Park Jiyoon, Sayed Amr, Nasir Syed Alishan, Lim Joseph K
Division of Gastroenterology, Norwalk Hospital, Norwalk, CT 06856, United States.
Section of Digestive Diseases and Yale Liver Center, Yale University School of Medicine, New Haven, CT 06520, United States.
World J Virol. 2025 Jun 25;14(2):102673. doi: 10.5501/wjv.v14.i2.102673.
Chronic hepatitis delta virus (HDV) represents a rare but important co-infection in approximately 5% of patients with chronic hepatitis B virus (HBV) infection, and is associated with significant morbidity and mortality due to an increased risk for liver cirrhosis, liver failure, and hepatocellular carcinoma relative to HBV monoinfected individuals. The current treatment of chronic HDV infection includes the off-label use of pegylated interferon (IFN), which is limited by poor safety, tolerability, and efficacy. Guidelines of the major international liver organizations such as the American Association for the Study of Liver Diseases, European Association for the Study of the Liver, and Asian Pacific Association for the Study of the Liver provide recommendations for contemporary diagnosis and management of chronic HDV infection, including the incorporation of bulevirtide, a newly licensed antiviral agent in Europe. Significant unmet medical needs remain in the treatment of HDV, and recent advances in drug development offer hope for meaningful advances in drug therapy which may improve virologic response rates and clinical outcomes. This review summarizes trial design and available efficacy data from key phase 2 and 3 trials for investigational therapies including entry inhibitors (bulevirtide), prenylation inhibitors (lonafarnib), novel IFNs (peginterferon lambda), RNA interference molecules (JNJ-3989, elebsiran), monoclonal antibodies (tobevibart), and nucleic acid polymers (REP2139), and addresses future directions in HDV pharmacotherapy.
慢性丁型肝炎病毒(HDV)感染在约5%的慢性乙型肝炎病毒(HBV)感染者中较为罕见但很重要,与肝硬化、肝衰竭和肝细胞癌风险增加相关,相对于单纯HBV感染个体,其发病率和死亡率更高。目前慢性HDV感染的治疗包括使用聚乙二醇化干扰素(IFN),但存在安全性、耐受性和疗效不佳的问题。美国肝病研究协会、欧洲肝脏研究协会和亚太肝脏研究协会等主要国际肝脏组织的指南为慢性HDV感染的当代诊断和管理提供了建议,包括纳入欧洲新获批的抗病毒药物布立伏定。HDV治疗中仍存在重大未满足的医疗需求,药物研发的最新进展为药物治疗取得有意义的进展带来了希望,这可能提高病毒学应答率和临床结局。本综述总结了关键2期和3期试验的试验设计和可用疗效数据,这些试验涉及的研究性治疗药物包括进入抑制剂(布立伏定)、异戊二烯化抑制剂(洛那法尼)、新型干扰素(聚乙二醇化λ干扰素)、RNA干扰分子(JNJ-3989、elbsiran)、单克隆抗体(tobevibart)和核酸聚合物(REP2139),并探讨了HDV药物治疗的未来方向。