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10.3389/fimmu.2022.820131

http://scihub22266oqcxt.onion/10.3389/fimmu.2022.820131
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suck abstract from ncbi


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pmid35251001      Front+Immunol 2022 ; 13 (ä): 820131
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  • Simvastatin Downregulates the SARS-CoV-2-Induced Inflammatory Response and Impairs Viral Infection Through Disruption of Lipid Rafts #MMPMID35251001
  • Teixeira L; Temerozo JR; Pereira-Dutra FS; Ferreira AC; Mattos M; Goncalves BS; Sacramento CQ; Palhinha L; Cunha-Fernandes T; Dias SSG; Soares VC; Barreto EA; Cesar-Silva D; Fintelman-Rodrigues N; Pao CRR; de Freitas CS; Reis PA; Hottz ED; Bozza FA; Bou-Habib DC; Saraiva EM; de Almeida CJG; Viola JPB; Souza TML; Bozza PT
  • Front Immunol 2022[]; 13 (ä): 820131 PMID35251001show ga
  • Coronavirus disease 2019 (COVID-19) is currently a worldwide emergency caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). In observational clinical studies, statins have been identified as beneficial to hospitalized patients with COVID-19. However, experimental evidence of underlying statins protection against SARS-CoV-2 remains elusive. Here we reported for the first-time experimental evidence of the protective effects of simvastatin treatment both in vitro and in vivo. We found that treatment with simvastatin significantly reduced the viral replication and lung damage in vivo, delaying SARS-CoV-2-associated physiopathology and mortality in the K18-hACE2-transgenic mice model. Moreover, simvastatin also downregulated the inflammation triggered by SARS-CoV-2 infection in pulmonary tissue and in human neutrophils, peripheral blood monocytes, and lung epithelial Calu-3 cells in vitro, showing its potential to modulate the inflammatory response both at the site of infection and systemically. Additionally, we also observed that simvastatin affected the course of SARS-CoV-2 infection through displacing ACE2 on cell membrane lipid rafts. In conclusion, our results show that simvastatin exhibits early protective effects on SARS-CoV-2 infection by inhibiting virus cell entry and inflammatory cytokine production, through mechanisms at least in part dependent on lipid rafts disruption.
  • |*COVID-19 Drug Treatment[MESH]
  • |Animals[MESH]
  • |COVID-19/virology[MESH]
  • |Disease Models, Animal[MESH]
  • |Down-Regulation/*drug effects[MESH]
  • |Humans[MESH]
  • |Inflammation/*drug therapy/virology[MESH]
  • |Lung/virology[MESH]
  • |Membrane Microdomains/*drug effects[MESH]
  • |Mice[MESH]
  • |Mice, Transgenic[MESH]
  • |SARS-CoV-2/*pathogenicity[MESH]
  • |Simvastatin/*pharmacology[MESH]


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