实用肝脏病杂志 ›› 2016, Vol. 19 ›› Issue (1): 25-28.doi: 10.3969/j.issn.1672-5069.2016.01.007

• 乙型肝炎 • 上一篇    下一篇

恩替卡韦联合免疫制剂治疗免疫耐受期乙型肝炎病毒携带者疗效探讨

赵和平, 侯田青, 丁保华, 张自然, 李靖, 刘晓蕾, 邵丹丹, 郭世民   

  1. 471031 河南省洛阳市 解放军第150医院感染病科
  • 收稿日期:2015-05-14 出版日期:2016-01-10 发布日期:2016-02-04
  • 通讯作者: 郭世民,E-mail:190880818@qq.com
  • 作者简介:赵和平,男,主任医师。主要从事各种疑难重症肝病的诊疗研究。E-mail:ZhaoHP150.@sina.com

Efficacy of entecavir and immunotherapy in treatment of hepatitis B virus carriers

Zhao Heping, Hou Tianqing, Ding Baohua, Zhang Ziran, Li jing, Liu Xiaolei, ShaoDandan, Guo Shimin   

  1. Department of Infectious Diseases,150th Hospital of Chinese People's Liberation Army,Luoyang 471031,Henan Provence,China
  • Received:2015-05-14 Online:2016-01-10 Published:2016-02-04

摘要: 目的观察恩替卡韦联合免疫制剂治疗免疫耐受期乙型肝炎病毒(HBV)携带者的临床疗效。方法按就诊顺序编号将66例HBV携带者随机分为治疗组33例和对照组33例。给予治疗组恩替卡韦联合重组乙肝疫苗(CHO细胞)20 μg、重组人白细胞介素-II 20万单位和重组人粒细胞集落刺激因子75 μg三角肌皮下注射,1次/m,疗程为3年;对照组只接受单纯的恩替卡韦治疗,疗程也为3年。治疗前后常规检测血清丙氨酸氨基转移酶(ALT)、HBV DNA、血清HBV标记物的变化。结果在治疗结束时,治疗组患者血清HBeAg阴转率、HBeAg血清转换率和HBV DNA阴转率分别为33.3%、24.2%和75.7%,显著高于对照组的12.1%、6.0%和51.5% (P<0.05);在治疗结束后6个月时,治疗组血清HBeAg阴转率、HBeAg血清转换率和HBV DNA阴转率分别为42.3%、27.2%和78.7%,也显著高于对照组的12.1%、6.0%和45.4% (P<0.05);在治疗过程中两组部分患者ALT升高,其中治疗组为42.3%,显著高于对照组的9.0%(P<0.05)。结论核苷类药物联合免疫制剂治疗HBV携带者,在部分人群能打破免疫耐受,并获得病毒学清除。

关键词: 乙型肝炎病毒携带者, 免疫耐受, 恩替卡韦, 免疫疗法

Abstract: Objective To observe the clinical efficacy of combination of entecavir(ETV) and immunotherapy in the treatment of hepatitis B virus carriers. Method 66 hepatitis B virus carriers were randomly assigned into treatment group and control group with 33 in each group. Individuals in the treatment group were treated by ETV and hepatitis B vaccine,rIL-2,and G-CSF,and those in the control group were treated with ETV alone. The regimen lasted for three years in both groups. Before and after the treatment,serum level of ALT,HBV DNA,HBeAg,HBeAb,HBsAg were detected routinely. Results At the end of the treatment,negative rate of serum HBeAg in the treatment group was 33.3%,significantly higher than that in the control group(12.1%,P<0.05);the seroconversion rate of HBeAg to anti-HBe was 24.2% in the treatment group,significantly higher than that in the controls(6.0%,P<0.05);the serum HBV DNA loss in treatment group was 75.7%,significant higher than that in the control group(51.5%,P<0.05);At the end of six months after the discontinuation of the treatment,the negative rate of serum HbeAg was 42.4%,the seroconversion of HbeAg to anti-HBe rate was 27.2%,and the serum HBV DNA loss was 78.7% in the treatment group,all significantly higher than those in the controls(12.1%,6.0% and 45.4%,respectively,P<0.05);serum levels of ALT were elevated in 42.3% of individuals in treatment group, significantly higher than that in the controls(9.0%,P<0.05). Conclusion The clinical efficacy of combination therapy with nucleoside analogues and immune-modulating agents are promising,which might break the state of immune tolerance in some hepatitis B virus carriers.

Key words: Hepatitis B virus carriers, Entecavir, Immune tolerance, Immune-modulating agents