实用肝脏病杂志 ›› 2024, Vol. 27 ›› Issue (5): 677-680.doi: 10.3969/j.issn.1672-5069.2024.05.008

• 病毒性肝炎 • 上一篇    下一篇

聚乙二醇干扰素α-2b联合恩替卡韦治疗HBeAg阳性慢性乙型肝炎患者疗效研究*

彭麟, 杨春, 李兴泉   

  1. 404100 重庆市綦江区人民医院感染病科(彭麟,李兴泉);重庆医科大学附属第一医院感染病科(杨春)
  • 收稿日期:2024-03-04 出版日期:2024-09-10 发布日期:2024-09-09
  • 通讯作者: 李兴泉,E-mail:2761838146@qq.com
  • 作者简介:彭麟,女,40岁,大学本科,副主任医师。E-mail:penglin1231232023@163.com
  • 基金资助:
    *重庆市卫健委科研基金资助项目(编号:2021JH031400)

Peginterferon alpha and entecavir combination in treatment of patients with serum HBeAg-positive chronic hepatitis B

Peng Lin, Yang Chun, Li Xingquan   

  1. Department of Infectious Diseases, District People's Hospital, Qijiang 404100, Chongqing, China
  • Received:2024-03-04 Online:2024-09-10 Published:2024-09-09

摘要: 目的 观察比较聚乙二醇干扰素α-2b(Peg-IFN-α)联合恩替卡韦治疗血清HBeAg阳性的慢性乙型肝炎(CHB)患者的疗效。方法 2019年1月~2022年1月我院收治的279例血清HBeAg阳性的CHB患者,被分为3组,每组93例,分别给予恩替卡韦口服治疗、Peg-IFN-α皮下注射治疗或恩替卡韦联合Peg-IFN-α治疗,均持续治疗48 w,评估疗效。常规检测血清生化学、血清学和病毒学指标。 结果 在治疗48 w末,联合组HBeAg转阴率和HBeAg血清转换率分别为32.3%和21.5%,Peg-IFN-α治疗组分别为22.6%和15.1%,而恩替卡韦治疗组则无血清HBeAg转阴或HBeAg血清转换者,联合组尚有一些零星的病例发生HBsAg转阴(3.2%)或HBsAg血清转换(2.2%);联合组血清HBsAg和HBeAg水平分别为(1.9±0.3)lg s/co和(0.5±0.1)lg s/co,Peg-IFN-α治疗组分别为(2.2±0.2)lg s/co和(0.6±0.1)lg s/co,均显著低于恩替卡韦治疗组【分别为(3.6±0.2)lg s/co和(1.3±0.2)lg s/co,P<0.05】,而联合组和恩替卡韦治疗组血清HBV DNA载量均显著低于Peg-IFN-α治疗组(P<0.05);联合组血清ALT和AST水平分别为(30.9±4.5)U/L和(28.4±5.3)U/L,恩替卡韦治疗组分别为(31.5±3.6)U/L和(32.3±4.7)U/L,均显著低于Peg-IFN-α治疗组【分别为(48.1±4.2)U/L和(42.7±5.0)U/L,P<0.05】。 结论 联合应用恩替卡韦和Peg-IFN-α治疗血清HBeAg阳性的CHB患者可能获得更好的血清学转换率,在优势人群可能获得功能性治愈,值得深入研究。

关键词: 慢性乙型肝炎, 聚乙二醇干扰素α-2b, 恩替卡韦, 治疗, 功能治愈

Abstract: Objective The aim of this study was to investigate antiviral efficacy of peginterferon alpha (Peg-IFN-α) and entecavir (ETV) combination in treatment of patients with serum HBeAg-positive chronic hepatitis B (CHB). Methods A total of 279 patients with serum HBeAg-positive CHB were enrolled in this study between January 2019 and January 2022, and were randomly divided into three groups, with 93 cases in each group. Oral entecavir, subcutaneous injection of Peg-IFN-α, or combination of entecavir and Peg-IFN-α were given, and antiviral regimen lasted for 48 weeks. Serum biochemical, serological and virological responses were routinely assessed. Results By end of 48 week treatment, serum HBeAg negative rate and seroconversion rate in combination group were32.3% and 21.5%, in Peg-IFN-α group were 22.6% and 15.1%, while in entecavir group, no serum HBeAg negative and no serum HBeAg conversion; also in combination group, 3.2% of patients had serum HBsAg negative and 2.2% of them had serum HBsAg seroconversion; serum HBsAg and HBeAg levels in combination group were (1.9±0.3)lg s/co and (0.5±0.1)lg s/co, in Peg-IFN-α group were (2.2±0.2)lg s/co and (0.6±0.1)lg s/co, both significantly lower than [(3.6±0.2)lg s/co and (1.3±0.2)lg s/co, P<0.05] in entecavir group, while serum HBV DNA loads in combination and entecavir groups were much lower than in Peg-IFN-α group (P<0.05); serum ALT and AST levels in combination group were (30.9±4.5)U/L and (28.4±5.3)U/L, in entecavir group were (31.5±3.6)U/L and (32.3±4.7)U/L, both significantly lower than [(48.1±4.2)U/L and (42.7±5.0)U/L, respectively, P<0.05] in Peg-IFN-α-treated group. Conclusion Combination of entecavir and Peg-IFN-α in treatment of patients with serum HBeAg-positive CHB could gain satisfactory serum HBeAg negative and seroconversion rates, and in dominant population might obtain functional cure.

Key words: Hepatitis B, Peginterferon alpha, Entecavir, Therapy, Functional cure