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Chronic hepatitis B: Virology, natural history, current management and a glimpse at future opportunities

机译:慢性乙型肝炎:病毒学,自然病史,目前的管理方法以及对未来机会的了解

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摘要

The host immune system plays an important role in chronic hepatitis B (CHB), both in viral clearance and hepatocellular damage. Advances in our understanding of the natural history of the disease have led to redefining the major phases of infection, with the "high replicative, low inflammatory" phase now replacing what was formerly termed the "immune tolerant" phase, and the "nonreplicative phase" replacing what was formerly termed the "inactive carrier" phase. As opposed to the earlier view that HBV establishes chronic infection by exploiting the immaturity of the neonate's immune system, new findings on trained immunity show that the host is already somewhat "matured" following birth, and is actually very capable of responding immunologically, potentially altering future hepatitis B treatment strategies. While existing therapies are effective in reducing viral load and necroinflammation, often restoring the patient to near-normal health, they do not lead to a cure except in very rare cases and, in many patients, viremia rebounds after cessation of treatment. Researchers are now challenged to devise therapies that will eliminate infection, with a particular focus on eliminating the persistence of viral cccDNA in the nuclei of hepatocytes. In the context of chronic hepatitis B, new definitions of 'cure' are emerging, such as 'functional' and 'virological' cure, defined by stable off-therapy suppression of viremia and antigenemia, and the normalization of serum ALT and other liver-related laboratory tests. Continued advances in the understanding of the complex biology of chronic hepatitis B have resulted in the development of new, experimental therapies targeting viral and host factors and pathways previously not accessible to therapy, approaches which may lead to virological cures in the near term and functional cures upon long term follow-up. This article 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:宿主免疫系统在慢性乙型肝炎(CHB)中,在病毒清除和肝细胞损伤中均起着重要作用。我们对疾病自然史的认识的进步导致了感染的主要阶段的重新定义,“高复制,低炎症”阶段现已取代以前所谓的“免疫耐受”阶段和“非复制阶段”取代以前所谓的“非活动运营商”阶段。与先前的观点认为HBV通过利用新生儿免疫系统的不成熟来建立慢性感染的观点相反,经过训练的免疫力的新发现表明宿主在出生后已经有些“成熟”,并且实际上具有很强的免疫反应能力,可能会改变未来的乙肝治疗策略。尽管现有疗法可有效减少病毒载量和坏死性炎症,通常可使患者恢复到接近正常的健康水平,但除非极少数情况,否则它们无法治愈,而且在许多患者中,病毒血症在停止治疗后会反弹。现在,研究人员面临着挑战,需要设计出可以消除感染的疗法,尤其要着重于消除病毒cccDNA在肝细胞核中的持久性。在慢性乙型肝炎的背景下,“治愈”的新定义正在出现,例如“功能性”和“病毒性”治愈,其定义为稳定的非治疗性病毒血症和抗原血症的非治疗抑制,以及血清ALT和其他肝功能的正常化。相关的实验室测试。在对慢性乙型肝炎的复杂生物学认识的不断进步下,针对病毒和宿主因素以及以前无法获得治疗的途径的实验性新疗法的发展,这些方法可能在短期内导致病毒性治疗和功能性治疗经过长期随访。本文是“未完成的故事:从发现澳大利亚抗原到开发新的治疗乙型肝炎的疗法”抗病毒研究研讨会的一部分。 (C)2015 Elsevier B.V.保留所有权利。

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