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