Department of Gastroenterology and Hepatology, University Hospital Essen, University of Duisburg-Essen. Essen, Germany.
AIDS Rev. 2019;21(3):126-134. doi: 10.24875/AIDSRev.19000080.
Persistent coinfection with the hepatitis B/D viruses (HDV) represents the most severe form of viral hepatitis. Hepatitis D often leads to liver cirrhosis, hepatic decompensation, and hepatocellular carcinoma. The current treatment options are limited as only pegylated interferon-alpha (PEG-IFNa) has efficacy against HDV. However, treatment response is still unsatisfactory with 25-40% HDV RNA suppression after 1-2 years. In addition, late HDV RNA relapses have been described during long-term follow-up. Fortunately, new treatment options for patients with chronic hepatitis delta are now on the horizon. The hepatocyte entry inhibitor bulevirtide (formerly myrcludex B) and the farnesyl transferase inhibitor lonafarnib are currently explored in patients with chronic hepatitis delta in Phase 3 clinical studies. The nucleic acid inhibitor REP-2139-Ca and PEG-IFN-lambda are studied in Phase 2 trials. We here summarize data on the efficacy of these new antiviral drugs and the existing safety data on the treatment of HDV infection.
慢性乙型/丁型肝炎病毒(HDV)持续感染是最严重的病毒性肝炎形式。丁型肝炎常导致肝硬化、肝功能失代偿和肝细胞癌。目前的治疗选择有限,只有聚乙二醇干扰素-α(PEG-IFNα)对 HDV 有效。然而,治疗反应仍不理想,1-2 年后仅有 25-40%的 HDV RNA 得到抑制。此外,在长期随访中还描述了晚期 HDV RNA 复发。幸运的是,现在慢性丁型肝炎患者有了新的治疗选择。肝细胞进入抑制剂布乐韦肽(原称 myrcludex B)和法尼酯转移酶抑制剂 lonafarnib 目前正在 3 期临床试验中用于慢性丁型肝炎患者。核酸抑制剂 REP-2139-Ca 和 PEG-IFN-lambda 在 2 期试验中进行了研究。我们在这里总结了这些新型抗病毒药物的疗效数据和现有治疗 HDV 感染的安全性数据。