Department of Medicine, School of Clinical Medicine, Queen Mary Hospital, Pokfulam Road 102, Hong Kong, China; State Key Laboratory of Liver Research, 7/F, HK Jockey Club Building of Interdisciplinary Research, 5 Sassoon Road, Pokfulam, Hong Kong, China.
Department of Medicine, School of Clinical Medicine, Queen Mary Hospital, Pokfulam Road 102, Hong Kong, China.
Clin Liver Dis. 2023 Nov;27(4):877-893. doi: 10.1016/j.cld.2023.05.004. Epub 2023 Jul 6.
Currently approved treatment of patients with chronic hepatitis B infection is insufficient to achieve functional cure. Numerous new compounds are identified, and among many, capsid assembly modulators (CAMs) and nucleic acid polymers (NAPs) are 2 classes of virus-directing agents in clinical development. CAMs interfere with viral pregenomic RNA encapsidation and are effective in viral load reduction but have limited effects on hepatitis B surface antigen (HBsAg). NAPs prevent HBsAg release from hepatocytes and induce intracellular degradation, leading to potent suppression of serum HBsAg when combined with nucleoside analogues and pegylated interferon demonstrated by initial data, but awaiting further confirmation studies.
目前,慢性乙型肝炎感染患者的治疗方法尚不能达到功能性治愈。已经鉴定出许多新的化合物,其中衣壳组装调节剂(CAMs)和核酸聚合物(NAPs)是临床开发中的 2 类病毒定向药物。CAMs 干扰病毒前基因组 RNA 的包裹,在降低病毒载量方面有效,但对乙型肝炎表面抗原(HBsAg)的影响有限。NAPs 阻止 HBsAg 从肝细胞中释放,并诱导细胞内降解,与初始数据显示的核苷类似物和聚乙二醇干扰素联合使用时,可有效抑制血清 HBsAg,但还需要进一步的确认研究。