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10.1136/jitc-2020-000930

http://scihub22266oqcxt.onion/10.1136/jitc-2020-000930
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32385146!7211108!32385146
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suck abstract from ncbi


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pmid32385146      J+Immunother+Cancer 2020 ; 8 (1): ä
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  • The Society for Immunotherapy of Cancer perspective on regulation of interleukin-6 signaling in COVID-19-related systemic inflammatory response #MMPMID32385146
  • Arnaldez FI; O'Day SJ; Drake CG; Fox BA; Fu B; Urba WJ; Montesarchio V; Weber JS; Wei H; Wigginton JM; Ascierto PA
  • J Immunother Cancer 2020[May]; 8 (1): ä PMID32385146show ga
  • The pandemic caused by the novel coronavirus SARS-CoV-2 has placed an unprecedented burden on healthcare systems around the world. In patients who experience severe disease, acute respiratory distress is often accompanied by a pathological immune reaction, sometimes referred to as 'cytokine storm'. One hallmark feature of the profound inflammatory state seen in patients with COVID-19 who succumb to pneumonia and hypoxia is marked elevation of serum cytokines, especially interferon gamma, tumor necrosis factor alpha, interleukin 17 (IL-17), interleukin 8 (IL-8) and interleukin 6 (IL-6). Initial experience from the outbreaks in Italy, China and the USA has anecdotally demonstrated improved outcomes for critically ill patients with COVID-19 with the administration of cytokine-modulatory therapies, especially anti-IL-6 agents. Although ongoing trials are investigating anti-IL-6 therapies, access to these therapies is a concern, especially as the numbers of cases worldwide continue to climb. An immunology-informed approach may help identify alternative agents to modulate the pathological inflammation seen in patients with COVID-19. Drawing on extensive experience administering these and other immune-modulating therapies, the Society for Immunotherapy of Cancer offers this perspective on potential alternatives to anti-IL-6 that may also warrant consideration for management of the systemic inflammatory response and pulmonary compromise that can be seen in patients with severe COVID-19.
  • |*Immunotherapy[MESH]
  • |*Societies, Medical[MESH]
  • |Adoptive Transfer[MESH]
  • |Antibodies, Monoclonal, Humanized/pharmacology/therapeutic use[MESH]
  • |Antibodies, Monoclonal/pharmacology/therapeutic use[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*complications/*drug therapy/immunology/pathology[MESH]
  • |Cytokine Release Syndrome/complications/drug therapy/immunology/pathology[MESH]
  • |Granulocyte-Macrophage Colony-Stimulating Factor/antagonists & inhibitors[MESH]
  • |Humans[MESH]
  • |Inflammation/complications/drug therapy/immunology/pathology[MESH]
  • |Interferon-gamma/antagonists & inhibitors[MESH]
  • |Interleukin-1/antagonists & inhibitors[MESH]
  • |Interleukin-17/antagonists & inhibitors[MESH]
  • |Interleukin-23/antagonists & inhibitors[MESH]
  • |Interleukin-6/*antagonists & inhibitors/genetics/*immunology/metabolism[MESH]
  • |Janus Kinases/antagonists & inhibitors[MESH]
  • |Neoplasms/immunology/therapy[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*complications/*drug therapy/immunology/pathology[MESH]
  • |Respiratory Distress Syndrome/*complications/*drug therapy/immunology/pathology[MESH]
  • |STAT Transcription Factors/antagonists & inhibitors[MESH]
  • |Severe Acute Respiratory Syndrome/pathology[MESH]
  • |Signal Transduction/drug effects[MESH]


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