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本文引用的文献

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Longitudinal profiles of immunoglobulin G antibodies against severe acute respiratory syndrome coronavirus components and neutralizing activities in recovered patients.康复患者中针对严重急性呼吸综合征冠状病毒成分的免疫球蛋白G抗体纵向分布及中和活性
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Evidence that TMPRSS2 activates the severe acute respiratory syndrome coronavirus spike protein for membrane fusion and reduces viral control by the humoral immune response.证据表明 TMPRSS2 激活严重急性呼吸综合征冠状病毒刺突蛋白进行膜融合,并降低体液免疫应答对病毒的控制。
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Single-dose intranasal administration with mDEF201 (adenovirus vectored mouse interferon-alpha) confers protection from mortality in a lethal SARS-CoV BALB/c mouse model.单次鼻腔内给予 mDEF201(腺病毒载体鼠干扰素-α)可预防致死性 SARS-CoV BALB/c 小鼠模型的死亡。
Antiviral Res. 2011 Jan;89(1):75-82. doi: 10.1016/j.antiviral.2010.11.007. Epub 2010 Nov 18.
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Zn(2+) inhibits coronavirus and arterivirus RNA polymerase activity in vitro and zinc ionophores block the replication of these viruses in cell culture.锌(2+)在体外抑制冠状病毒和动脉病毒 RNA 聚合酶的活性,而锌离子载体则阻断这些病毒在细胞培养中的复制。
PLoS Pathog. 2010 Nov 4;6(11):e1001176. doi: 10.1371/journal.ppat.1001176.
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Genomic characterization of severe acute respiratory syndrome-related coronavirus in European bats and classification of coronaviruses based on partial RNA-dependent RNA polymerase gene sequences.严重急性呼吸系统综合征相关冠状病毒的基因组特征在欧洲蝙蝠和分类冠状病毒基于部分 RNA 依赖的 RNA 聚合酶基因序列。
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Severe acute respiratory syndrome and coronavirus.严重急性呼吸系统综合征与冠状病毒。
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Severe acute respiratory syndrome coronavirus papain-like novel protease inhibitors: design, synthesis, protein-ligand X-ray structure and biological evaluation.严重急性呼吸系统综合症冠状病毒木瓜蛋白酶样新型蛋白酶抑制剂:设计、合成、蛋白-配体 X 射线结构和生物学评估。
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Induction of interferon-gamma-inducible protein 10 by SARS-CoV infection, interferon alfacon 1 and interferon inducer in human bronchial epithelial Calu-3 cells and BALB/c mice.严重急性呼吸综合征冠状病毒(SARS-CoV)感染、干扰素 alfacon 1 和干扰素诱导剂在人支气管上皮 Calu-3 细胞及 BALB/c 小鼠中对干扰素γ诱导蛋白 10 的诱导作用
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Severe acute respiratory syndrome (SARS).严重急性呼吸综合征(SARS)。
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抗严重急性呼吸综合征冠状病毒化疗的最新进展。

Recent developments in anti-severe acute respiratory syndrome coronavirus chemotherapy.

作者信息

Barnard Dale L, Kumaki Yohichi

机构信息

Utah State University, Institute for Antiviral Research, Department of Animal, Dairy & Veterinary Science, 5600 Old Main Hill, Logan, UT 84322, USA.

出版信息

Future Virol. 2011 May;6(5):615-631. doi: 10.2217/fvl.11.33.

DOI:10.2217/fvl.11.33
PMID:21765859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3136164/
Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV) emerged in early 2003 to cause a very severe acute respiratory syndrome, which eventually resulted in a 10% case-fatality rate. Owing to excellent public health measures that isolated focus cases and their contacts, and the use of supportive therapies, the epidemic was suppressed to the point that further cases have not appeared since 2005. However, despite intensive research since then (over 3500 publications), it remains an untreatable disease. The potential for re-emergence of the SARS-CoV or a similar virus with unknown but potentially serious consequences remains high. This is due in part to the extreme genetic variability of RNA viruses such as the coronaviruses, the many animal reservoirs that seem to be able host the SARS-CoV in which reassortment or recombination events could occur and the ability coronaviruses have to transmit relatively rapidly from species to species in a short period of time. Thus, it seems prudent to continue to explore and develop antiviral chemotherapies to treat SARS-CoV infections. To this end, the various efficacious anti-SARS-CoV therapies recently published from 2007 to 2010 are reviewed in this article. In addition, compounds that have been tested in various animal models and were found to reduce virus lung titers and/or were protective against death in lethal models of disease, or otherwise have been shown to ameliorate the effects of viral infection, are also reported.

摘要

严重急性呼吸综合征冠状病毒(SARS-CoV)于2003年初出现,引发了一种极为严重的急性呼吸综合征,最终导致10%的病死率。由于采取了出色的公共卫生措施,隔离了聚集性病例及其接触者,并采用了支持性疗法,疫情得到了控制,自2005年以来未再出现新的病例。然而,尽管从那时起进行了深入研究(超过3500篇出版物),但它仍然是一种无法治疗的疾病。SARS-CoV或类似病毒再次出现并带来未知但可能严重后果的可能性仍然很高。这部分是由于RNA病毒(如冠状病毒)具有极高的基因变异性、许多似乎能够宿主SARS-CoV的动物宿主,在这些宿主中可能发生重配或重组事件,以及冠状病毒能够在短时间内相对快速地在物种间传播。因此,继续探索和开发抗病毒化疗药物来治疗SARS-CoV感染似乎是谨慎之举。为此,本文对2007年至2010年期间最近发表的各种有效的抗SARS-CoV疗法进行了综述。此外,还报告了在各种动物模型中进行过测试、被发现可降低病毒肺滴度和/或在致死性疾病模型中具有保护作用以免于死亡、或以其他方式显示可改善病毒感染影响的化合物。