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Crimean-Congo hemorrhagic fever.克里米亚-刚果出血热
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The host inflammatory response contributes to disease severity in Crimean-Congo hemorrhagic fever virus infected mice.宿主炎症反应导致克里米亚-刚果出血热病毒感染的小鼠疾病严重程度增加。
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本文引用的文献

1
A DNA vaccine for Crimean-Congo hemorrhagic fever protects against disease and death in two lethal mouse models.一种用于克里米亚-刚果出血热的DNA疫苗在两种致死性小鼠模型中可预防疾病和死亡。
PLoS Negl Trop Dis. 2017 Sep 18;11(9):e0005908. doi: 10.1371/journal.pntd.0005908. eCollection 2017 Sep.
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Infection prevention and control practice for Crimean-Congo hemorrhagic fever-A multi-center cross-sectional survey in Eurasia.克里米亚-刚果出血热的感染预防与控制实践——一项在欧亚大陆开展的多中心横断面调查
PLoS One. 2017 Sep 8;12(9):e0182315. doi: 10.1371/journal.pone.0182315. eCollection 2017.
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Development of vaccines against Crimean-Congo haemorrhagic fever virus.抗克里米亚-刚果出血热病毒疫苗的研发
Vaccine. 2017 Oct 20;35(44):6015-6023. doi: 10.1016/j.vaccine.2017.05.031. Epub 2017 Jul 4.
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Cytokine response in crimean-congo hemorrhagic fever virus infection.克里米亚-刚果出血热病毒感染中的细胞因子反应。
J Med Virol. 2017 Oct;89(10):1707-1713. doi: 10.1002/jmv.24864. Epub 2017 Jul 6.
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Crimean-Congo Hemorrhagic Fever in Humanized Mice Reveals Glial Cells as Primary Targets of Neurological Infection.人源化小鼠的克里米亚-刚果出血热揭示神经胶质细胞是神经感染的主要靶点。
J Infect Dis. 2017 Dec 12;216(11):1386-1397. doi: 10.1093/infdis/jix215.
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Experimental Treatment of Ebola Virus Disease with Brincidofovir.用布林西多福韦对埃博拉病毒病进行实验性治疗。
PLoS One. 2016 Sep 9;11(9):e0162199. doi: 10.1371/journal.pone.0162199. eCollection 2016.
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Prognostic factors, pathophysiology and novel biomarkers in Crimean-Congo hemorrhagic fever.克里米亚-刚果出血热的预后因素、病理生理学及新型生物标志物
Antiviral Res. 2016 Aug;132:233-43. doi: 10.1016/j.antiviral.2016.06.011. Epub 2016 Jul 1.
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Protective effects of a Modified Vaccinia Ankara-based vaccine candidate against Crimean-Congo Haemorrhagic Fever virus require both cellular and humoral responses.一种基于改良安卡拉痘苗病毒的候选疫苗对克里米亚-刚果出血热病毒的保护作用需要细胞免疫和体液免疫反应。
PLoS One. 2016 Jun 7;11(6):e0156637. doi: 10.1371/journal.pone.0156637. eCollection 2016.
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Progression of Ebola Therapeutics During the 2014-2015 Outbreak.2014-2015 年埃博拉疫情期间的治疗方法进展。
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The Synthetic Antiviral Drug Arbidol Inhibits Globally Prevalent Pathogenic Viruses.合成抗病毒药物阿比多尔可抑制全球流行的致病性病毒。
J Virol. 2016 Jan 6;90(6):3086-92. doi: 10.1128/JVI.02077-15.

克里米亚-刚果出血热病毒:动物模型及医学应对措施的过去、现状与未来展望

Crimean-Congo haemorrhagic fever virus: Past, present and future insights for animal modelling and medical countermeasures.

作者信息

Mendoza E J, Warner B, Safronetz D, Ranadheera C

机构信息

Zoonotic Diseases and Special Pathogens, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.

Department of Medical Microbiology, University of Manitoba, Winnipeg, MB, Canada.

出版信息

Zoonoses Public Health. 2018 Aug;65(5):465-480. doi: 10.1111/zph.12469. Epub 2018 Apr 20.

DOI:10.1111/zph.12469
PMID:29676526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7165601/
Abstract

Crimean-Congo haemorrhagic fever (CCHF) is a widespread tick-borne viral zoonosis with a case-fatality rate ranging from 9% to 50% in humans. Although a licensed vaccine to prevent infection by the CCHF virus (CCHFV) exists, its ability to induce neutralizing antibodies is limited and its efficacy against CCHFV remains undetermined. In addition, controlling CCHF infections by eradication of the tick reservoir has been ineffective, both economically and logistically, and the treatment options for CCHF remain limited. In this review, we first critically discuss the existing animal models to evaluate therapeutics for CCHF. We then review the therapeutic options for CCHF that have been investigated in human cases, followed by investigational drugs that have been evaluated in pre-clinical studies. We highlight the importance of understanding human prognostic factors in developing an animal model for CCHF that recapitulates hallmarks of human disease and its implication for selecting therapeutic candidates.

摘要

克里米亚-刚果出血热(CCHF)是一种广泛传播的蜱传病毒性人畜共患病,人类病死率在9%至50%之间。尽管有一种预防克里米亚-刚果出血热病毒(CCHFV)感染的许可疫苗,但它诱导中和抗体的能力有限,其对CCHFV的疗效仍未确定。此外,通过消灭蜱虫宿主来控制CCHF感染在经济和后勤方面都没有效果,CCHF的治疗选择仍然有限。在本综述中,我们首先批判性地讨论现有的用于评估CCHF治疗方法的动物模型。然后我们回顾了在人类病例中研究过的CCHF治疗选择,接着是在临床前研究中评估过的研究性药物。我们强调了在开发一种概括人类疾病特征的CCHF动物模型时理解人类预后因素的重要性及其对选择治疗候选药物的意义。