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Role of antiviral therapy in the natural history of hepatitis B virus-related chronic liver disease

机译:抗病毒治疗在乙型肝炎病毒相关的慢性肝病自然史中的作用

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摘要

Hepatitis B virus (HBV) infection is a dynamic state of interactions among HBV, hepatocytes, and the host immune system. Natural history studies of chronic hepatitis B (CHB) infection have shown an association between active viral replication and adverse clinical outcomes such as cirrhosis and hepatocellular carcinoma. The goal of therapy for CHB is to improve quality of life and survival by preventing progression of the disease to cirrhosis, decompensation, end-stage liver disease, hepatocellular carcinoma (HCC) and death. This goal can be achieved if HBV replication is suppressed in a sustained manner. The accompanying reduction in histological activity of CHB lessens the risk of cirrhosis and of HCC, particularly in non-cirrhotic patients. However, CHB infection cannot be completely eradicated, due to the persistence of covalently closed circular DNA in the nucleus of infected hepatocytes, which may explain HBV reactivation. Moreover, the integration of the HBV genome into the host genome may favour oncogenesis, development of HCC and may also contribute to HBV reactivation.
机译:乙型肝炎病毒(HBV)感染是HBV,肝细胞和宿主免疫系统之间相互作用的动态状态。慢性乙型肝炎(CHB)感染的自然史研究表明,活跃的病毒复制与不良临床结局(例如肝硬化和肝细胞癌)之间存在关联。 CHB的治疗目标是通过预防疾病发展为肝硬化,代偿失调,终末期肝病,肝细胞癌(HCC)和死亡来改善生活质量和生存。如果以持续方式抑制HBV复制,则可以实现此目标。随之而来的CHB组织学活性降低可降低肝硬化和HCC的风险,特别是在非肝硬化患者中。但是,由于被感染的肝细胞核中共价闭合的环状DNA持续存在,因此无法完全消除CHB感染,这可以解释HBV的重新激活。此外,将HBV基因组整合到宿主基因组中可能有助于癌发生,HCC的发生,也可能有助于HBV的重新激活。

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