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The cholesterol metabolite 27-hydroxycholesterol inhibits SARS-CoV-2 and is markedly decreased in COVID-19 patients

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  • معلومة اضافية
    • Contributors:
      Marcello A.; Civra A.; Milan Bonotto R.; Nascimento Alves L.; Rajasekharan S.; Giacobone C.; Caccia C.; Cavalli R.; Adami M.; Brambilla P.; Lembo D.; Poli G.; Leoni V.
    • الموضوع:
      2020
    • Collection:
      Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
    • نبذة مختصرة :
      There is an urgent need to identify antivirals against the coronavirus SARS-CoV-2 in the current COVID-19 pandemic and to contain future similar emergencies early on. Specific side-chain cholesterol oxidation products of the oxysterols family have been shown to inhibit a large variety of both enveloped and non-enveloped human viral pathogens. Here we report on the in vitro inhibitory activity of the redox active oxysterol 27-hydroxycholesterol against SARS-CoV-2 and against one of the common cold agents HCoV-OC43 human coronavirus without significant cytotoxicity. Interestingly, physiological serum levels of 27-hydroxycholesterol in SARS-CoV-2 positive subjects were significantly decreased compared to the matched control group, reaching a marked 50% reduction in severe COVID-19 cases. Moreover, no correlation at all was observed between 24-hydroxycholesterol and 25-hydroxycholesterol serum levels and the severity of the disease. Opposite to that of 27-hydroxycholesterol was the behaviour of two recognized markers of redox imbalance, i.e. 7-ketocholesterol and 7β-hydroxycholesterol, whose serum levels were significantly increased especially in severe COVID-19. The exogenous administration of 27-hydroxycholesterol may represent in the near future a valid antiviral strategy in the worsening of diseases caused by present and emerging coronaviruses.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/32810737; info:eu-repo/semantics/altIdentifier/wos/WOS:000571097100002; volume:36; firstpage:101682; lastpage:101692; numberofpages:11; journal:REDOX BIOLOGY; http://hdl.handle.net/2318/1768423; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85089410425
    • الرقم المعرف:
      10.1016/j.redox.2020.101682
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.73610A81