Policing the intestinal epithelial barrier: Innate immune functions of intraepithelial lymphocytes.

Q1 Medicine Current Pathobiology Reports Pub Date : 2018-03-01 Epub Date: 2018-01-15
Madeleine D Hu, Luo Jia, Karen L Edelblum
{"title":"Policing the intestinal epithelial barrier: Innate immune functions of intraepithelial lymphocytes.","authors":"Madeleine D Hu,&nbsp;Luo Jia,&nbsp;Karen L Edelblum","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose of review: </strong>This review will explore the contribution of IELs to mucosal innate immunity and highlight the similarities in IEL functional responses to bacteria, viruses and protozoan parasite invasion.</p><p><strong>Recent findings: </strong>IELs rapidly respond to microbial invasion by activating host defense responses, including the production of mucus and antimicrobial peptides to prevent microbes from reaching the epithelial surface. During active infection, IELs promote epithelial cytolysis, cytokine and chemokine production to limit pathogen invasion, replication and dissemination. Commensal-induced priming of IEL effector function or continuous surveillance of the epithelium may be important contributing factors to the rapidity of response.</p><p><strong>Summary: </strong>Impaired microbial recognition, dysregulated innate immune signaling or microbial dysbiosis may limit the protective function of IELs and increase susceptibility to disease. Further understanding of the mechanisms regulating IEL surveillance and sentinel function may provide insight into the development of more effective targeted therapies designed to reinforce the mucosal barrier.</p>","PeriodicalId":37014,"journal":{"name":"Current Pathobiology Reports","volume":" ","pages":"35-46"},"PeriodicalIF":0.0000,"publicationDate":"2018-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943048/pdf/nihms935041.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Pathobiology Reports","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/1/15 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose of review: This review will explore the contribution of IELs to mucosal innate immunity and highlight the similarities in IEL functional responses to bacteria, viruses and protozoan parasite invasion.

Recent findings: IELs rapidly respond to microbial invasion by activating host defense responses, including the production of mucus and antimicrobial peptides to prevent microbes from reaching the epithelial surface. During active infection, IELs promote epithelial cytolysis, cytokine and chemokine production to limit pathogen invasion, replication and dissemination. Commensal-induced priming of IEL effector function or continuous surveillance of the epithelium may be important contributing factors to the rapidity of response.

Summary: Impaired microbial recognition, dysregulated innate immune signaling or microbial dysbiosis may limit the protective function of IELs and increase susceptibility to disease. Further understanding of the mechanisms regulating IEL surveillance and sentinel function may provide insight into the development of more effective targeted therapies designed to reinforce the mucosal barrier.

Abstract Image

Abstract Image

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
维持肠上皮屏障:上皮内淋巴细胞的先天免疫功能。
综述目的:本文将探讨IEL对粘膜先天免疫的贡献,并强调IEL对细菌、病毒和原生动物寄生虫入侵的功能反应的相似性。最近的研究发现:IELs通过激活宿主防御反应,包括产生粘液和抗菌肽来阻止微生物到达上皮表面,从而对微生物入侵做出快速反应。在活动性感染期间,IELs促进上皮细胞溶解、细胞因子和趋化因子的产生,以限制病原体的入侵、复制和传播。评论诱导的IEL效应功能的启动或对上皮的持续监测可能是反应迅速的重要因素。微生物识别受损、先天免疫信号失调或微生物生态失调可能限制IELs的保护功能并增加对疾病的易感性。进一步了解IEL监测和前哨功能的调节机制可能有助于开发更有效的靶向治疗,以加强粘膜屏障。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Current Pathobiology Reports
Current Pathobiology Reports Medicine-Pathology and Forensic Medicine
CiteScore
6.40
自引率
0.00%
发文量
3
期刊介绍: This journal aims to offer expert review articles on the most important recent research pertaining to biological mechanisms underlying disease, including etiology, pathogenesis, and the clinical manifestations of cellular alteration. By providing clear, insightful, balanced contributions, the journal intends to serve those for whom the elucidation of new techniques and technologies related to pathobiology is essential. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas across the field. Section Editors select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An Editorial Board of more than 20 internationally diverse members reviews the annual table of contents, ensures that topics include emerging research, and suggests topics of special importance to their country/region. Topics covered may include autophagy, cancer stem cells, induced pluripotential stem cells (iPS cells), inflammation and cancer, matrix pathobiology, miRNA in pathobiology, mitochondrial dysfunction/diseases, and myofibroblast.
期刊最新文献
LRP1 in the Vascular Wall Dynamics and Sensitivity of Signaling Pathways. Platelet-Neutrophil Interactions and Thrombo-inflammatory Complications in Type 2 Diabetes Mellitus Role of Nanoscale Delivery Systems in Tissue Engineering Magnetic Nanostructures for Cancer Theranostic Applications
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1