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乙型肝炎病毒感染

Hepatitis B virus infection.

作者信息

Liaw Yun-Fan, Chu Chia-Ming

机构信息

Liver Research Unit, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taipei, Taiwan.

出版信息

Lancet. 2009 Feb 14;373(9663):582-92. doi: 10.1016/S0140-6736(09)60207-5.

Abstract

Since the introduction of the hepatitis B vaccine and other preventive measures, the worldwide prevalence of hepatitis B infection has fallen. However, chronic infection remains a challenging global health problem, with more than 350 million people chronically infected and at risk of hepatic decompensation, cirrhosis, and hepatocellular carcinoma. An improved understanding of hepatitis B virology, immunology, and the natural course of chronic infection, has identified hepatitis B virus replication as the key driver of immune-mediated liver injury and disease progression. The approval of potent oral antiviral agents has revolutionised hepatitis B treatment since 1998. Conventional and pegylated interferon alfa and nucleoside and nucleotide analogues are widely authorised treatments, and monotherapy with these drugs greatly suppresses virus replication, reduces hepatitis activity, and halts disease progression. However, hepatitis B virus is rarely eliminated, and drug resistance is a major drawback during long term therapy. The development of new drugs and strategies is needed to improve treatment outcomes.

摘要

自乙肝疫苗及其他预防措施问世以来,全球乙肝感染率已有所下降。然而,慢性感染仍是一个具有挑战性的全球健康问题,超过3.5亿人长期感染,面临肝失代偿、肝硬化和肝细胞癌的风险。对乙肝病毒学、免疫学以及慢性感染自然病程的深入了解,已确定乙肝病毒复制是免疫介导的肝损伤和疾病进展的关键驱动因素。自1998年以来,强效口服抗病毒药物的获批彻底改变了乙肝治疗。传统和聚乙二醇化干扰素α以及核苷和核苷酸类似物是广泛认可的治疗药物,这些药物单药治疗可极大地抑制病毒复制、降低肝炎活动度并阻止疾病进展。然而,乙肝病毒很少被清除,耐药性是长期治疗中的一个主要缺点。需要开发新的药物和策略来改善治疗效果。

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