Liver Unit and its Molecular Biology Laboratory, National and Kapodistrian University of Athens, Evgenidion Hospital of Athens, Athens, Greece.
J Clin Transl Hepatol. 2014 Dec;2(4):285-91. doi: 10.14218/JCTH.2014.00026. Epub 2014 Dec 15.
This review article is an update of the current treatment strategies available for chronic hepatitis B. In addition to achieving on-therapy clinical remission and suppression of HBV replication without resistance, the ultimate goal of therapy is the development of sustained remission and HBsAg loss after discontinuation of treatment. This is the closest possible to cure outcome for hepatitis B virus (HBV) infection. These goals can be achieved by response-guided courses of pegylated interferon (peg-IFN)-alpha at rates higher than 30%, both in hepatitis B e antigen (HBeAg)-positive and HBeAg-negative patients. Review of the data regarding discontinuation of long term NA treatment in HBeAg-negative patients revealed that stopping such therapy is safe with high rates of sustained off treatment responses that appear to be immunologically induced. Decreasing hepatitis B surface antigen (HBsAg) titers under therapy to <500, particularly <100 IU/mL, and adding a course of peg-IFN to ongoing long term nucleos(t)ide analogue (NA) therapy increase the percentage of sustained responses following discontinuation of NA treatment.
这篇综述文章更新了目前用于慢性乙型肝炎的治疗策略。除了在治疗过程中实现临床缓解和抑制无耐药性的 HBV 复制之外,治疗的最终目标是在停药后实现持续缓解和 HBsAg 丢失。这是乙型肝炎病毒 (HBV) 感染最接近治愈的结果。通过应答指导的聚乙二醇干扰素 (peg-IFN)-α 疗程,可以在 HBeAg 阳性和 HBeAg 阴性患者中实现这一目标,其比例高于 30%。回顾关于 HBeAg 阴性患者长期 NA 治疗停药的数据显示,停止这种治疗是安全的,停药后持续应答率较高,似乎是免疫诱导的。在治疗过程中降低 HBsAg 滴度至 <500,特别是 <100 IU/mL,并在正在进行的长期核苷(酸)类似物 (NA) 治疗中添加 peg-IFN 疗程,可增加 NA 治疗停药后持续应答的百分比。