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A proprietary topical preparation containing EGCG-stearate and glycerin with inhibitory effects on herpes simplex virus: case study.
Inflamm Allergy Drug Targets. 2012 Oct;11(5):364-8. doi: 10.2174/187152812803251033.
2
Efficacy results of a trial of a herpes simplex vaccine.一项单纯疱疹疫苗试验的疗效结果。
N Engl J Med. 2012 Jan 5;366(1):34-43. doi: 10.1056/NEJMoa1103151.
3
The green tea polyphenol, epigallocatechin-3-gallate, inhibits hepatitis C virus entry.绿茶多酚表没食子儿茶素没食子酸酯抑制丙型肝炎病毒进入。
Hepatology. 2011 Dec;54(6):1947-55. doi: 10.1002/hep.24610.
4
Epigallocatechin gallate inhibits HBV DNA synthesis in a viral replication - inducible cell line.没食子酸表没食子儿茶素酯可抑制病毒复制诱导细胞系中的 HBV DNA 合成。
World J Gastroenterol. 2011 Mar 21;17(11):1507-14. doi: 10.3748/wjg.v17.i11.1507.
5
Resistance of herpes simplex viruses to nucleoside analogues: mechanisms, prevalence, and management.单纯疱疹病毒对核苷类似物的耐药性:机制、流行率和管理。
Antimicrob Agents Chemother. 2011 Feb;55(2):459-72. doi: 10.1128/AAC.00615-10. Epub 2010 Nov 15.
6
Egress of HSV-1 capsid requires the interaction of VP26 and a cellular tetraspanin membrane protein.单纯疱疹病毒 1 衣壳的出芽需要 VP26 与一种细胞四跨膜蛋白的相互作用。
Virol J. 2010 Jul 14;7:156. doi: 10.1186/1743-422X-7-156.
7
Viral entry mechanisms: cellular and viral mediators of herpes simplex virus entry.病毒进入机制:单纯疱疹病毒进入的细胞和病毒介质。
FEBS J. 2009 Dec;276(24):7228-36. doi: 10.1111/j.1742-4658.2009.07402.x.
8
Antiviral effect of epigallocatechin gallate on enterovirus 71.表没食子儿茶素没食子酸酯对肠道病毒71型的抗病毒作用。
J Agric Food Chem. 2009 Jul 22;57(14):6140-7. doi: 10.1021/jf901128u.
9
The main green tea polyphenol epigallocatechin-3-gallate counteracts semen-mediated enhancement of HIV infection.主要的绿茶多酚表没食子儿茶素-3-没食子酸酯可抵消精液介导的HIV感染增强作用。
Proc Natl Acad Sci U S A. 2009 Jun 2;106(22):9033-8. doi: 10.1073/pnas.0811827106. Epub 2009 May 18.
10
Multiple peptides homologous to herpes simplex virus type 1 glycoprotein B inhibit viral infection.多种与1型单纯疱疹病毒糖蛋白B同源的肽可抑制病毒感染。
Antimicrob Agents Chemother. 2009 Mar;53(3):987-96. doi: 10.1128/AAC.00793-08. Epub 2008 Dec 22.

用改性绿茶多酚棕榈酰表没食子儿茶素没食子酸酯抑制单纯疱疹病毒 1 型。

Inhibition of herpes simplex virus type 1 with the modified green tea polyphenol palmitoyl-epigallocatechin gallate.

机构信息

Department of Biological Science, Seton Hall University, South Orange, NJ 07079, USA.

出版信息

Food Chem Toxicol. 2013 Feb;52:207-15. doi: 10.1016/j.fct.2012.11.006. Epub 2012 Nov 23.

DOI:10.1016/j.fct.2012.11.006
PMID:23182741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3703635/
Abstract

Green tea polyphenol epigallocatechin gallate (EGCG) is a strong antioxidant that has previously been shown to reduce the number of plaques in HIV-infected cultured cells. Modified EGCG, palmitoyl-EGCG (p-EGCG), is of interest as a topical antiviral agent for herpes simplex virus (HSV-1) infections. This study evaluated the effect of p-EGCG on HSV-infected Vero cells. Results of cell viability and cell proliferation assays indicate that p-EGCG is not toxic to cultured Vero cells and show that modification of the green tea polyphenol epigallocatechin gallate (EGCG) with palmitate increases the effectiveness of EGCG as an antiviral agent. Furthermore, p-EGCG is a more potent inhibitor of herpes simplex virus 1 (HSV-1) than EGCG and can be topically applied to skin, one of the primary tissues infected by HSV. Viral binding assay, plaque forming assay, PCR, real-time PCR, and fluorescence microscopy were used to demonstrate that p-EGCG concentrations of 50 μM and higher block the production of infectious HSV-1 particles. p-EGCG was found to inhibit HSV-1 adsorption to Vero cells. Thus, p-EGCG may provide a novel treatment for HSV-1 infections.

摘要

绿茶多酚表没食子儿茶素没食子酸酯(EGCG)是一种很强的抗氧化剂,先前已被证明可减少感染 HIV 的培养细胞中的斑块数量。棕榈酰化 EGCG(p-EGCG)是一种有前途的单纯疱疹病毒(HSV-1)感染的局部抗病毒药物。本研究评估了 p-EGCG 对感染 HSV 的vero 细胞的影响。细胞活力和细胞增殖试验的结果表明,p-EGCG 对培养的 vero 细胞没有毒性,并表明用棕榈酸修饰绿茶多酚表没食子儿茶素没食子酸酯(EGCG)增加了 EGCG 作为抗病毒剂的有效性。此外,p-EGCG 是一种比 EGCG 更有效的单纯疱疹病毒 1(HSV-1)抑制剂,可局部应用于皮肤,这是 HSV 感染的主要组织之一。病毒结合试验、空斑形成试验、PCR、实时 PCR 和荧光显微镜用于证明 50 μM 及更高浓度的 p-EGCG 可阻断感染性 HSV-1 颗粒的产生。发现 p-EGCG 可抑制 HSV-1 吸附到 vero 细胞。因此,p-EGCG 可能为 HSV-1 感染提供一种新的治疗方法。