期刊文献+

重组集成干扰素α体外抗病毒的药效学研究 被引量:3

Inhibitory effects of recombinant consensus interferon α on different viruses in vitro
下载PDF
导出
摘要 目的:观察一种新型重组集成干扰素α(NIFN-conα)对流感病毒甲型和乙型、单纯疱疹病毒Ⅰ型和Ⅱ型、柯萨奇病毒B1和B3的抑制作用。方法:应用细胞病变抑制法,以已上市的重组集成干扰素α(干复津)及干扰素α作为阳性对照,观察不同浓度的NIFN-conα对不同病毒感染绿猴肾细胞(Vero)和狗肾细胞(MDCK)的抑制作用。结果:NIFN-conα对MDCK细胞和Vero细胞的TD50分别为(>250±0)μg/ml和(>192±0)μg/ml。对单纯疱疹Ⅰ型和Ⅱ型病毒的IC50分别是(2.8×10-4±8.5×10-5)和(1.8×10-4±8.5×10-5)μg/ml;对柯萨奇病毒B1和B3的IC50分别是(8.8×10-8±1.4×10-8)和(1.5×10-7±4.2×10-8)μg/ml,抑制流感病毒甲型和乙型的IC50分别是(2.5×10-2±1.2×10-2)和(>10±0)μg/ml。结论:NIFN-conα与干复津一样对单纯疱疹病毒、柯萨奇病毒和流感病毒均具有明显的抑制作用,与干扰素α相比,对流感病毒的抑制作用较弱,但对单纯疱疹病毒和柯萨奇病毒的抑制作用优于干扰素α。 Objective. To investigate the antiviml activity of one of the new recombinant consensus interferon α (NIFN-con α) in vitro, Methods: The cytopathic-effect inhibition assay was applied in this study to investigate the antiviral activity of this drug as well as the other IFN-con α (Infergen) and IFN-α as positive control. Vero cells and MDCK cells were infected by different viruses respectively and were cultured with serial dilutions of NIFN- con α. Results: The TD50 of NIFN-con α for MDCK cells and Veto cells was ( 〉 250± 0)μg/ml and 〉 192± 0 μg/ml, respectively. The IC50 of NIFN-con a for Herpes vires type 1 and type 2 was (2.8 × 10^-4 ± 8.5 × 10^-5 ) and ( 1.8 × 10^- 4 ± 8.5 × 10^- 5 )μg/ml, respectively, for coxsackie virus B 1 and B3 was (8.8 × 10^-8s ± 1.4 × 10^- 8 ) and ( 1.5 × 10^- 7 ± 4.2 × 10^- 7 ) μg/ml, respectively and for influenza virus A and B was (2.5 × 10^- 2 ± 1.2 × 10^- 2 ) and ( 〉 10 ± 0)μg/ml, respectively. Conclusion: The new drug has similar antiviral activities with Infergen, and compare with interferon a, it has more effective antiviral activities for HSV and coxsackie virus except for influenza viruses.
出处 《山东大学学报(医学版)》 CAS 北大核心 2006年第8期831-833,839,共4页 Journal of Shandong University:Health Sciences
关键词 干扰素Ⅰ型 重组 集成 细胞病变抑制法 抗病毒药 正粘病毒科 单纯疱疹病毒属 柯萨奇病毒 Interferon Ⅰ, recombinant, consensus Cytopathic-effect inhibition assay Antiviral drug Orthomyxcviridae Herpesvimses Coxsackie virus
  • 相关文献

参考文献7

  • 1Blatt LM,Davis JM,Klein SB,et al.Thebiologic activity and molecular characterization of anovel synthetic interferon-alpha species,consensusinterferon[J].J Interferon Cytokine Res,1996,16:489-499.
  • 2Ozes ON,Reiter Z,Klein S,et al.A comparison of interferon-con1 with natural recombinant interferons-α:antiviral,antiproliferative,and natural killer-inducing activities[J].J Interferon Res,1992,12:55-59.
  • 3Fish EN,Banerjee K,Stebbing N.The role of three domains in the biological activity of human interferon-α[J].J Interferon Res,1989,9:97-114.
  • 4Heathcote EJL,Keeffe EB,Lee SS,et al.Re-treatment of chronic hepatitis C with consensus interferon[J].Hepatology,1998,27(4):1 136-1 143.
  • 5Tong MJ,Blatt LM,Resser KJ,et al.Treatment of chronic hepatitis C virus infection with recombinant consensus interferon[J].J Interferon and Cytokine Res,1998,18:81-86.
  • 6Fish EN.Definition of receptor binding domains in interferon-α[J].J Interferon Res,1992,12:257-266.
  • 7Arnheiter H,Ohno M,Smith M,et al.Orientation of a human leukocyte interferon molecule on its cell surface receptor:Carboxyl terminus remains accessible to a monoclonal antibody made against a synthetic interferon fragment[J].Proc Natl Acad Sci USA,1983,80:2539-2543.

同被引文献26

引证文献3

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部