Effect of Novel Formulations using Lipophilic Epigallocatechin-3-Gallate against Influenza Virus Infection

D. Dickinson, Shannon Xayaraj, S. Dickinson, Xueling Shao, S. Hsu
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引用次数: 3

Abstract

Influenza virus infection is associated with high morbidity and mortality, and effective prophylactic and therapeutic methods to reduce infection outbreaks are lacking. Vaccination and current prevention/treatment approaches are not associated with a decline in morbidity or mortality, either globally or in the United States. Neither vaccination nor current anti-viral drugs prevent viral entry into the body and host cells, but rather target post-infection events in individuals. Hand washing and sanitizing do not prevent aerosol viral transmission, which accounts for the majority of influenza virus infections. Therefore, protection of the epithelia of the respiratory tract from viral entry is a significant gap in preventive strategies that needs to be filled. We hypothesize that lipophilic epigallocatechin3-gallate (L-EGCG), and EGCG-palmitate (EC16) in particular, is able to fill this gap and become a first-in-class prophylactic and therapeutic approach against influenza virus infection. The objective of the current study was to investigate a proof-of-concept for the use of EC16 to prevent and treat influenza virus infection. The experimental design included direct contact of formulations containing EC16 with H1N1 influenza virus prior to infection assay (TCID50) in MDCK cells, incubation of cells with EC16 formulations either before or after H1N1 viral infection (without direct formulation contact with the virus), and coating the cell surface with EC16 formulations prior to H1N1 viral infection, followed by TCID50 assays. The results demonstrated that at a 0.1% concentration, EC16 formulations were effective (>95%) in blocking H1N1 infection regardless of direct contact with the virus. In conclusion, formulations containing EC16 could be an effective prophylactic and therapeutic approach to combat influenza infection in the respiratory tract, pending further in vitro and in vivo studies.
亲脂性表没食子儿茶素-3-没食子酸酯新制剂抗流感病毒感染的作用
流感病毒感染与高发病率和死亡率有关,缺乏有效的预防和治疗方法来减少感染暴发。无论是在全球还是在美国,疫苗接种和目前的预防/治疗方法都与发病率或死亡率的下降无关。疫苗接种和目前的抗病毒药物都不能阻止病毒进入人体和宿主细胞,而是针对个体的感染后事件。洗手和消毒并不能防止气溶胶病毒传播,而气溶胶病毒是造成流感病毒感染的主要原因。因此,保护呼吸道上皮细胞免受病毒侵入是预防策略中的一个重要空白,需要填补。我们假设亲脂性没食子儿茶素-没食子酸酯(L-EGCG),特别是egcg -棕榈酸酯(EC16)能够填补这一空白,成为预防和治疗流感病毒感染的一流方法。当前研究的目的是调查使用EC16预防和治疗流感病毒感染的概念验证。实验设计包括:在MDCK细胞感染试验前,将含有EC16的制剂与H1N1流感病毒直接接触(TCID50);在H1N1病毒感染之前或之后,将含有EC16制剂的细胞孵化(制剂与病毒不直接接触);在H1N1病毒感染之前,在细胞表面涂覆EC16制剂,然后进行TCID50试验。结果表明,在0.1%的浓度下,EC16制剂在阻断H1N1感染方面是有效的(约95%),而与病毒没有直接接触。总之,含有EC16的配方可能是对抗呼吸道流感感染的有效预防和治疗方法,有待进一步的体外和体内研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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