Flares on and off therapy during chronic HBV infection: Pathogenesis, significance and management

D. Amarapurkar
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引用次数: 4

Abstract

Approximately 400 million people worldwide are chronically infected with the hepatitis B virus (HBV). Chronic infection with HBV can lead to progressive liver diseases including cirrhosis, liver failure, and hepatocellular carcinoma. During treatment of chronic hepatitis B (CHB) patients, flares of inflammatory activity are a well known phenomenon. Flares can be life threatening but have also been associated with virological response. While, interferon induced flares have been attributed to the stimulatory effect of IFN, and may precede HBeAg seroconversion, Lamivudine related flares are seen during treatment and after withdrawal of lamivudine, which are probably caused by reoccurrence of HBV replication, and have been associated with decompensation of liver disease. These flares play an important role in the treatment with Peg-IFN α-2b alone or in combination with lamivudine, and patients with pre-existing cirrhosis are at greater risk for experiencing a flare. Furthermore, host induced flares but not virus induced flares may herald a response to therapy. For optimisation of treatment, it is necessary to understand the virological and immunological mechanisms which induce the specific flare patterns. This article reviews the pathogenesis, significance and management of flares encountered during and after cessation of treatment of patients with chronic HBV infection.
慢性HBV感染治疗前后的耀斑:发病机制、意义和管理
全世界约有4亿人慢性感染乙型肝炎病毒(HBV)。慢性HBV感染可导致进行性肝病,包括肝硬化、肝功能衰竭和肝细胞癌。在慢性乙型肝炎(CHB)患者的治疗过程中,炎症活动的爆发是一个众所周知的现象。耀斑可危及生命,但也与病毒学反应有关。虽然干扰素诱导的急性发作归因于IFN的刺激作用,并可能在HBeAg血清转化之前发生,但在拉米夫定治疗期间和停药后出现拉米夫定相关的急性发作,这可能是由HBV复制的再次发生引起的,并与肝脏疾病代偿失调有关。这些耀斑在Peg-IFN α-2b单独或与拉米夫定联合治疗中起重要作用,并且已有肝硬化的患者经历耀斑的风险更大。此外,宿主诱导的耀斑而不是病毒诱导的耀斑可能预示着对治疗的反应。为了优化治疗,有必要了解引起特定耀斑模式的病毒学和免疫学机制。本文综述了慢性乙型肝炎病毒感染患者在治疗期间和停止治疗后遇到的耀斑的发病机制,意义和处理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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