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本文引用的文献

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Hepatitis B Virus Does Not Interfere With Innate Immune Responses in the Human Liver.乙型肝炎病毒不会干扰人体肝脏中的固有免疫反应。
Gastroenterology. 2018 May;154(6):1778-1790. doi: 10.1053/j.gastro.2018.01.034. Epub 2018 Mar 19.
2
Hepatitis B cure: From discovery to regulatory approval.乙型肝炎治愈:从发现到监管批准。
J Hepatol. 2017 Oct;67(4):847-861. doi: 10.1016/j.jhep.2017.05.008. Epub 2017 Aug 1.
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Hepatitis B virus evades innate immunity of hepatocytes but activates cytokine production by macrophages.乙型肝炎病毒逃避肝细胞的固有免疫,但激活巨噬细胞产生细胞因子。
Hepatology. 2017 Dec;66(6):1779-1793. doi: 10.1002/hep.29348.
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Chinese biopharma starts feeding the global pipeline.中国生物制药企业开始为全球研发线注入力量。
Nat Rev Drug Discov. 2017 Jun 29;16(7):443-446. doi: 10.1038/nrd.2017.94.
5
Interplay between the Hepatitis B Virus and Innate Immunity: From an Understanding to the Development of Therapeutic Concepts.乙型肝炎病毒与固有免疫之间的相互作用:从认识到治疗理念的发展
Viruses. 2017 Apr 28;9(5):95. doi: 10.3390/v9050095.
6
Antiviral Efficacy and Host Immune Response Induction during Sequential Treatment with SB 9200 Followed by Entecavir in Woodchucks.土拨鼠中先使用SB 9200随后使用恩替卡韦进行序贯治疗期间的抗病毒疗效及宿主免疫反应诱导情况
PLoS One. 2017 Jan 5;12(1):e0169631. doi: 10.1371/journal.pone.0169631. eCollection 2017.
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Treatment of chronic hepatitis B infection-2017.慢性乙型肝炎感染的治疗 - 2017 年
Liver Int. 2017 Jan;37 Suppl 1:59-66. doi: 10.1111/liv.13309.
8
Intrahepatic innate immune response pathways are downregulated in untreated chronic hepatitis B.未治疗的慢性乙型肝炎患者肝内固有免疫反应途径下调。
J Hepatol. 2017 May;66(5):897-909. doi: 10.1016/j.jhep.2016.12.024. Epub 2016 Dec 30.
9
Future Therapy for Hepatitis B Virus: Role of Immunomodulators.乙型肝炎病毒的未来治疗:免疫调节剂的作用
Curr Hepatol Rep. 2016;15(4):237-244. doi: 10.1007/s11901-016-0315-9. Epub 2016 Nov 10.
10
HDV RNA replication is associated with HBV repression and interferon-stimulated genes induction in super-infected hepatocytes.丁型肝炎病毒(HDV)RNA复制与重叠感染的肝细胞中乙肝病毒(HBV)抑制及干扰素刺激基因诱导相关。
Antiviral Res. 2016 Dec;136:19-31. doi: 10.1016/j.antiviral.2016.10.006. Epub 2016 Oct 19.

先天免疫调节剂作为慢性乙型肝炎治疗的新型治疗药物。

Modulators of innate immunity as novel therapeutics for treatment of chronic hepatitis B.

机构信息

Department of Biomedicine, University Hospital Basel, University of Basel, Basel CH-4031, Switzerland.

Department of Biomedicine, University Hospital Basel, University of Basel, Basel CH-4031, Switzerland.

出版信息

Curr Opin Virol. 2018 Jun;30:9-17. doi: 10.1016/j.coviro.2018.01.008. Epub 2018 Feb 20.

DOI:10.1016/j.coviro.2018.01.008
PMID:29444493
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5988934/
Abstract

The first line defense mechanisms against viral infection are mediated by the innate immune system. Viral components are detected by infected cells and/or innate immune cells that express different sensory receptors. They in turn mediate induction of direct antiviral mechanisms and further modulation of innate and adaptive immune responses. For evading the innate system, most viruses have evolved efficient mechanisms to block sensing and/or antiviral functions of the innate response. Interestingly, hepatitis B virus (HBV) seems to act like a stealth virus that escapes cell intrinsic antiviral mechanisms through avoiding recognition by the innate system rather than blocking its effector functions. In line with this concept, agonistic activation of innate immunity has emerged as a promising novel anti-HBV therapy approach with several compounds having advanced to the clinical stage.

摘要

第一道防线是固有免疫系统对病毒感染的防御。病毒成分由感染细胞和(或)表达不同感应器的固有免疫细胞检测到。然后,它们转而诱导直接抗病毒机制,并进一步调节固有和适应性免疫反应。为了逃避固有系统,大多数病毒已经进化出有效的机制来阻断固有反应的感应和(或)抗病毒功能。有趣的是,乙型肝炎病毒(HBV)似乎表现得像一种隐形病毒,它通过逃避固有系统的识别而不是阻断其效应功能来逃避细胞内抗病毒机制。与这一概念一致的是,固有免疫的激动剂激活已成为一种很有前途的新型抗乙型肝炎病毒治疗方法,已有几种化合物进入临床阶段。