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10.1177/1753466620933508

http://scihub22266oqcxt.onion/10.1177/1753466620933508
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32539627!7298425!32539627
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suck abstract from ncbi


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pmid32539627      Ther+Adv+Respir+Dis 2020 ; 14 (ä): 1753466620933508
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  • Lung under attack by COVID-19-induced cytokine storm: pathogenic mechanisms and therapeutic implications #MMPMID32539627
  • Pelaia C; Tinello C; Vatrella A; De Sarro G; Pelaia G
  • Ther Adv Respir Dis 2020[Jan]; 14 (ä): 1753466620933508 PMID32539627show ga
  • The lung is a key target of the cytokine storm that can be triggered by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), responsible for the widespread clinical syndrome known as coronavirus disease 2019 (COVID-19). Indeed, in some patients, SARS-CoV-2 promotes a dysfunctional immune response that dysregulates the cytokine secretory pattern. Hypercytokinemia underlies the hyperinflammatory state leading to injury of alveolar epithelial cells and vascular endothelial cells, as well as to lung infiltration sustained by neutrophils and macrophages. Within such a pathogenic context, interleukin-6 (IL-6) and other cytokines/chemokines play a pivotal pro-inflammatory role. Therefore, cytokines and their receptors, as well as cytokine-dependent intracellular signalling pathways can be targeted by potential therapies aimed to relieve the heavy burden of cytokine storm. In particular, the anti-IL-6-receptor monoclonal antibody tocilizumab is emerging as one of the most promising pharmacologic treatments. The reviews of this paper are available via the supplemental material section.
  • |*Betacoronavirus[MESH]
  • |*Immunity, Innate[MESH]
  • |Antibodies, Monoclonal, Humanized/*therapeutic use[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/drug therapy/*immunology/metabolism[MESH]
  • |Cytokines/*immunology/metabolism[MESH]
  • |Endothelial Cells/metabolism[MESH]
  • |Humans[MESH]
  • |Lung/*metabolism[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/drug therapy/*immunology/metabolism[MESH]


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