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罂粟碱靶向 STAT 信号通路:一种针对 SARS-CoV-2 的双重作用治疗选择。

Papaverine Targets STAT Signaling: A Dual-Action Therapy Option Against SARS-CoV-2.

作者信息

Reus Philipp, Torbica Emma, Rothenburger Tamara, Bechtel Marco, Kandler Joshua, Ciesek Sandra, Gribbon Philip, Kannt Aimo, Cinatl Jindrich, Bojkova Denisa

机构信息

Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, ScreeningPort, Hamburg, Germany.

Institute for Medical Virology, University Hospital, Goethe University Frankfurt, Frankfurt, Germany.

出版信息

J Med Virol. 2025 Apr;97(4):e70319. doi: 10.1002/jmv.70319.

Abstract

Papaverine (PV) has been previously identified as a promising candidate in SARS-CoV-2 repurposing screens. In this study, we further investigated both its antiviral and immunomodulatory properties. PV displayed antiviral efficacy against SARS-CoV-2 and influenza A viruses H1N1 and H5N1 in single infection as well as in co-infection. We demonstrated PV's activity against various SARS-CoV-2 variants and identified its action at the post-entry stage of the viral life cycle. Notably, treatment of air-liquid interface (ALI) cultures of primary bronchial epithelial cells with PV significantly inhibited SARS-CoV-2 levels. Additionally, PV was found to attenuate interferon (IFN) signaling independently of viral infection. Mechanistically, PV decreased the activation of the IFN-stimulated response element following stimulation with all three IFN types by suppressing STAT1 and STAT2 phosphorylation and nuclear translocation. Furthermore, the combination of PV with approved COVID-19 therapeutics molnupiravir and remdesivir demonstrated synergistic effects. Given its immunomodulatory effects and clinical availability, PV shows promising potential as a component for combination therapy against COVID-19.

摘要

罂粟碱(PV)此前已被确定为在新冠病毒(SARS-CoV-2)药物再利用筛选中颇具潜力的候选药物。在本研究中,我们进一步探究了其抗病毒和免疫调节特性。PV在单一感染以及共同感染中均显示出对SARS-CoV-2、甲型流感病毒H1N1和H5N1的抗病毒功效。我们证明了PV对多种SARS-CoV-2变体的活性,并确定了其在病毒生命周期进入后阶段的作用。值得注意的是,用PV处理原代支气管上皮细胞的气液界面(ALI)培养物可显著抑制SARS-CoV-2水平。此外,发现PV可独立于病毒感染减弱干扰素(IFN)信号传导。从机制上讲,PV通过抑制STAT1和STAT2的磷酸化及核转位,降低了在用所有三种IFN类型刺激后干扰素刺激反应元件的激活。此外,PV与已获批的新冠治疗药物莫努匹韦和瑞德西韦联合使用显示出协同效应。鉴于其免疫调节作用和临床可用性,PV作为抗新冠联合治疗的一种成分显示出有前景的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/475b/11963225/da3cb4b26898/JMV-97-e70319-g005.jpg

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