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10.1016/j.mehy.2020.110242

http://scihub22266oqcxt.onion/10.1016/j.mehy.2020.110242
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suck abstract from ncbi


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pmid33254548      Med+Hypotheses 2020 ; 144 (ä): 110242
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  • Heme oxygenase-1 (HO-1) cytoprotective pathway: A potential treatment strategy against coronavirus disease 2019 (COVID-19)-induced cytokine storm syndrome #MMPMID33254548
  • Rossi M; Piagnerelli M; Van Meerhaeghe A; Zouaoui Boudjeltia K
  • Med Hypotheses 2020[Nov]; 144 (ä): 110242 PMID33254548show ga
  • The outbreak of coronavirus disease 2019 (COVID-19) requires urgent need for effective treatment. Severe COVID-19 is characterized by a cytokine storm syndrome with subsequent multiple organ failure (MOF) and acute respiratory distress syndrome (ARDS), which may lead to intensive care unit and increased risk of death. While awaiting a vaccine, targeting COVID-19-induced cytokine storm syndrome appears currently as the efficient strategy to reduce the mortality of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The stress-responsive enzyme, heme oxygenase-1 (HO-1) is largely known to protect against inflammatory response in animal models. HO-1 is induced by hemin, a well-tolerated molecule, used for decades in the treatment of acute intermittent porphyria. Experimental studies showed that hemin-induced HO-1 mitigates cytokine storm and lung injury in mouse models of sepsis and renal ischemia-reperfusion injury. Furthermore, HO-1 may also control numerous viral infections by inhibiting virus replication. In this context, we suggest the hypothesis that HO-1 cytoprotective pathway might be a promising target to control SARS-CoV-2 infection and mitigate COVID-19-induced cytokine storm and subsequent ARDS.
  • |*COVID-19 Drug Treatment[MESH]
  • |Animals[MESH]
  • |Anti-Inflammatory Agents/therapeutic use[MESH]
  • |Antibodies, Monoclonal, Humanized/therapeutic use[MESH]
  • |COVID-19 Vaccines[MESH]
  • |COVID-19/*metabolism[MESH]
  • |Critical Care[MESH]
  • |Cytokine Release Syndrome/*drug therapy/prevention & control[MESH]
  • |Cytokines/metabolism[MESH]
  • |Heme Oxygenase-1/*metabolism[MESH]
  • |Hemin/metabolism[MESH]
  • |Humans[MESH]
  • |Inflammation[MESH]
  • |Interleukin-6/metabolism[MESH]
  • |Models, Theoretical[MESH]
  • |Polymorphism, Genetic[MESH]


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