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深入探究地塞米松与SARS-CoV-2引发的细胞因子风暴:对首款挽救生命的COVID-19药物的计算机模拟见解

A Closer Look at Dexamethasone and the SARS-CoV-2-Induced Cytokine Storm: In Silico Insights of the First Life-Saving COVID-19 Drug.

作者信息

Morgan Paul, Arnold Shareen J, Hsiao Nai-Wan, Shu Chih-Wen

机构信息

Faculty of Science and Technology, University of Belize, Belmopan 501, Belize.

Department of Biology, National Changhua University of Education, Changhua 50007, Taiwan.

出版信息

Antibiotics (Basel). 2021 Dec 8;10(12):1507. doi: 10.3390/antibiotics10121507.

Abstract

The term cytokine storm refers to an uncontrolled overproduction of soluble inflammatory markers known as cytokines and chemokines. Autoimmune destruction of the lungs triggered by the release of these inflammatory markers often induces acute respiratory distress syndrome (ARDS). ARDS is an emergency condition with a high mortality rate in COVID-19 patients. Dexamethasone is the first repurposed corticosteroid with life-saving efficacy in patients with severe SARS-CoV-2 infection. Dexamethasone has traditionally been known to suppress the production of inflammatory markers at the transcriptional level, but its role as a direct therapeutic to neutralize cytokines, chemokines, their receptors, and functionally critical SARS-CoV-2 proteins has not yet been explored. Herein, we demonstrated that dexamethasone binds with high affinity to interlukin-1 (IL-1), IL-6, IL-8, IL-12, IL-21, INF2, TGFβ-1, INF-γ, CXCL8, some of the receptors, IL-1R, IL-21R, IFNGR, INFAR, IL-6αR-gp130, ST2 and the SARS-CoV-2 protein NSP macro X, and 3CLpro, forming stable drug-protein complexes. Our work implied that dexamethasone has the potential to directly neutralize inflammatory markers, further supporting its life-saving potential in patients with severe manifestations of COVID-19.

摘要

细胞因子风暴一词指的是可溶性炎症标志物(即细胞因子和趋化因子)不受控制地过度产生。这些炎症标志物的释放引发的肺部自身免疫性破坏通常会诱发急性呼吸窘迫综合征(ARDS)。ARDS是一种紧急情况,在新冠病毒疾病(COVID-19)患者中死亡率很高。地塞米松是第一种被重新用于治疗严重SARS-CoV-2感染患者且具有挽救生命功效的皮质类固醇。传统上已知地塞米松在转录水平抑制炎症标志物的产生,但其作为直接中和细胞因子、趋化因子、它们的受体以及功能关键的SARS-CoV-2蛋白的治疗作用尚未得到探索。在此,我们证明地塞米松与白细胞介素-1(IL-1)、IL-6、IL-8、IL-12、IL-21、INF2、转化生长因子β-1(TGFβ-1)、干扰素-γ(INF-γ)、CXC趋化因子配体8(CXCL8)、一些受体(IL-1R、IL-21R、IFNGR、INFAR、IL-6αR-gp130、ST2)以及SARS-CoV-2蛋白NSP宏X和3C样蛋白酶(3CLpro)具有高亲和力结合,形成稳定的药物-蛋白质复合物。我们的工作表明地塞米松有可能直接中和炎症标志物,进一步支持其在COVID-19严重表现患者中的挽救生命潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2933/8698520/325dcb6031bf/antibiotics-10-01507-g001.jpg

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