Suppr超能文献

鼠副流感病毒在肺固有免疫细胞中持续存在,维持慢性肺部病变。

Murine Parainfluenza Virus Persists in Lung Innate Immune Cells Sustaining Chronic Lung Pathology.

作者信息

Castro Ítalo Araujo, Yang Yanling, Gnazzo Victoria, Kim Do-Hyun, Van Dyken Steven J, López Carolina B

机构信息

Department of Molecular Microbiology and Center for Womeńs Infectious Diseases Research, Washington University School of Medicine, Saint Louis, Missouri, USA.

Department of Pathology & Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.

出版信息

bioRxiv. 2023 Nov 8:2023.11.07.566103. doi: 10.1101/2023.11.07.566103.

Abstract

Respiratory viruses including the human parainfluenza viruses (hPIVs) are a constant burden to human health, with morbidity and mortality frequently increased after the acute phase of the infection. Although is proven that respiratory viruses can persist , the mechanisms of virus or viral products persistence, their sources, and their impact on chronic respiratory diseases are unknown. Here, we used Sendai virus (SeV) to model hPIV infection in mice and test whether virus persistence associates with the development of chronic lung disease. Following SeV infection, virus products were detected in lung macrophages, type 2 innate lymphoid cells (ILC2s) and dendritic cells for several weeks after the infectious virus was cleared. Cells containing viral protein showed strong upregulation of antiviral and type 2 inflammation-related genes that associate with the development of chronic post-viral lung diseases, including asthma. Lineage tracing of infected cells or cells derived from infected cells suggests that distinct functional groups of cells contribute to the chronic pathology. Importantly, targeted ablation of infected cells or those derived from infected cells significantly ameliorated chronic lung disease. Overall, we identified persistent infection of innate immune cells as a critical factor in the progression from acute to chronic post viral respiratory disease.

摘要

包括人副流感病毒(hPIVs)在内的呼吸道病毒一直是人类健康的负担,感染急性期过后,发病率和死亡率常常会升高。尽管已证实呼吸道病毒能够持续存在,但其持续存在的机制、来源及其对慢性呼吸道疾病的影响尚不清楚。在此,我们利用仙台病毒(SeV)在小鼠中模拟hPIV感染,并测试病毒持续存在是否与慢性肺病的发展相关。SeV感染后,在感染性病毒清除后的数周内,在肺巨噬细胞、2型固有淋巴细胞(ILC2s)和树突状细胞中检测到病毒产物。含有病毒蛋白的细胞显示出与慢性病毒后肺部疾病(包括哮喘)发展相关的抗病毒和2型炎症相关基因的强烈上调。对感染细胞或源自感染细胞的细胞进行谱系追踪表明,不同功能组的细胞导致了慢性病理。重要的是,对感染细胞或源自感染细胞的细胞进行靶向清除可显著改善慢性肺病。总体而言,我们确定固有免疫细胞的持续感染是从急性病毒后呼吸道疾病发展为慢性疾病的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/067e/10659393/af7ed904710f/nihpp-2023.11.07.566103v1-f0001.jpg

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