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10.3389/fimmu.2020.574593

http://scihub22266oqcxt.onion/10.3389/fimmu.2020.574593
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33072117!7530822!33072117
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suck abstract from ncbi

pmid33072117      Front+Immunol 2020 ; 11 (?): 574593
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  • Familial Mediterranean Fever and COVID-19: Friends or Foes? #MMPMID33072117
  • Stella A; Lamkanfi M; Portincasa P
  • Front Immunol 2020[]; 11 (?): 574593 PMID33072117show ga
  • Familial Mediterranean Fever (FMF) and COVID-19 show a remarkable overlap of clinical symptoms and similar laboratory findings. Both are characterized by fever, abdominal/chest pain, elevation of C-reactive protein, and leukocytosis. In addition, colchicine and IL-1 inhibitors treatments that are effective in controlling inflammation in FMF patients have recently been proposed for off-label use in COVID-19 patients. Thus, FMF may resemble a milder recapitulation of the cytokine storm that is a hallmark of COVID-19 patients progressing to severe disease. We analyzed the sequence of the MEFV-encoded Pyrin protein - whose mutations cause FMF- in mammals, bats and pangolin. Intriguingly, although Pyrin is extremely conserved in species that are considered either a reservoir or intermediate hosts for SARS-CoV-2, some of the most common FMF-causing variants in humans are present as wildtype residues in these species. We propose that in humans, Pyrin may have evolved to fight highly pathogenic infections.
  • |*Betacoronavirus/genetics/immunology[MESH]
  • |*Coronavirus Infections/drug therapy/epidemiology/genetics/immunology[MESH]
  • |*Familial Mediterranean Fever/drug therapy/epidemiology/genetics/immunology[MESH]
  • |*Mutation[MESH]
  • |*Pandemics[MESH]
  • |*Pneumonia, Viral/drug therapy/epidemiology/genetics/immunology[MESH]
  • |*Pyrin/genetics/immunology[MESH]
  • |Animals[MESH]
  • |C-Reactive Protein/genetics/immunology[MESH]
  • |COVID-19[MESH]
  • |Colchicine/*therapeutic use[MESH]
  • |Humans[MESH]


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