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本文引用的文献

1
Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range.鼻腔黏膜中的免疫细胞居留可能部分解释了呼吸道疾病在整个年龄段的严重程度。
Sci Rep. 2021 Aug 5;11(1):15927. doi: 10.1038/s41598-021-95532-3.
2
Robust SARS-CoV-2 infection in nasal turbinates after treatment with systemic neutralizing antibodies.经系统中和抗体治疗后,鼻甲骨中出现稳健的 SARS-CoV-2 感染。
Cell Host Microbe. 2021 Apr 14;29(4):551-563.e5. doi: 10.1016/j.chom.2021.02.019. Epub 2021 Feb 25.
3
Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes.TNF-α 和 IFN-γ 的协同作用可引发 SARS-CoV-2 感染和细胞因子休克综合征中的炎症细胞死亡、组织损伤和死亡。
Cell. 2021 Jan 7;184(1):149-168.e17. doi: 10.1016/j.cell.2020.11.025. Epub 2020 Nov 19.
4
Distinct expression of SARS-CoV-2 receptor ACE2 correlates with endotypes of chronic rhinosinusitis with nasal polyps.SARS-CoV-2 受体 ACE2 的不同表达与鼻息肉慢性鼻窦炎的表型有关。
Allergy. 2021 Mar;76(3):789-803. doi: 10.1111/all.14665. Epub 2020 Nov 29.
5
Inflammatory endotypes of CRSwNP and responses to COVID-19.慢性鼻窦炎伴鼻息肉(CRSwNP)的炎症表型与对 COVID-19 的反应。
Curr Opin Allergy Clin Immunol. 2021 Feb 1;21(1):8-15. doi: 10.1097/ACI.0000000000000700.
6
The characterization of chronic rhinosinusitis in hospitalized patients with COVID-19.新冠病毒感染住院患者慢性鼻-鼻窦炎的特征
J Allergy Clin Immunol Pract. 2020 Nov-Dec;8(10):3597-3599.e2. doi: 10.1016/j.jaip.2020.09.013. Epub 2020 Sep 24.
7
Expression of ACE2 in airways: Implication for COVID-19 risk and disease management in patients with chronic inflammatory respiratory diseases.气道中 ACE2 的表达:对慢性炎症性呼吸道疾病患者 COVID-19 风险和疾病管理的影响。
Clin Exp Allergy. 2020 Dec;50(12):1313-1324. doi: 10.1111/cea.13746. Epub 2020 Oct 6.
8
Cellular and Molecular Pathways of COVID-19 and Potential Points of Therapeutic Intervention.新型冠状病毒肺炎的细胞和分子途径及潜在治疗干预点
Front Pharmacol. 2020 Jul 29;11:1169. doi: 10.3389/fphar.2020.01169. eCollection 2020.
9
Association of obesity and its genetic predisposition with the risk of severe COVID-19: Analysis of population-based cohort data.肥胖及其遗传易感性与 COVID-19 重症风险的关联:基于人群队列数据的分析。
Metabolism. 2020 Nov;112:154345. doi: 10.1016/j.metabol.2020.154345. Epub 2020 Aug 22.
10
Allergic disorders and susceptibility to and severity of COVID-19: A nationwide cohort study.过敏疾病与 COVID-19 的易感性和严重程度:一项全国性队列研究。
J Allergy Clin Immunol. 2020 Oct;146(4):790-798. doi: 10.1016/j.jaci.2020.08.008. Epub 2020 Aug 15.

正常鼻腔黏膜和慢性鼻窦炎对 SARS-CoV-2 的易感性差异。

Differential susceptibility to SARS-CoV-2 in the normal nasal mucosa and in chronic sinusitis.

机构信息

Department of Otolaryngology, Head and Neck Surgery, Tongji Hospital, School of Medicine, Tongji University, 389 Xincun Road, Putuo District, Shanghai, 200065, P. R. China.

Fundamental Research Center, Department of Neurology and Neurological Rehabilitation, Shanghai Yangzhi Rehabilitation Hospital, School of Medicine, Tongji University, 2209 Guangxing Road, Songjiang District, Shanghai, 200092, P. R. China.

出版信息

Eur J Immunol. 2022 Aug;52(8):1308-1320. doi: 10.1002/eji.202249805. Epub 2022 May 14.

DOI:10.1002/eji.202249805
PMID:35524548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9347577/
Abstract

Human nasal mucosa is susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and serves as a reservoir for viral replication before spreading to other organs (e.g. the lung and brain) and transmission to other individuals. Chronic rhinosinusitis (CRS) is a common respiratory tract disease and there is evidence suggesting that susceptibility to SARS-CoV-2 infection differs between the two known subtypes, eosinophilic CRS and non-ECRS (NECRS). However, the mechanism of SARS-CoV-2 infection in the human nasal mucosa and its association with CRS has not been experimentally validated. In this study, we investigated whether the human nasal mucosa is susceptible to SARS-CoV-2 infection and how different endotypes of CRS impact on viral infection and progression. Primary human nasal mucosa tissue culture revealed highly efficient SARS-CoV-2 viral infection and production, with particularly high susceptibility in the NECRS group. The gene expression differences suggested that human nasal mucosa is highly susceptible to SARS-CoV-2 infection, presumably due to an increase in ACE2-expressing cells and a deficiency in antiviral immune response, especially for NECRS. Importantly, patients with NECRS may be at a particularly high risk of viral infection and transmission, and therefore, close monitoring should be considered.

摘要

人类鼻腔黏膜容易受到严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染,并且在病毒传播到其他器官(例如肺和脑)以及传播给其他个体之前,作为病毒复制的储库。慢性鼻-鼻窦炎(CRS)是一种常见的呼吸道疾病,有证据表明,对 SARS-CoV-2 感染的易感性在两种已知亚型(嗜酸性 CRS 和非嗜酸性 CRS(NECRS))之间有所不同。然而,SARS-CoV-2 在人类鼻腔黏膜中的感染机制及其与 CRS 的关联尚未通过实验验证。在这项研究中,我们研究了人类鼻腔黏膜是否容易受到 SARS-CoV-2 感染,以及不同的 CRS 表型如何影响病毒感染和进展。原代人鼻腔黏膜组织培养显示 SARS-CoV-2 病毒感染和产生非常高效,尤其是在 NECRS 组中具有极高的易感性。基因表达差异表明,人类鼻腔黏膜对 SARS-CoV-2 感染高度敏感,可能是由于 ACE2 表达细胞增加和抗病毒免疫反应缺陷,特别是对于 NECRS。重要的是,NECRS 患者可能面临特别高的病毒感染和传播风险,因此应考虑密切监测。