INSERM U1052, UMR CNRS 5268, Cancer Research Center of Lyon, F-69003 Lyon, France.
Antiviral Res. 2012 Nov;96(2):256-9. doi: 10.1016/j.antiviral.2012.09.006. Epub 2012 Sep 19.
The treatment of chronic hepatitis B remains limited to monotherapy with pegInterferon-alpha or one of 5 different nucleoside analogues (NUC). While viral suppression can be achieved in approximately 95% of patients with new-generation NUCs, the rate of HBeAg seroconversion ranges from only 20% with NUCs to 30% with pegInterferon-alpha. HBsAg loss is achieved in only 10% of patients with both classes of drugs after a follow-up of 5years. Attempts to improve the response by administering two different NUCs or a combination of NUC and pegInterferon-alpha have been unsuccessful. This situation has led researchers to investigate a number of steps in the HBV replication cycle as potential targets for new antiviral drugs. Novel targets and compounds could readily be evaluated in in vitro and in vivo models of HBV infection. The addition of one or more new drugs to the current regimen should offer the prospect of markedly improving the response to therapy, reducing the future burden of drug resistance, cirrhosis and hepatocellular carcinoma.
慢性乙型肝炎的治疗仍然局限于聚乙二醇干扰素-α或 5 种不同核苷类似物(NUC)的单药治疗。虽然新代 NUC 可使约 95%的患者实现病毒抑制,但 HBeAg 血清学转换率仅为 NUC 的 20%,聚乙二醇干扰素-α的 30%。在 5 年的随访中,只有这两类药物的 10%的患者可实现 HBsAg 丢失。通过给予两种不同的 NUC 或 NUC 和聚乙二醇干扰素-α联合治疗以提高应答的尝试均未成功。这种情况促使研究人员研究乙型肝炎病毒复制周期中的多个步骤作为新抗病毒药物的潜在靶点。新型靶标和化合物可以在乙型肝炎病毒感染的体外和体内模型中进行易于评估。在现有方案中添加一种或多种新药应该有望显著提高治疗反应,降低未来耐药、肝硬化和肝细胞癌的负担。