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不同剂量干扰素治疗慢性乙型肝炎时血清2′,5′-寡腺苷酸合成酶活性的变化 被引量:2

Changes of Serum 2', 5'-Oligoadenylate Synthetase Activity during Different Doses Interferon Treatment for Chronic Hepatitis B
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摘要 目的:观察不同剂量干扰素治疗慢性乙型病毒性肝炎时血清2′,5′-寡腺苷酸合成酶(2′,5′-OAS)的变化,了解细胞抗病毒状态建立与乙肝病毒复制的关系。方法:32例慢性乙肝患者随机分为3蛆,即1MU干扰素腹腔注射11例(治疗Ⅰ组),3MU干扰素皮下注射11例(治疗Ⅱ组),分别连续注射5天,以后每周3次,共16周,并与不用干扰素治疗的10例(对照组)作对比,通过2′,5′-OAS、ALT、HBeAg、HBV-DNA(PCR法)连续检测,评价治疗反应。结果:疗程结束时,两治疗组和对照组ALT均下降,3组差异无显著性(P>0.05)。治疗Ⅰ组和治疗Ⅱ组2′,5′-OAS的活性均增加,治疗Ⅰ组在疗程结束时达峰值,治疗Ⅱ组在疗程早期就明显升高,而对照组无升高(P<0.05)。2′,5′-OAS的增幅水平与HBeAg、HBV-DNA的阴转呈相关性。结论,2′,5′-OAS可能是监测干扰素治疗慢性乙型肝炎疗效的有效指标。 Aim:To observe the changes of serum 2', 5'-oligoadenylate synthetase (2', 5'-OAS) activity in patients with chronic hepatitis B when different doses interferon (IFN) were used, and to comprehend the relation between antiviral state established in cells and replication of hepatitis B virus. Methods: 32 patients with chronic hepatitis B were assigned randomly to three groups. Treatment group Ⅰ consisting of 11 patients received 1 megaunit (MU) IFN by ab-dominocentesis daily for 5 days, and then three times weekly for 16 weeks. Treatment group Ⅱ consisting of 11 patients, too, received 3 MU IFN by subcutaneous injection daily for 5 days, and then three times weekly for 16 weeks. control group (10 cases) received no IFN treatment. Response was predefined as loss of HBeAg, HBV-DNA (PCR) and changes of serum alanine amino-transferase (ALT). 2', 5'-OAS was evaluated as potential predictors of response to therapy. Results: The ALT levels in both treatment groups and control group decreased at the end of course of treatment. There were no significant difference in three groups (P>0. 05). 2', 5'-OAS activities increased in both treatment groups, but not in the control group (P<0. 05). There were changes of different curves of 2', 5'-OAS in treatment group Ⅰ and Ⅱ. The peak of 2', 5'-OAS activity was found at the end of therapy of group Ⅰ , and the early stage of therapy of gropuⅡ. 2', 5'-OAS levels were correlated with returned negative of HBV-DNA and HBeAg. Conclusion: This study suggests that 2', 5'-OAS may be a useful marker to monitor IFN efficacy during treatment and to predict the clinical respose.
出处 《中西医结合肝病杂志》 CAS 1997年第1期8-11,共4页 Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases
关键词 乙型肝炎 寡腺苷酸 合成酶 干扰素 Chronic Hepatitis B 2' 5'-Oligoadenylate Synthetase Interferon
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  • 1钱美宝,缪鹤章,吴惟一,屠士行,何建军,朱东.干扰素治疗慢性病毒性肝炎近期疗效观察[J].肝脏病杂志,1995,3(1):41-41. 被引量:2
  • 2张春英,殷珊,王豪,冯百芳,陶其敏.α-干扰素和香菇多糖对乙型肝炎病毒感染者白细胞介素-2受体表达的影响[J].中华实验和临床病毒学杂志,1996,10(2):128-131. 被引量:7
  • 3何生松,黄华芳.慢性乙型肝炎患者血清肿瘤坏死因子受体检测及与干扰素治疗的关系[J].中西医结合肝病杂志,1997,7(1):5-7. 被引量:4
  • 4Hajnicka V, Fuchsberger N, Liptakova H, et al, Interferon-omega suppresses hepatitis B surface antigen production in human hepatoma cell line. Acta Virol,1996; 40(4):221-222
  • 5张定风.干扰素抗肝炎病毒治疗的机理及近况.中华医学会肝脏病学分会1999全国肝脏疾病临床学术研讨会论文汇编.青岛,1999;1-10
  • 6Action against viruses. In: Eddleston ALWF, Dixon. Interferon in the treatment of chronic virus infection of the liver. Cheshire: Pennine press. Ed2. 1990;16
  • 7Fernandez M, Quiroga JA, Martin J, et al. Impaired interferon induction of human MxA protein in chronic hepatitis B virus infection.J Med Virol, 1997;51(4):332-337
  • 8Rosmorduc O, Sirma H, Soussan P, et al. Inhibition of interferon-inducible MxA protein expression by hepatitis B virus capsid protein.J Gen Virol, 1999;80(pt5): 1253-1262
  • 9Guidotti LG, McClary H, Loudis JM, Chisari FV. Nitric oxide inhibits hepatitis B virus replication in the livers of transgenic mice. J Exp Med, 2000;191(7):1247-1252
  • 10Nakao K, Nakata K, Yamashita M, et al. P48(ISGF-3gamma) is involved in interferon-alpha-induced suppression of hepatitis B virus enhancer-1 activity. J Biol Chem, 1999; 274(40):28075-28078

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