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Kidney Int. 2020 Jul;98(1):219-227. doi: 10.1016/j.kint.2020.04.003. Epub 2020 Apr 9.
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Likelihood of survival of coronavirus disease 2019.2019冠状病毒病的生存可能性。
Lancet Infect Dis. 2020 Jun;20(6):630-631. doi: 10.1016/S1473-3099(20)30257-7. Epub 2020 Mar 30.
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Targeting the Endocytic Pathway and Autophagy Process as a Novel Therapeutic Strategy in COVID-19.靶向内吞途径和自噬过程作为 COVID-19 的一种新治疗策略。
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Association of Cardiac Injury With Mortality in Hospitalized Patients With COVID-19 in Wuhan, China.新冠肺炎住院患者中心脏损伤与死亡的相关性研究:中国武汉。
JAMA Cardiol. 2020 Jul 1;5(7):802-810. doi: 10.1001/jamacardio.2020.0950.
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Insights from nanomedicine into chloroquine efficacy against COVID-19.纳米医学对氯喹治疗 COVID-19 疗效的启示。
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SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor.严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)进入细胞依赖于 ACE2 和 TMPRSS2,可被一种临床验证的蛋白酶抑制剂所阻断。
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将直接病毒细胞病变假说应用于针对 COVID-19 的药物试验设计。

The application of direct viral cytopathic hypothesis to design drug trials in the battle against COVID-19.

机构信息

Shiraz University of Medical Sciences, Shiraz, Iran.

School of Medicine, University of Central Lancashire, Preston, England.

出版信息

Daru. 2020 Dec;28(2):813-814. doi: 10.1007/s40199-020-00368-3. Epub 2020 Aug 15.

DOI:10.1007/s40199-020-00368-3
PMID:32803688
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7429091/
Abstract

COVID-19 has caused many deaths worldwide. Systemic complications alongside coagulopathy, and ARDS account for the majority of COVID-19 mortalities. The pathogenesis of the disease can be explained by two theories of direct viral cytopathy and systemic inflammatory cascade of events. ACE-2 is shown to be the cellular host receptor for SARS-CoV-2. It might be the key to explain the pathogenesis of systemic complications with a focus on the direct viral cytopathic hypothesis. Different medications tend to show up in many in vitro drug screens. However, more trials are needed to translate their application into in vivo efficacy.

摘要

新型冠状病毒肺炎(COVID-19)在全球范围内造成了许多死亡。合并凝血病和急性呼吸窘迫综合征(ARDS)的全身并发症是 COVID-19 死亡的主要原因。该疾病的发病机制可以用两种理论来解释,即直接病毒细胞病变和全身炎症级联反应。已证实血管紧张素转换酶 2(ACE-2)是 SARS-CoV-2 的细胞宿主受体。它可能是解释全身并发症发病机制的关键,重点是直接病毒细胞病变假说。不同的药物在许多体外药物筛选中都有表现。然而,需要更多的试验将其应用转化为体内疗效。