environmental stimuli. This response thus appears to be an important aspect of asthma pathology in children.","PeriodicalId":122,"journal":{"name":"Allergy","volume":"1 1","pages":""},"PeriodicalIF":12.0000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reduced Type-I Interferon by Plasmacytoid Dendritic Cells and Asthma in School-Aged Children.\",\"authors\":\"Isabelle Coenen,Anya C Jones,Alice A White,Mari Takashima,Wen Ray Lee,Matthew D Wong,Dwan Vilcins,Ulrich Kadolsky,Ali Sadiq Cheema,Alka Saxena,Anthony Bosco,Keith Grimwood,Peter D Sly,Deborah H Strickland,Jonatan Leffler\",\"doi\":\"10.1111/all.70005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND\\r\\nAllergic sensitization and reduced ability to respond to viral infections may contribute to virus-induced wheeze and asthma development in young children. Plasmacytoid dendritic cells (pDC) are rare immune cells that produce type I interferons (IFN-I) and play a key role in orchestrating immune responses against viruses.\\r\\n\\r\\nOBJECTIVE\\r\\nTo further evaluate the function of pDC in children with asthma.\\r\\n\\r\\nMETHODS\\r\\nThis study was based on a subset of 71 children from the Early Life Lung Function (ELLF) cohort at the age of 7 years. As part of the ELLF study, participants were characterized for atopic sensitization, viral infection history, and lung function testing. pDC responses to a TLR7/8 agonist were assessed in the presence or absence of anti-IgE using an in vitro assay. Responses were evaluated utilizing flow cytometry, multiplexed cytokine assays, and transcriptional analysis of isolated pDC.\\r\\n\\r\\nRESULTS\\r\\npDC responses varied considerably across individuals, and those who responded with IFN-I following stimulation showed a lower proportion of asthma compared to those who responded with TNF-only. A TNF-only response was associated with increased atopy and reduced upregulation of IFN-associated genes. Anti-IgE stimulation reduced pDC activation, and the reduction was associated with baseline expression of the IgE receptor (FcεR1). A reduction in a gene module centralized around genes such as TPM2, LILRA4, and CLEC4C was also observed.\\r\\n\\r\\nCONCLUSION\\r\\nTogether, these findings suggest that pDC responses are variable, associated with asthma, and appear influenced by environmental stimuli. This response thus appears to be an important aspect of asthma pathology in children.\",\"PeriodicalId\":122,\"journal\":{\"name\":\"Allergy\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":12.0000,\"publicationDate\":\"2025-08-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Allergy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/all.70005\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ALLERGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Allergy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/all.70005","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:过敏致敏和对病毒感染的反应能力降低可能是幼儿病毒诱导的喘息和哮喘发展的原因。浆细胞样树突状细胞(pDC)是一种罕见的产生I型干扰素(IFN-I)的免疫细胞,在协调针对病毒的免疫反应中发挥关键作用。目的进一步评价儿童哮喘中pDC的功能。方法:本研究基于71名7岁早期生命肺功能(ELLF)队列的儿童。作为ELLF研究的一部分,参与者进行了特应性致敏、病毒感染史和肺功能测试。使用体外实验评估pDC对TLR7/8激动剂的反应,无论是否存在抗ige。利用流式细胞术、多重细胞因子测定和分离的pDC转录分析来评估反应。结果不同个体的spdc反应差异很大,与仅接受tnf治疗的患者相比,在刺激后接受IFN-I治疗的患者哮喘比例较低。仅tnf反应与特异性增加和ifn相关基因上调减少有关。抗IgE刺激降低了pDC的活化,这种降低与IgE受体(FcεR1)的基线表达有关。还观察到集中在TPM2、LILRA4和CLEC4C等基因周围的基因模块的减少。综上所述,这些发现表明,pDC反应是可变的,与哮喘有关,并可能受到环境刺激的影响。因此,这种反应似乎是儿童哮喘病理的一个重要方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced Type-I Interferon by Plasmacytoid Dendritic Cells and Asthma in School-Aged Children.
BACKGROUND Allergic sensitization and reduced ability to respond to viral infections may contribute to virus-induced wheeze and asthma development in young children. Plasmacytoid dendritic cells (pDC) are rare immune cells that produce type I interferons (IFN-I) and play a key role in orchestrating immune responses against viruses. OBJECTIVE To further evaluate the function of pDC in children with asthma. METHODS This study was based on a subset of 71 children from the Early Life Lung Function (ELLF) cohort at the age of 7 years. As part of the ELLF study, participants were characterized for atopic sensitization, viral infection history, and lung function testing. pDC responses to a TLR7/8 agonist were assessed in the presence or absence of anti-IgE using an in vitro assay. Responses were evaluated utilizing flow cytometry, multiplexed cytokine assays, and transcriptional analysis of isolated pDC. RESULTS pDC responses varied considerably across individuals, and those who responded with IFN-I following stimulation showed a lower proportion of asthma compared to those who responded with TNF-only. A TNF-only response was associated with increased atopy and reduced upregulation of IFN-associated genes. Anti-IgE stimulation reduced pDC activation, and the reduction was associated with baseline expression of the IgE receptor (FcεR1). A reduction in a gene module centralized around genes such as TPM2, LILRA4, and CLEC4C was also observed. CONCLUSION Together, these findings suggest that pDC responses are variable, associated with asthma, and appear influenced by environmental stimuli. This response thus appears to be an important aspect of asthma pathology in children.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Allergy
Allergy 医学-过敏
CiteScore
26.10
自引率
9.70%
发文量
393
审稿时长
2 months
期刊介绍: Allergy is an international and multidisciplinary journal that aims to advance, impact, and communicate all aspects of the discipline of Allergy/Immunology. It publishes original articles, reviews, position papers, guidelines, editorials, news and commentaries, letters to the editors, and correspondences. The journal accepts articles based on their scientific merit and quality. Allergy seeks to maintain contact between basic and clinical Allergy/Immunology and encourages contributions from contributors and readers from all countries. In addition to its publication, Allergy also provides abstracting and indexing information. Some of the databases that include Allergy abstracts are Abstracts on Hygiene & Communicable Disease, Academic Search Alumni Edition, AgBiotech News & Information, AGRICOLA Database, Biological Abstracts, PubMed Dietary Supplement Subset, and Global Health, among others.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信