A model of dysregulated crosstalk between dendritic, natural killer, and regulatory T cells in chronic obstructive pulmonary disease

IF 13.1 1区 医学 Q1 IMMUNOLOGY Trends in Immunology Pub Date : 2024-05-18 DOI:10.1016/j.it.2024.04.010
Dawit T. Mengistu, Jeffrey L. Curtis, Christine M. Freeman
{"title":"A model of dysregulated crosstalk between dendritic, natural killer, and regulatory T cells in chronic obstructive pulmonary disease","authors":"Dawit T. Mengistu, Jeffrey L. Curtis, Christine M. Freeman","doi":"10.1016/j.it.2024.04.010","DOIUrl":null,"url":null,"abstract":"<p>Chronic obstructive pulmonary disease (COPD) is characterized by infiltration of the airways and lung parenchyma by inflammatory cells. Lung pathology results from the cumulative effect of complex and aberrant interactions between multiple cell types. However, three cell types, natural killer cells (NK), dendritic cells (DCs), and regulatory T cells (Tregs), are understudied and underappreciated. We propose that their mutual interactions significantly contribute to the development of COPD. Here, we highlight recent advances in NK, DC, and Treg biology with relevance to COPD, discuss their pairwise bidirectional interactions, and identify knowledge gaps that must be bridged to develop novel therapies. Understanding their interactions will be crucial for therapeutic use of autologous Treg, an approach proving effective in other diseases with immune components.</p>","PeriodicalId":54412,"journal":{"name":"Trends in Immunology","volume":"29 1","pages":""},"PeriodicalIF":13.1000,"publicationDate":"2024-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Trends in Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.it.2024.04.010","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Chronic obstructive pulmonary disease (COPD) is characterized by infiltration of the airways and lung parenchyma by inflammatory cells. Lung pathology results from the cumulative effect of complex and aberrant interactions between multiple cell types. However, three cell types, natural killer cells (NK), dendritic cells (DCs), and regulatory T cells (Tregs), are understudied and underappreciated. We propose that their mutual interactions significantly contribute to the development of COPD. Here, we highlight recent advances in NK, DC, and Treg biology with relevance to COPD, discuss their pairwise bidirectional interactions, and identify knowledge gaps that must be bridged to develop novel therapies. Understanding their interactions will be crucial for therapeutic use of autologous Treg, an approach proving effective in other diseases with immune components.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
慢性阻塞性肺病中树突状细胞、自然杀伤细胞和调节性 T 细胞之间失调的串扰模型
慢性阻塞性肺病(COPD)的特点是气道和肺实质被炎症细胞浸润。肺部病变是多种细胞类型之间复杂而异常的相互作用累积效应的结果。然而,自然杀伤细胞(NK)、树突状细胞(DCs)和调节性 T 细胞(Tregs)这三种细胞类型却未得到充分研究和重视。我们认为,它们之间的相互作用对慢性阻塞性肺病的发病有重要影响。在此,我们将重点介绍与慢性阻塞性肺病相关的 NK、DC 和 Treg 生物学的最新进展,讨论它们之间成对的双向相互作用,并找出开发新型疗法必须弥合的知识差距。了解它们之间的相互作用对自体Treg的治疗使用至关重要,这种方法已被证明对其他具有免疫成分的疾病有效。
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
Trends in Immunology
Trends in Immunology 医学-免疫学
CiteScore
25.10
自引率
0.60%
发文量
130
审稿时长
6-12 weeks
期刊介绍: Trends in Immunology serves as a vital platform for tracking advancements across various areas of immunology, offering concise reviews and hypothesis-driven viewpoints in each issue. With additional sections providing comprehensive coverage, the journal offers a holistic view of immunology. This broad perspective makes it an invaluable resource for researchers, educators, and students, facilitating the connection between basic and clinical immunology. Recognized as one of the top monthly review journals in its field, Trends in Immunology is highly regarded by the scientific community.
期刊最新文献
SARS-CoV-2 reprograms murine alveolar macrophages to dampen flu. Enhancing tumor immunity via in vivo cDC1 reprogramming. The peptide selectivity model: Interpreting NK cell KIR-HLA-I binding interactions and their associations to human diseases. Weapon of choice: viruses share cross-kingdom tools. Nanotube-mediated mitochondrial transfer: power to the T cells!
×
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