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本文引用的文献

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Oral Sabizabulin for High-Risk, Hospitalized Adults with Covid-19: Interim Analysis.口服沙比沙布林治疗 COVID-19 高危住院成人:中期分析。
NEJM Evid. 2022 Sep;1(9):EVIDoa2200145. doi: 10.1056/EVIDoa2200145. Epub 2022 Jul 6.
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Assessing the effect of selective serotonin reuptake inhibitors in the prevention of post-acute sequelae of COVID-19.评估选择性5-羟色胺再摄取抑制剂在预防新型冠状病毒肺炎急性后遗症中的作用。
Comput Struct Biotechnol J. 2024 Jan 9;24:115-125. doi: 10.1016/j.csbj.2023.12.045. eCollection 2024 Dec.
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Outpatient treatment of COVID-19 and incidence of post-COVID-19 condition over 10 months (COVID-OUT): a multicentre, randomised, quadruple-blind, parallel-group, phase 3 trial.COVID-19 门诊治疗和 COVID-19 后状况的发生率超过 10 个月(COVID-OUT):一项多中心、随机、四盲、平行组、3 期试验。
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Relationship between antidepressants and severity of SARS-CoV-2 Omicron infection: a retrospective cohort study using real-world data.抗抑郁药与新型冠状病毒奥密克戎变异株感染严重程度之间的关系:一项使用真实世界数据的回顾性队列研究
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Oral Fluvoxamine With Inhaled Budesonide for Treatment of Early-Onset COVID-19 : A Randomized Platform Trial.口服氟伏沙明联合布地奈德治疗早期 COVID-19:一项随机平台试验。
Ann Intern Med. 2023 May;176(5):667-675. doi: 10.7326/M22-3305. Epub 2023 Apr 18.
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Early Treatment with Pegylated Interferon Lambda for Covid-19.聚乙二醇干扰素 λ 早期治疗 COVID-19。
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Efficacy and safety of early soluble urokinase plasminogen receptor plasma-guided anakinra treatment of COVID-19 pneumonia: A subgroup analysis of the SAVE-MORE randomised trial.早期可溶性尿激酶型纤溶酶原受体血浆引导下阿那白滞素治疗新冠肺炎肺炎的疗效和安全性:SAVE-MORE随机试验的亚组分析
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The WHO estimates of excess mortality associated with the COVID-19 pandemic.世界卫生组织对 COVID-19 大流行相关超额死亡人数的估计。
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Enhanced neutralization resistance of SARS-CoV-2 Omicron subvariants BQ.1, BQ.1.1, BA.4.6, BF.7, and BA.2.75.2.奥密克戎变异株 BQ.1、BQ.1.1、BA.4.6、BF.7 和 BA.2.75.2 增强型中和抗性。
Cell Host Microbe. 2023 Jan 11;31(1):9-17.e3. doi: 10.1016/j.chom.2022.11.012. Epub 2022 Nov 22.
10
Metformin suppresses SARS-CoV-2 in cell culture.二甲双胍在细胞培养中可抑制新型冠状病毒。
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经临床评估的对生物战剂具有治疗潜力的新冠病毒疾病药物。

Clinically Evaluated COVID-19 Drugs with Therapeutic Potential for Biological Warfare Agents.

作者信息

Dechtman Ido-David, Ankory Ran, Sokolinsky Keren, Krasner Esther, Weiss Libby, Gal Yoav

机构信息

Pulmonology Department, Edith Wolfson Medical Center, 62 Halochamim Street, Holon 5822012, Israel.

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.

出版信息

Microorganisms. 2023 Jun 14;11(6):1577. doi: 10.3390/microorganisms11061577.

DOI:10.3390/microorganisms11061577
PMID:37375079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10304720/
Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) outbreak resulted in hundreds of millions of coronavirus cases, as well as millions of deaths worldwide. Coronavirus Disease 2019 (COVID-19), the disease resulting from exposure to this pathogen, is characterized, among other features, by a pulmonary pathology, which can progress to "cytokine storm", acute respiratory distress syndrome (ARDS), respiratory failure and death. Vaccines are the unsurpassed strategy for prevention and protection against the SARS-CoV-2 infection. However, there is still an extremely high number of severely ill people from at-risk populations. This may be attributed to waning immune response, variant-induced breakthrough infections, unvaccinated population, etc. It is therefore of high importance to utilize pharmacological-based treatments, despite the progression of the global vaccination campaign. Until the approval of Paxlovid, an efficient and highly selective anti-SARS-CoV-2 drug, and the broad-spectrum antiviral agent Lagevrio, many pharmacological-based countermeasures were, and still are, being evaluated in clinical trials. Some of these are host-directed therapies (HDTs), which modulate the endogenic response against the virus, and therefore may confer efficient protection against a wide array of pathogens. These could potentially include Biological Warfare Agents (BWAs), exposure to which may lead to mass casualties due to disease severity and a possible lack of efficient treatment. In this review, we assessed the recent literature on drugs under advanced clinical evaluation for COVID-19 with broad spectrum activity, including antiviral agents and HDTs, which may be relevant for future coping with BWAs, as well as with other agents, in particular respiratory infections.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的爆发导致全球数亿人感染冠状病毒,并造成数百万人死亡。2019冠状病毒病(COVID-19)是由接触这种病原体引起的疾病,其特征之一是肺部病变,可发展为“细胞因子风暴”、急性呼吸窘迫综合征(ARDS)、呼吸衰竭和死亡。疫苗是预防和抵御SARS-CoV-2感染的无与伦比的策略。然而,高危人群中仍有大量重症患者。这可能归因于免疫反应减弱、变异毒株导致的突破性感染、未接种疫苗的人群等。因此,尽管全球疫苗接种运动在推进,但利用基于药理学的治疗方法仍然非常重要。在高效且高度选择性的抗SARS-CoV-2药物帕罗韦德(Paxlovid)和广谱抗病毒药物 Lagevrio获批之前,许多基于药理学的应对措施过去一直在、现在也仍在临床试验中进行评估。其中一些是宿主导向疗法(HDTs),它调节针对病毒的内源性反应,因此可能对多种病原体提供有效的保护。这些病原体可能包括生物战剂(BWAs),接触生物战剂可能因疾病严重程度和可能缺乏有效治疗而导致大量人员伤亡。在本综述中,我们评估了近期有关正在进行临床高级评估的具有广谱活性的COVID-19药物的文献,包括抗病毒药物和宿主导向疗法,这些药物可能与未来应对生物战剂以及其他病原体,特别是呼吸道感染有关。