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10.3389/fimmu.2020.01714

http://scihub22266oqcxt.onion/10.3389/fimmu.2020.01714
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32793244!7385229!32793244
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suck abstract from ncbi


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pmid32793244      Front+Immunol 2020 ; 11 (ä): 1714
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  • COVID-19: Underlying Adipokine Storm and Angiotensin 1-7 Umbrella #MMPMID32793244
  • Mery G; Epaulard O; Borel AL; Toussaint B; Le Gouellec A
  • Front Immunol 2020[]; 11 (ä): 1714 PMID32793244show ga
  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the third coronavirus leading to a global health outbreak. Despite the high mortality rates from SARS-CoV-1 and Middle-East respiratory syndrome (MERS)-CoV infections, which both sparked the interest of the scientific community, the underlying physiopathology of the SARS-CoV-2 infection, remains partially unclear. SARS-CoV-2 shares similar features with SARS-CoV-1, notably the use of the angiotensin conversion enzyme 2 (ACE2) as a receptor to enter the host cells. However, some features of the SARS-CoV-2 pandemic are unique. In this work, we focus on the association between obesity, metabolic syndrome, and type 2 diabetes on the one hand, and the severity of COVID-19 infection on the other, as it seems greater in these patients. We discuss how adipocyte dysfunction leads to a specific immune environment that predisposes obese patients to respiratory failure during COVID-19. We also hypothesize that an ACE2-cleaved protein, angiotensin 1-7, has a beneficial action on immune deregulation and that its low expression during the SARS-CoV-2 infection could explain the severity of infection. This introduces angiotensin 1-7 as a potential candidate of interest in therapeutic research on CoV infections.
  • |Adipokines/blood/*immunology[MESH]
  • |Angiotensin I/*immunology[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Betacoronavirus/*immunology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*pathology[MESH]
  • |Diabetes Mellitus, Type 2/immunology[MESH]
  • |Humans[MESH]
  • |Metabolic Syndrome/immunology[MESH]
  • |Obesity/immunology[MESH]
  • |Pandemics[MESH]
  • |Peptide Fragments/*immunology[MESH]
  • |Peptidyl-Dipeptidase A/metabolism[MESH]
  • |Pneumonia, Viral/*pathology[MESH]
  • |SARS-CoV-2[MESH]


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