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丙型肝炎病毒疫苗:挑战与前景

Hepatitis C Virus Vaccine: Challenges and Prospects.

作者信息

Duncan Joshua D, Urbanowicz Richard A, Tarr Alexander W, Ball Jonathan K

机构信息

School of Life Sciences, The University of Nottingham, Nottingham NG7 2UH, UK.

NIHR Nottingham BRC, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham NG7 2UH, UK.

出版信息

Vaccines (Basel). 2020 Feb 17;8(1):90. doi: 10.3390/vaccines8010090.

DOI:10.3390/vaccines8010090
PMID:32079254
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7157504/
Abstract

The hepatitis C virus (HCV) causes both acute and chronic infection and continues to be a global problem despite advances in antiviral therapeutics. Current treatments fail to prevent reinfection and remain expensive, limiting their use to developed countries, and the asymptomatic nature of acute infection can result in individuals not receiving treatment and unknowingly spreading HCV. A prophylactic vaccine is therefore needed to control this virus. Thirty years since the discovery of HCV, there have been major gains in understanding the molecular biology and elucidating the immunological mechanisms that underpin spontaneous viral clearance, aiding rational vaccine design. This review discusses the challenges facing HCV vaccine design and the most recent and promising candidates being investigated.

摘要

丙型肝炎病毒(HCV)可导致急性和慢性感染,尽管抗病毒治疗取得了进展,但它仍然是一个全球性问题。目前的治疗方法无法预防再次感染,而且成本高昂,限制了其在发达国家的使用,急性感染的无症状性质可能导致个体未接受治疗并在不知不觉中传播HCV。因此,需要一种预防性疫苗来控制这种病毒。自HCV发现30年来,在了解分子生物学和阐明支持病毒自发清除的免疫机制方面取得了重大进展,有助于合理设计疫苗。本文综述了HCV疫苗设计面临的挑战以及正在研究的最新且有前景的候选疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c816/7157504/6ef58fad24f2/vaccines-08-00090-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c816/7157504/6ef58fad24f2/vaccines-08-00090-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c816/7157504/6ef58fad24f2/vaccines-08-00090-g001.jpg

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本文引用的文献

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A multiepitope peptide vaccine against HCV stimulates neutralizing humoral and persistent cellular responses in mice.一种针对 HCV 的多表位肽疫苗可刺激小鼠产生中和性体液和持续的细胞应答。
BMC Infect Dis. 2019 Nov 5;19(1):932. doi: 10.1186/s12879-019-4571-5.
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HCV p7 as a novel vaccine-target inducing multifunctional CD4 and CD8 T-cells targeting liver cells expressing the viral antigen.丙型肝炎病毒 p7 作为一种新型疫苗靶点,可诱导针对表达病毒抗原的肝细胞的多功能 CD4 和 CD8 T 细胞。
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Clearance of hepatitis C virus is associated with early and potent but narrowly-directed, Envelope-specific antibodies.
通过糖基工程化中国仓鼠卵巢细胞中的蛋白质-蛋白质相互作用鉴定增强丙型肝炎病毒E1E2亚基候选疫苗的生产
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hsa-miR-548d-3p: a potential microRNA to target nucleocapsid and/or capsid genes in multiple members of the Flaviviridae family.hsa-miR-548d-3p:一种靶向黄病毒科多个成员核衣壳和/或衣壳基因的潜在微小RNA。
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Development of Virus-Like Particles (VLPs) for Hepatitis C Virus genotype 4: a novel approach for vaccine development in Egypt.丙型肝炎病毒4型病毒样颗粒(VLPs)的研发:埃及疫苗研发的新方法
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Acute Hepatitis C: Current Status and Future Perspectives.急性丙型肝炎:现状与未来展望
Viruses. 2024 Nov 6;16(11):1739. doi: 10.3390/v16111739.
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Viral etiologies of acute liver failure.急性肝衰竭的病毒病因
World J Virol. 2024 Sep 25;13(3):97973. doi: 10.5501/wjv.v13.i3.97973.
8
The hepatitis C virus envelope protein complex is a dimer of heterodimers.丙型肝炎病毒包膜蛋白复合物是异二聚体的二聚体。
Nature. 2024 Sep;633(8030):704-709. doi: 10.1038/s41586-024-07783-5. Epub 2024 Sep 4.
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An Increase in the Prevalence of Clinically Relevant Resistance-Associated Substitutions in Four Direct-Acting Antiviral Regimens: A Study Using GenBank HCV Sequences.四种直接作用抗病毒方案中临床相关耐药相关替代位点流行率的增加:一项使用GenBank HCV序列的研究
Pathogens. 2024 Aug 9;13(8):674. doi: 10.3390/pathogens13080674.
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Epidemiologic and clinical updates on viral infections in Saudi Arabia.沙特阿拉伯病毒感染的流行病学与临床最新情况
Saudi Pharm J. 2024 Jul;32(7):102126. doi: 10.1016/j.jsps.2024.102126. Epub 2024 Jun 8.
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Sci Rep. 2019 Sep 16;9(1):13300. doi: 10.1038/s41598-019-49454-w.
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Direct-Acting Antiviral Treatment of HCV Infection Does Not Resolve the Dysfunction of Circulating CD8 T-Cells in Advanced Liver Disease.直接作用抗病毒药物治疗 HCV 感染并不能改善晚期肝病患者循环 CD8+T 细胞的功能障碍。
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