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10.26355/eurrev_202007_22293

http://scihub22266oqcxt.onion/10.26355/eurrev_202007_22293
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32744716!ä!32744716

suck abstract from ncbi


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pmid32744716      Eur+Rev+Med+Pharmacol+Sci 2020 ; 24 (14): 7880-7885
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  • SARS-CoV-2 vs SARS-CoV-1 management: antibiotics and inflammasome modulators potential #MMPMID32744716
  • Rat P; Olivier E; Dutot M
  • Eur Rev Med Pharmacol Sci 2020[Jul]; 24 (14): 7880-7885 PMID32744716show ga
  • The coronavirus SARS-CoV-2 at the origin of COVID-19 shares more than 70% genetic similarity with SARS-CoV-1 that was at the origin of 2003 SARS. Infection-associated symptoms are very similar between SARS and COVID-19 diseases and are the same as community-acquired pneumonia symptoms. Antibiotics were empirically given to SARS patients in the early stages of the pathology whereas a different strategy has been decided in the management of COVID-19 pandemic with a worldwide shutdown. The cytokine storm, both identified in SARS and COVID-19 severe cases, is generated through inflammasome activation, which opens therapeutic perspectives to counteract the pathogenic inflammation. As corticoids have numerous side effects that limit their use, focusing on anti-inflammasome agents could represent a safer alternative for patients with severe COVID-19.
  • |Adrenal Cortex Hormones/therapeutic use[MESH]
  • |Anti-Bacterial Agents/*therapeutic use[MESH]
  • |Betacoronavirus/isolation & purification[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*drug therapy/epidemiology[MESH]
  • |Humans[MESH]
  • |Inflammasomes/chemistry/metabolism[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy/epidemiology[MESH]
  • |Purinergic P2X Receptor Antagonists/therapeutic use[MESH]
  • |Receptors, Purinergic P2X7/chemistry/metabolism[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe Acute Respiratory Syndrome/*drug therapy/epidemiology/virology[MESH]


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