Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.
Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland.
Gastroenterology. 2019 Jan;156(2):461-476.e1. doi: 10.1053/j.gastro.2018.09.058. Epub 2018 Oct 18.
Hepatitis delta virus (HDV) infection of humans was first reported in 1977, and now it is now estimated that 15-20 million people are infected worldwide. Infection with HDV can be an acute or chronic process that occurs only in patients with an hepatitis B virus infection. Chronic HDV infection commonly results in the most rapidly progressive form of viral hepatitis; it is the chronic viral infection that is most likely to lead to cirrhosis, and it is associated with an increased risk of hepatocellular carcinoma. HDV infection is the only chronic human hepatitis virus infection without a therapy approved by the US Food and Drug Administration. Peginterferon alfa is the only recommended therapy, but it produces unsatisfactory results. We review therapeutic agents in development, designed to disrupt the HDV life cycle, that might benefit patients with this devastating disease.
人乙型肝炎病毒 delta 型(HDV)感染于 1977 年首次报道,目前估计全球有 1500 万至 2000 万人受到感染。HDV 的感染可以是急性或慢性的过程,仅发生在乙型肝炎病毒感染者中。慢性 HDV 感染通常导致最迅速进展的病毒性肝炎;它是最有可能导致肝硬化的慢性病毒感染,并与肝细胞癌的风险增加相关。HDV 感染是唯一一种未经美国食品和药物管理局批准的慢性人类肝炎病毒感染。聚乙二醇干扰素 alfa 是唯一被推荐的治疗方法,但效果并不理想。我们综述了正在开发的旨在破坏 HDV 生命周期的治疗药物,这些药物可能使患有这种毁灭性疾病的患者受益。