Division of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
CRC "A. M. and A. Migliavacca" Center for Liver Disease, Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy.
Viruses. 2022 Oct 29;14(11):2404. doi: 10.3390/v14112404.
Chronic infection with hepatitis B virus (HBV) represents one of the main causes of the development of cirrhosis and its complications. Treatment with potent third-generation nucleos(t)ide analogues (NUCs) results in >99% HBV DNA undetectability, and prevents fibrosis progression and liver-related complications. However, NUCs are not able to induce the so-called functional cure, which is hepatitis B surface antigen (HBsAg) loss and anti-HBs seroconversion. Consequently, NUC treatment is currently intended as being long-term or lifelong, resulting in the need for clinical monitoring and potentially suffering from compliance issues. Consequently, drug development in HBV has the goal of developing new agents in order to achieve a functional cure for HBV. Currently, the three main strategies include the following: inhibition of viral replication, inhibition of viral antigens, and immune modulation. This review summarizes the most recent updates concerning HBV compounds among these three main classes.
慢性乙型肝炎病毒(HBV)感染是肝硬化及其并发症发展的主要原因之一。使用强效第三代核苷(酸)类似物(NUC)治疗可使 HBV DNA 检测不到>99%,并可阻止纤维化进展和肝脏相关并发症。然而,NUC 不能诱导所谓的功能性治愈,即乙型肝炎表面抗原(HBsAg)消失和抗-HBs 血清转换。因此,NUC 治疗目前被认为是长期或终身的,需要进行临床监测,并可能存在依从性问题。因此,HBV 的药物研发旨在开发新的药物,以实现 HBV 的功能性治愈。目前,主要有三种策略,包括抑制病毒复制、抑制病毒抗原和免疫调节。本综述总结了这三种主要类别中 HBV 化合物的最新进展。