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EGCG,一种绿茶儿茶素,作为一种有潜力的治疗药物用于有症状和无症状的 SARS-CoV-2 感染。

EGCG, a Green Tea Catechin, as a Potential Therapeutic Agent for Symptomatic and Asymptomatic SARS-CoV-2 Infection.

机构信息

Center for Computational Biology and Bioinformatics, Amity Institute of Biotechnology, Amity University, Noida, Uttar Pradesh 201313, India.

Regeneron Pharmaceuticals Inc., Tarrytown, NY 10591, USA.

出版信息

Molecules. 2021 Feb 24;26(5):1200. doi: 10.3390/molecules26051200.

DOI:10.3390/molecules26051200
PMID:33668085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7956763/
Abstract

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has emerged to be the greatest threat to humanity in the modern world and has claimed nearly 2.2 million lives worldwide. The United States alone accounts for more than one fourth of 100 million COVID-19 cases across the globe. Although vaccination against SARS-CoV-2 has begun, its efficacy in preventing a new or repeat COVID-19 infection in immunized individuals is yet to be determined. Calls for repurposing of existing, approved, drugs that target the inflammatory condition in COVID-19 are growing. Our initial gene ontology analysis predicts a similarity between SARS-CoV-2 induced inflammatory and immune dysregulation and the pathophysiology of rheumatoid arthritis. Interestingly, many of the drugs related to rheumatoid arthritis have been found to be lifesaving and contribute to lower COVID-19 morbidity. We also performed in silico investigation of binding of epigallocatechin gallate (EGCG), a well-known catechin, and other catechins on viral proteins and identified papain-like protease protein (PLPro) as a binding partner. Catechins bind to the S1 ubiquitin-binding site of PLPro, which might inhibit its protease function and abrogate SARS-CoV-2 inhibitory function on ubiquitin proteasome system and interferon stimulated gene system. In the realms of addressing inflammation and how to effectively target SARS-CoV-2 mediated respiratory distress syndrome, we review in this article the available knowledge on the strategic placement of EGCG in curbing inflammatory signals and how it may serve as a broad spectrum therapeutic in asymptomatic and symptomatic COVID-19 patients.

摘要

新型冠状病毒病 2019(COVID-19),由严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)引起,已成为现代世界对人类的最大威胁,已导致全球近 220 万人死亡。仅美国就占全球 1 亿例 COVID-19 病例的四分之一以上。尽管已开始针对 SARS-CoV-2 进行疫苗接种,但在免疫个体中预防新的或重复 COVID-19 感染的功效尚未确定。人们越来越呼吁重新利用针对 COVID-19 炎症状态的现有、已批准的药物。我们的初始基因本体论分析预测,SARS-CoV-2 诱导的炎症和免疫失调与类风湿关节炎的病理生理学之间存在相似性。有趣的是,许多与类风湿关节炎相关的药物已被发现具有救生作用,并有助于降低 COVID-19 的发病率。我们还对表没食子儿茶素没食子酸酯(EGCG)和其他儿茶素与病毒蛋白的结合进行了计算机模拟研究,并确定木瓜蛋白酶样蛋白酶蛋白(PLPro)为结合伴侣。儿茶素结合到 PLPro 的 S1 泛素结合位点,这可能抑制其蛋白酶功能,并消除 SARS-CoV-2 对泛素蛋白酶体系统和干扰素刺激基因系统的抑制作用。在解决炎症和如何有效针对 SARS-CoV-2 介导的呼吸窘迫综合征的问题上,本文回顾了 EGCG 在抑制炎症信号方面的现有知识,以及它如何作为无症状和有症状 COVID-19 患者的广谱治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/72142d56eab6/molecules-26-01200-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/0498b04e839a/molecules-26-01200-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/81c083f3c087/molecules-26-01200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/72142d56eab6/molecules-26-01200-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/0498b04e839a/molecules-26-01200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/b350ea13188a/molecules-26-01200-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/0019dc9b2ce8/molecules-26-01200-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/81c083f3c087/molecules-26-01200-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4260/7956763/72142d56eab6/molecules-26-01200-g005.jpg

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