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探索激酶抑制剂作为治疗人类沙粒病毒感染的方法。

Exploring kinase inhibitors as therapies for human arenavirus infections.

作者信息

Vela Eric M, Bowick Gavin C, Herzog Norbert K, Aronson Judith F

机构信息

Battelle Biomedical Research Center (BBRC), 505 King Avenue, JM8-1-096, Columbus, OH 43201-2693, USA Tel.: +1 614 424 7998; ;

出版信息

Future Virol. 2008;3(3):243-251. doi: 10.2217/17460794.3.3.243.

DOI:10.2217/17460794.3.3.243
PMID:22211137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3246634/
Abstract

Arenaviruses are rodent-borne RNA viruses, and some have the capacity to cause hemorrhagic fever and death in infected individuals and thus have been identified as a potential bioterrorism threat. Ribavirin and supportive care are currently the approved therapeutic options for individuals suffering from arenavirus-induced hemorrhagic fever. However, new research has suggested that immune plasma treatment or kinase inhibitors may provide a therapeutic option for treating arenavirus infections in humans. This article puts forth a perspective as to the potential use of kinase inhibitors as an antiviral therapeutic for arenavirus infections.

摘要

沙粒病毒是由啮齿动物传播的RNA病毒,其中一些能够在受感染个体中引发出血热并导致死亡,因此被认定为潜在的生物恐怖主义威胁。利巴韦林和支持性护理是目前获批用于治疗沙粒病毒引起的出血热患者的治疗选择。然而,新的研究表明,免疫血浆治疗或激酶抑制剂可能为治疗人类沙粒病毒感染提供一种治疗选择。本文就激酶抑制剂作为沙粒病毒感染的抗病毒治疗方法的潜在用途提出了一种观点。

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Exploring kinase inhibitors as therapies for human arenavirus infections.探索激酶抑制剂作为治疗人类沙粒病毒感染的方法。
Future Virol. 2008;3(3):243-251. doi: 10.2217/17460794.3.3.243.
2
Animal models, prophylaxis, and therapeutics for arenavirus infections.动物模型、预防和治疗沙粒病毒感染。
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引用本文的文献

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Animal models, prophylaxis, and therapeutics for arenavirus infections.动物模型、预防和治疗沙粒病毒感染。
Viruses. 2012 Sep;4(9):1802-29. doi: 10.3390/v4091802. Epub 2012 Sep 24.
2
Host cell factors as antiviral targets in arenavirus infection.宿主细胞因子作为沙粒病毒感染的抗病毒靶点。
Viruses. 2012 Sep;4(9):1569-91. doi: 10.3390/v4091569. Epub 2012 Sep 13.
3
Progress in the experimental therapy of severe arenaviral infections.严重沙粒病毒感染的实验治疗进展。
Future Microbiol. 2011 Dec;6(12):1429-41. doi: 10.2217/fmb.11.132.
4
Meta-analysis of high-throughput datasets reveals cellular responses following hemorrhagic fever virus infection.高通量数据集的荟萃分析揭示了出血热病毒感染后的细胞反应。
Viruses. 2011 May;3(5):613-9. doi: 10.3390/v3050613. Epub 2011 May 12.
5
Proteomic analysis of Pichindé virus infection identifies differential expression of prothymosin-alpha.皮钦德病毒感染的蛋白质组学分析确定了胸腺素α原的差异表达。
J Biomed Biotechnol. 2010;2010. doi: 10.1155/2010/956823. Epub 2010 Apr 18.
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Comparative pathogenesis and systems biology for biodefense virus vaccine development.用于生物防御病毒疫苗开发的比较发病机制与系统生物学
J Biomed Biotechnol. 2010;2010:236528. doi: 10.1155/2010/236528. Epub 2010 Jun 6.
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Attenuated and lethal variants of Pichindé virus induce differential patterns of NF-kappaB activation suggesting a potential target for novel therapeutics.皮钦德病毒的减毒和致死变体诱导不同的 NF-κB 激活模式,提示了一种新型治疗药物的潜在靶点。
Viral Immunol. 2009 Dec;22(6):457-62. doi: 10.1089/vim.2009.0034.

本文引用的文献

1
Protein kinase inhibitors of the quinazoline class exert anti-cytomegaloviral activity in vitro and in vivo.喹唑啉类蛋白激酶抑制剂在体外和体内均具有抗巨细胞病毒活性。
Antiviral Res. 2008 Jul;79(1):49-61. doi: 10.1016/j.antiviral.2008.01.154. Epub 2008 Feb 22.
2
In vivo activity of ABT-869, a multi-target kinase inhibitor, against acute myeloid leukemia with wild-type FLT3 receptor.多靶点激酶抑制剂ABT-869对具有野生型FLT3受体的急性髓系白血病的体内活性
Leuk Res. 2008 Jul;32(7):1091-100. doi: 10.1016/j.leukres.2007.11.025. Epub 2007 Dec 26.
3
Treatment of Argentine hemorrhagic fever.阿根廷出血热的治疗
Antiviral Res. 2008 Apr;78(1):132-9. doi: 10.1016/j.antiviral.2007.10.010. Epub 2007 Nov 20.
4
Intracellular bacterial growth is controlled by a kinase network around PKB/AKT1.细胞内细菌生长受围绕蛋白激酶B/蛋白激酶B1(PKB/AKT1)的激酶网络控制。
Nature. 2007 Nov 29;450(7170):725-30. doi: 10.1038/nature06345.
5
Genistein treatment of cells inhibits arenavirus infection.金雀异黄素对细胞的处理可抑制沙粒病毒感染。
Antiviral Res. 2008 Feb;77(2):153-6. doi: 10.1016/j.antiviral.2007.09.005. Epub 2007 Oct 8.
6
Arenavirus entry occurs through a cholesterol-dependent, non-caveolar, clathrin-mediated endocytic mechanism.沙粒病毒通过胆固醇依赖性、非小窝、网格蛋白介导的内吞机制进入细胞。
Virology. 2007 Dec 5;369(1):1-11. doi: 10.1016/j.virol.2007.07.014. Epub 2007 Aug 14.
7
In vitro and in vivo activities of T-705 against arenavirus and bunyavirus infections.T-705 对沙粒病毒和布尼亚病毒感染的体外及体内活性
Antimicrob Agents Chemother. 2007 Sep;51(9):3168-76. doi: 10.1128/AAC.00356-07. Epub 2007 Jul 2.
8
Characterization of Junin arenavirus cell entry.胡宁沙粒病毒细胞进入的特征描述。
J Gen Virol. 2007 Jun;88(Pt 6):1776-1784. doi: 10.1099/vir.0.82808-0.
9
A ML29 reassortant virus protects guinea pigs against a distantly related Nigerian strain of Lassa virus and can provide sterilizing immunity.一种ML29重配病毒可保护豚鼠抵御远缘相关的尼日利亚拉沙病毒株,并能提供无菌免疫。
Vaccine. 2007 May 16;25(20):4093-102. doi: 10.1016/j.vaccine.2007.02.038. Epub 2007 Feb 27.
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Thioaptamer decoy targeting of AP-1 proteins influences cytokine expression and the outcome of arenavirus infections.靶向 AP-1 蛋白的硫适配体诱饵影响细胞因子表达和沙粒病毒感染的结果。
J Gen Virol. 2007 Mar;88(Pt 3):981-990. doi: 10.1099/vir.0.82499-0.