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1
Remdesivir plus standard of care versus standard of care alone for the treatment of patients admitted to hospital with COVID-19 (DisCoVeRy): a phase 3, randomised, controlled, open-label trial.瑞德西韦联合标准治疗与单纯标准治疗用于治疗因 COVID-19 住院的患者(DisCoVeRy):一项 3 期、随机、对照、开放标签试验。
Lancet Infect Dis. 2022 Feb;22(2):209-221. doi: 10.1016/S1473-3099(21)00485-0. Epub 2021 Sep 14.
2
Interleukin-1RA Mitigates SARS-CoV-2-Induced Inflammatory Lung Vascular Leakage and Mortality in Humanized K18-hACE-2 Mice.白细胞介素-1RA 减轻人源化 K18-hACE-2 小鼠中 SARS-CoV-2 诱导的炎症性肺血管渗漏和死亡率。
Arterioscler Thromb Vasc Biol. 2021 Nov;41(11):2773-2785. doi: 10.1161/ATVBAHA.121.316925. Epub 2021 Sep 9.
3
COVID-19 generates hyaluronan fragments that directly induce endothelial barrier dysfunction.COVID-19 产生透明质酸片段,直接诱导内皮屏障功能障碍。
JCI Insight. 2021 Sep 8;6(17):e147472. doi: 10.1172/jci.insight.147472.
4
Bamlanivimab plus Etesevimab in Mild or Moderate Covid-19.巴尼韦单抗/依特司韦单抗在轻中度 COVID-19 中的应用。
N Engl J Med. 2021 Oct 7;385(15):1382-1392. doi: 10.1056/NEJMoa2102685. Epub 2021 Jul 14.
5
A robust SARS-CoV-2 replication model in primary human epithelial cells at the air liquid interface to assess antiviral agents.在气液界面的原代人上皮细胞中建立稳健的 SARS-CoV-2 复制模型,以评估抗病毒药物。
Antiviral Res. 2021 Aug;192:105122. doi: 10.1016/j.antiviral.2021.105122. Epub 2021 Jun 26.
6
Tofacitinib in Patients Hospitalized with Covid-19 Pneumonia.托法替布治疗因 COVID-19 肺炎住院的患者。
N Engl J Med. 2021 Jul 29;385(5):406-415. doi: 10.1056/NEJMoa2101643. Epub 2021 Jun 16.
7
Mitofusin-2 stabilizes adherens junctions and suppresses endothelial inflammation via modulation of β-catenin signaling.线粒体融合蛋白 2 通过调节β-连环蛋白信号稳定黏着连接,并抑制血管内皮炎症。
Nat Commun. 2021 May 12;12(1):2736. doi: 10.1038/s41467-021-23047-6.
8
Neutralizing monoclonal antibodies for treatment of COVID-19.用于治疗 COVID-19 的中和单克隆抗体。
Nat Rev Immunol. 2021 Jun;21(6):382-393. doi: 10.1038/s41577-021-00542-x. Epub 2021 Apr 19.
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Orally delivered MK-4482 inhibits SARS-CoV-2 replication in the Syrian hamster model.口服给药的MK-4482在叙利亚仓鼠模型中抑制新冠病毒复制。
Nat Commun. 2021 Apr 16;12(1):2295. doi: 10.1038/s41467-021-22580-8.
10
An Immuno-Cardiac Model for Macrophage-Mediated Inflammation in COVID-19 Hearts.一种用于新冠肺炎心脏中巨噬细胞介导炎症的免疫心脏模型。
Circ Res. 2021 Jun 25;129(1):33-46. doi: 10.1161/CIRCRESAHA.121.319060. Epub 2021 Apr 15.

新型冠状病毒感染所致肺损伤的机制。

Mechanisms of Lung Injury Induced by SARS-CoV-2 Infection.

机构信息

Department of Surgery, Weill Cornell Medicine, New York, New York.

Division of Cardiology, Department of Medicine, University of Illinois College of Medicine, Chicago, Illinois.

出版信息

Physiology (Bethesda). 2022 Mar 1;37(2):88-100. doi: 10.1152/physiol.00033.2021. Epub 2021 Oct 26.

DOI:10.1152/physiol.00033.2021
PMID:34698589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8873036/
Abstract

The lung is the major target organ of SARS-CoV-2 infection, which causes COVID-19. Here, we outline the multistep mechanisms of lung epithelial and endothelial injury induced by SARS-CoV-2: direct viral infection, chemokine/cytokine-mediated damage, and immune cell-mediated lung injury. Finally, we discuss the recent progress in terms of antiviral therapeutics as well as the development of anti-inflammatory or immunomodulatory therapeutic approaches. This review also provides a systematic overview of the models for studying SARS-CoV-2 infection and discusses how an understanding of mechanisms of lung injury will help identify potential targets for future drug development to mitigate lung injury.

摘要

肺是 SARS-CoV-2 感染的主要靶器官,可引起 COVID-19。在这里,我们概述了 SARS-CoV-2 引起的肺上皮细胞和内皮细胞损伤的多步骤机制:直接病毒感染、趋化因子/细胞因子介导的损伤和免疫细胞介导的肺损伤。最后,我们讨论了抗病毒治疗以及抗炎或免疫调节治疗方法的最新进展。本综述还系统地概述了研究 SARS-CoV-2 感染的模型,并讨论了对肺损伤机制的理解如何有助于确定未来药物开发的潜在靶点,以减轻肺损伤。