表没食子儿茶素-3-没食子酸酯(EGCG)抑制灵长类动物上皮细胞感染SARS-CoV-2:(简短通讯)

B. Hurst, D. Dickinson, S. Hsu
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引用次数: 9

摘要

截至2020年1月30日,导致COVID-19大流行的新型冠状病毒SARS-CoV-2在美国造成了1.26亿例病例,4.37万例死亡。到那时为止,全球已有1.02亿例感染病例,死亡人数攀升至221万。在英国、巴西和南非出现的SARS-CoV-2突变变体与更高的传播率和相关的死亡有关。因此,迫切需要新的治疗和预防SARS-CoV-2方法。虽然一些抗病毒药物,如Remdesivir,可以缓解某些患者群体,但其他现有的抗病毒药物或FDA批准的药物组合尚未显示出对COVID-19的临床疗效。具有强大而广泛的抗病毒特性,对呼吸道病毒具有不同作用机制的化合物可能为对抗SARS-CoV-2及其变体提供新方法,特别是如果这些化合物被归类为一般公认的安全化合物(GRAS)。大量证据表明,表没食子儿茶素-3-没食子酸酯(EGCG)及其衍生物作为抗多种致病性病毒感染的有效药物具有良好的潜力。然而,EGCG或其衍生物尚未直接针对SARS-CoV-2进行测试。本研究旨在评估EGCG在灵长类动物上皮细胞中对SARS-CoV-2感染的潜在抗病毒活性。本研究采用的方法包括细胞病变效应(CPE)试验和病毒产量降低(VYR)试验,分别使用Vero 76(绿猴上皮细胞)和Caco-2(人上皮细胞)细胞系。结果表明,EGCG浓度为0.27 μg/ml (0.59 μM)时,对Vero 76细胞的SARS-CoV-2感染抑制率为50%(即EC50=0.27 μg/ml)。EGCG在EC90=28 μg/ml (61 μM)时也能抑制Caco-2细胞的SARS-CoV-2感染。据我们所知,这些结果是首次观察到EGCG对SARS-CoV-2的抗病毒活性,并表明EGCG及其衍生物可用于对抗COVID-19和其他呼吸道病毒感染引起的疾病,有待于体内和临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epigallocatechin-3-Gallate (EGCG) Inhibits SARS-CoV-2 Infection in Primate Epithelial Cells: (A Short Communication).
SARS-CoV-2, the novel coronavirus responsible for the COVID-19 pandemic, caused >26 million cases in the United States and >437,000 deaths as of Jan 30, 2020. Worldwide by that date, there had been 102 million cases of infections, and deaths had climbed to 2.21 million. Mutated variants of SARS-CoV-2 that have emerged from the United Kingdom, Brazil, and South Africa are associated with higher transmission rates and associated deaths. Therefore, novel therapeutic and prophylactic methods against SARS-CoV-2 are in urgent need. While some antiviral drugs, such as Remdesivir, provide relief to certain patient populations, other existing antiviral drugs or combinations of FDA approved pharmaceuticals have yet to show clinical efficacy against COVID-19. Compounds that possess strong and broad antiviral properties with different mechanisms of action against respiratory viruses may provide novel approaches to combat SARS-CoV-2 and its variants, especially if the compounds are classified as generally recognized as safe (GRAS). A large body of evidence indicates a promising potential for the use of epigallocatechin-3-gallate (EGCG) and its derivatives as effective agents against infections from a wide range of pathogenic viruses. However, EGCG or its derivatives have not been tested directly against SARS-CoV-2. The current study was designed to evaluate the potential antiviral activity of EGCG against SARS-CoV-2 infection in primate epithelial cells. Methods applied in the study include cytopathic effect (CPE) assay and virus yield reduction (VYR) assays using Vero 76 (green monkey epithelial cells) and Caco-2 (human epithelial cells) cell lines, respectively. The results demonstrated that EGCG at 0.27 μg/ml (0.59 μM) inhibited SARS-CoV-2 infection in Vero 76 cells by 50% (i.e., EC50=0.27 μg/ml). EGCG also inhibited SARS-CoV-2 infection in Caco-2 cells with EC90=28 μg/ml (61 μM). These results, to the best of our knowledge, are the first observations on the antiviral activities of EGCG against SARS-CoV-2, and suggest that EGCG and its derivatives could be used to combat COVID-19 and other respiratory viral infection-induced illness, pending in vivo and clinical studies.
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