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Immune-modulators to combat hepatitis B virus infection: From IFN-alpha to novel investigational immunotherapeutic strategies

机译:抵抗乙型肝炎病毒感染的免疫调节剂:从IFN-α到新颖的研究性免疫治疗策略

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摘要

Chronic hepatitis B virus (HBV) infection remains a major challenge for clinicians, as there are only two types of approved therapies: interferon-alpha (IFN-alpha) or its pegylated form, Peg-IFN-alpha and nucleoside analogs (e.g. tenofovir, entecavir...). The first are used as finite-duration treatments of around 48-52 weeks, while the second must be taken life-long to prevent rebound. Other immune-modulators, including other types of recombinant IFNs and cytokines/chemokines, could be developed for treating chronic hepatitis B. Alternatively, strategies aimed either at restoring or favoring the endogenous production of IFNs, cytokines and/or chemokines, or at alleviating HBV-mediated inhibitory processes could also be envisaged. In this article, we review current investigational, preclinical and clinical efforts to implement immune-modulatory components in the therapy of chronic hepatitis B. This review forms part of a symposium in Antiviral Research on "An unfinished story: from the discovery of the Australia antigen to the development of new curative therapies for hepatitis B". (C) 2015 Elsevier B.V. All rights reserved.
机译:慢性乙型肝炎病毒(HBV)感染仍然是临床医生面临的主要挑战,因为批准的疗法只有两种:干扰素-α(IFN-alpha)或其聚乙二醇化形式,Peg-IFN-α和核苷类似物(例如替诺福韦,恩替卡韦...)。第一种用作约48-52周的有限持续时间治疗,而第二种必须终身服用以防止反弹。可以开发其他免疫调节剂,包括其他类型的重组IFN和细胞因子/趋化因子,以治疗慢性乙型肝炎。或者,旨在恢复或促进内源性生产IFN,细胞因子和/或趋化因子或减轻HBV的策略还可以设想介导的抑制过程。在本文中,我们回顾了目前在慢性乙型肝炎的治疗中实施免疫调节成分的研究,临床前和临床工作。该综述构成了“未完成的故事:来自澳大利亚抗原的发现”抗病毒研究研讨会的一部分。开发新的乙型肝炎治疗药物”。 (C)2015 Elsevier B.V.保留所有权利。

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