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10.3389/fimmu.2020.01102

http://scihub22266oqcxt.onion/10.3389/fimmu.2020.01102
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32670273!7326128!32670273
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suck abstract from ncbi


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pmid32670273      Front+Immunol 2020 ; 11 (ä): 1102
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  • Battling COVID-19 Pandemic: Sphingosine-1-Phosphate Analogs as an Adjunctive Therapy? #MMPMID32670273
  • Naz F; Arish M
  • Front Immunol 2020[]; 11 (ä): 1102 PMID32670273show ga
  • With the sudden outbreak of COVID-19 patient worldwide and associated mortality, it is critical to come up with an effective treatment against SARS-CoV-2. Studies suggest that mortality due to COVID 19 is mainly attributed to the hyper inflammatory response leading to cytokine storm and ARDS in infected patients. Sphingosine-1-phosphate receptor 1 (S1PR1) analogs, AAL-R and RP-002, have earlier provided in-vivo protection from the pathophysiological response during H1N1 influenza infection and improved mortality. Recently, it was shown that the treatment with sphingosine-1-phosphate receptor 1 analog, CYM5442, resulted in the significant dampening of the immune response upon H1N1 challenge in mice and improved survival of H1N1 infected mice in combination with an antiviral drug, oseltamivir. Hence, here we suggest to investigate the possible utility of using S1P analogs to treat COVID-19.
  • |Animals[MESH]
  • |Betacoronavirus/drug effects/immunology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*drug therapy[MESH]
  • |Cytokine Release Syndrome/*prevention & control[MESH]
  • |Humans[MESH]
  • |Indans/*therapeutic use[MESH]
  • |Influenza A Virus, H1N1 Subtype/drug effects[MESH]
  • |Lysophospholipids/*agonists[MESH]
  • |Mice[MESH]
  • |Orthomyxoviridae Infections/drug therapy/prevention & control[MESH]
  • |Oseltamivir/therapeutic use[MESH]
  • |Oxadiazoles/*therapeutic use[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy[MESH]
  • |SARS-CoV-2[MESH]
  • |Sphingosine-1-Phosphate Receptors/*metabolism[MESH]


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