水溶性蜂胶(Greit 120)与人α干扰素(HuIFN-αN3)体外抗流感病毒的加性作用

Filipič Bratko, Gradišnik Lidija, Pereyra Adriana, Kopinč Rok, Rihar Klemen, Ružić-Sabljić Eva, K. Snežana, Đermić Damir, Šooš Eugen, Volpi Nicola, F. Alfredo, H. Mazija
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引用次数: 0

摘要

流感病毒影响人类呼吸道,引起一系列明显的症状,包括发烧、鼻分泌物、咳嗽、头痛、肌肉疼痛和肺炎,这些症状可能变得剧烈和严重。发现甲型流感病毒对金刚烷胺和金刚乙胺仍然具有耐药性,对奥司他韦具有高度耐药性。因此,有必要不断改进对耐药流感病毒有效的药物。蜂胶在体内和体外均具有抗流感活性。人白细胞干扰素(HuIFN-α n3)是一种对流感病毒具有抗病毒活性的多亚型蛋白。本实验研究了水溶性蜂胶(WSP) (Greit 120)与惠氏蛋白-αN3以不同比例混合后的抗流感活性。采用HPLC-UV-ESI- MS504971和反相高效液相色谱(RP-HPLC)对Greit 120多酚、总酚酸和生物类黄酮进行了表征。分别用WSP (Greit 120)和HuIFN-αN3单独或按1:1、1:2和2:1的比例添加甲型流感病毒和乙型流感病毒到lc - mk2细胞中。培养皿孵育,测定细胞病变效应。10% WSP与HuIFN-αN3按1:2的比例混合,对甲型流感病毒和乙型流感病毒的ID50分别为12±0.2 μg/mL和19±0.6 μg/mL。比较WSP (Greit 120)/HuIFN-α n3与利巴韦林的抗流感活性,发现WSP (Greit 120)/HuIFN-α n3的最佳配比为1:2(甲型流感0.5,乙型流感0.6)。该新配方的WSP (Greit 120)和HuIFN-αN3具有较好的抗流感活性,必将提高其在流感感染中的应用。
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Additive Effects of Water-Soluble Propolis (Greit 120) and Human Interferon Alfa (HuIFN-αN3) against Influenza Viruses in Vitro
Influenza virus affects the respiratory tract in humans causing a range of distinct manifestations including fever, nasal secretions, cough, headaches, muscle pain and pneumonia, which could become violent and severe. It was found that influenza A viruses remain resistant to amantadine and rimantadin with high level of oseltamvir resistance. Therefore, there is a need for constant improvement of drugs active against resistant influenza viruses. Propolis has anti-influenza activity both in vitro and in vivo. Human leukocyte interferon (HuIFN-αN3) is a multi- subtype protein that displays an antiviral activity against influenza virus. In this study we elucidated the anti-influenza activity of the mixes of water-soluble propolis (WSP) (Greit 120) and HuIFN-αN3 at different ratios. Greit 120 polyphenols, total phenol acids and bioflavonoid were characterized by HPLC-UV-ESI- MS504971 and HuIFN-αN3 by reverse-phase high- performance liquid chromatography (RP-HPLC). Influenza A and B viruses were separately added to the LLC-MK2 cells treated with WSP (Greit 120) and HuIFN-αN3 alone or in proportions 1:1, 1:2 and 2:1. Plates were incubated and cytopathic effect was determined. The best results (ID50) were obtained with the mix of 10% WSP and HuIFN-αN3 in proportion 1:2, showing ID50 at 12 ± 0.2 μg/mL and 19 ± 0.6 μg/mL for influenza A and B viruses, respectively. When comparing anti- influenza activity of WSP (Greit 120)/HuIFN-αN3 with that of ribavirin, it was found that 1:2 was the optimal ratio for WSP (Greit 120)/HuIFN-αN3 (0.5 and 0.6 for influenza A and B, respectively). This new formulation of WSP (Greit 120) and HuIFN-αN3, showing better anti-Influenza activity, will definitely improve its application in flu infections.
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