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陈芳,王艾平,申明强,陈默,许杨,王崧,粟永萍,程天民,王军平.人α防御素-5多肽体外抗单纯疱疹Ⅱ型病毒作用的研究[J].陆军军医大学学报(原第三军医大学学报),2010,32(18):1925-1928.
Chen Fang,Wang Aiping,Shen Mingqiang,Chen Mo,Xu Yang,Wang Song,Su Yongping,Cheng Tianmin,Wang Junping.Human α-defensins-5 against herpes simplex virus type 2 in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(18):1925-1928.
陈芳,王艾平,申明强,陈默,许杨,王崧,粟永萍,程天民,王军平.人α防御素-5多肽体外抗单纯疱疹Ⅱ型病毒作用的研究[J].陆军军医大学学报(原第三军医大学学报),2010,32(18):1925-1928. DOI:
Chen Fang,Wang Aiping,Shen Mingqiang,Chen Mo,Xu Yang,Wang Song,Su Yongping,Cheng Tianmin,Wang Junping.Human α-defensins-5 against herpes simplex virus type 2 in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(18):1925-1928. DOI:
目的 探讨人α防御素-5(human α-defensin-5, HD-5)多肽体外抗单纯疱疹Ⅱ型病毒(herpes simplex virus type 2, HSV-2)的作用及其机制。 方法 以绿猴肾细胞(Vero)为宿主细胞,采用CCK-8法首先分析10~200 μg/ml浓度范围内HD-5多肽的细胞毒性,再以HSV-2感染Vero细胞,分别于感染前后和感染的同时加入100 μg/ml 的HD-5多肽,72 h后测定细胞保护率,结合细胞病变效应观察,分析HD-5抗HSV-2的作用效果和起效环节,并通过改变培养基中血清的浓度,观察血清对HD-5抗病毒作用的影响。 结果 在100 μg/ml 浓度以内
HD-5多肽几乎无细胞毒性,提前或同时加入HD-5多肽可以显著抑制HSV-2病毒引起的细胞病变反应、提高细胞保护率(P0.01),而在HSV-2感染2 h后加入HD-5多肽对Vero细胞的保护作用不明显(P0.05);血清浓度会显著影响HD-5多肽的抗HSV-2活性,血清浓度越高,HD-5多肽对细胞的保护率越低。 结论 HD-5多肽在体外具有显著的抗HSV-2感染活性,其作用机制主要是通过干扰病毒对细胞的粘附、侵入而发挥作用。
Objective To investigate the effects of human α-defensin-5 (HD-5) against herpes simplex virus type 2 (HSV-2) in Vero cells cultured in vitro. Methods Cytotoxicity of HD-5 at various concentrations (10 to 200 μg/ml) on cultured Vero cells was determined by CCK-8 assay. HD-5 of 100 μg/ml was added into the culture medium of Vero cells before
simultaneously
or after the cells were infected with HSV-2. The effects of HD-5 against HSV-2 were analyzed by CCK-8 assay
and cytopathic effect (CPE) was observed at 72 h after HSV-2 infection. Meanwhile
the influence of serum concentration on the antiviral activity of HD-5 was also evaluated. Results No obvious cytotoxic effect of HD-5 was found in cultured Vero cells within the concentration of 100 μg/ml. At a fixed dose of 100 μg/ml
HD-5 showed significant protective effect on Vero cells against HSV-2 (P0.01)
when it was added before or simultaneously with HSV-2 infection. While
the protective effect was not observed when it was added in 2 h after HSV-2 infection (P0.05). The antiviral activity of HD-5 was markedly reduced as the concentration of serum in the medium was increased. Conclusion HD-5 has significant antiviral activity against HSV-2 in vitro
probably through reducing adherence and host cell invasion of the virus.
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