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Modeling HCV disease in animals: virology, immunology and pathogenesis of HCV and GBV-B infections.在动物中模拟 HCV 疾病:HCV 和 GBV-B 感染的病毒学、免疫学和发病机制。
Front Microbiol. 2014 Dec 8;5:690. doi: 10.3389/fmicb.2014.00690. eCollection 2014.
2
Infection of Common Marmosets with GB Virus B Chimeric Virus Encoding the Major Nonstructural Proteins NS2 to NS4A of Hepatitis C Virus.普通狨猴感染编码丙型肝炎病毒主要非结构蛋白NS2至NS4A的GB病毒B嵌合病毒。
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GB virus B as a model for hepatitis C virus.作为丙型肝炎病毒模型的GB病毒B
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Acute Liver Damage Associated with Innate Immune Activation in a Small Nonhuman Primate Model of Hepacivirus Infection.在一种小型丙型肝炎病毒感染非人灵长类动物模型中,急性肝损伤与天然免疫激活相关。
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Development of a GB virus B marmoset model and its validation with a novel series of hepatitis C virus NS3 protease inhibitors.GB病毒B狨猴模型的建立及其用一系列新型丙型肝炎病毒NS3蛋白酶抑制剂进行的验证。
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GB Virus B and Hepatitis C Virus, Distantly Related Hepaciviruses, Share an Entry Factor, Claudin-1.GB 病毒 B 和丙型肝炎病毒,亲缘关系较远的嗜肝病毒,共用一种进入因子:紧密连接蛋白-1。
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Acute Liver Damage Associated with Innate Immune Activation in a Small Nonhuman Primate Model of Hepacivirus Infection.在一种小型丙型肝炎病毒感染非人灵长类动物模型中,急性肝损伤与天然免疫激活相关。
J Virol. 2016 Sep 29;90(20):9153-62. doi: 10.1128/JVI.01051-16. Print 2016 Oct 15.

本文引用的文献

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Sofosbuvir: a novel oral agent for chronic hepatitis C.索磷布韦:一种用于慢性丙型肝炎的新型口服药物。
Ann Gastroenterol. 2014;27(4):331-337.
2
Clinical course of infection and viral tissue tropism of hepatitis C virus-like nonprimate hepaciviruses in horses.马感染丙型肝炎病毒样非灵长类动物嗜肝病毒的临床过程和病毒组织嗜性。
Hepatology. 2015 Feb;61(2):447-59. doi: 10.1002/hep.27440. Epub 2015 Jan 5.
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Global epidemiology and genotype distribution of the hepatitis C virus infection.全球丙型肝炎病毒感染的流行病学和基因型分布。
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Protective immunity against hepatitis C: many shades of gray.针对丙型肝炎的保护性免疫:诸多灰色地带。
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T-cell immunity and hepatitis C virus reinfection after cure of chronic hepatitis C with an interferon-free antiviral regimen in a chimpanzee.黑猩猩采用无干扰素抗病毒方案治愈慢性丙型肝炎后的T细胞免疫与丙型肝炎病毒再感染
Hepatology. 2014 Nov;60(5):1531-40. doi: 10.1002/hep.27278. Epub 2014 Sep 25.
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Natural history and management of hepatitis C: does sex play a role?丙型肝炎的自然史和治疗:性别是否起作用?
J Infect Dis. 2014 Jul 15;209 Suppl 3:S81-5. doi: 10.1093/infdis/jiu057.
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Why is it so difficult to develop a hepatitis C virus preventive vaccine?为什么开发丙型肝炎病毒预防性疫苗如此困难?
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NS2 proteins of GB virus B and hepatitis C virus share common protease activities and membrane topologies.GB病毒B型和丙型肝炎病毒的NS2蛋白具有共同的蛋白酶活性和膜拓扑结构。
J Virol. 2014 Jul;88(13):7426-44. doi: 10.1128/JVI.00656-14. Epub 2014 Apr 16.
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Therapeutic vaccines against hepatitis C virus.针对丙型肝炎病毒的治疗性疫苗。
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Sofosbuvir: first global approval.索非布韦:全球首个获批
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在动物中模拟 HCV 疾病:HCV 和 GBV-B 感染的病毒学、免疫学和发病机制。

Modeling HCV disease in animals: virology, immunology and pathogenesis of HCV and GBV-B infections.

机构信息

Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center - Harvard Medical School Boston, MA, USA.

出版信息

Front Microbiol. 2014 Dec 8;5:690. doi: 10.3389/fmicb.2014.00690. eCollection 2014.

DOI:10.3389/fmicb.2014.00690
PMID:25538700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4259104/
Abstract

Hepatitis C virus (HCV) infection has become a global public health burden costing billions of dollars in health care annually. Even with rapidly advancing scientific technologies this disease still poses a significant threat due to a lack of vaccines and affordable treatment options. The immune correlates of protection and predisposing factors toward chronicity remain major obstacles to development of HCV vaccines and immunotherapeutics due, at least in part, to lack of a tangible infection animal model. This review discusses the currently available animal models for HCV disease with a primary focus on GB virus B (GBV-B) infection of New World primates that recapitulates the dual Hepacivirus phenotypes of acute viral clearance and chronic pathologic disease. HCV and GBV-B are also closely phylogenetically related and advances in characterization of the immune systems of New World primates have already led to the use of this model for drug testing and vaccine trials. Herein, we discuss the benefits and caveats of the GBV-B infection model and discuss potential avenues for future development of novel vaccines and immunotherapies.

摘要

丙型肝炎病毒 (HCV) 感染已成为全球公共卫生负担,每年在医疗保健方面耗资数十亿美元。尽管科学技术飞速发展,但由于缺乏疫苗和负担得起的治疗方案,这种疾病仍然构成重大威胁。由于缺乏有形的感染动物模型,保护的免疫相关性和慢性发生的诱发因素仍然是 HCV 疫苗和免疫疗法发展的主要障碍。本文讨论了目前用于 HCV 疾病的动物模型,主要集中在新世界灵长类动物的 GB 病毒 B (GBV-B) 感染上,该模型重现了急性病毒清除和慢性病理疾病的双重嗜肝病毒表型。HCV 和 GBV-B 也具有密切的系统发育关系,对新世界灵长类动物免疫系统的特征的研究进展已经导致该模型被用于药物测试和疫苗试验。在此,我们讨论了 GBV-B 感染模型的优缺点,并讨论了开发新型疫苗和免疫疗法的潜在途径。