Abstract |
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.
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Authors | Alessandro Stella, Mohamed Lamkanfi, Piero Portincasa |
Journal | Frontiers in immunology
(Front Immunol)
Vol. 11
Pg. 574593
( 2020)
ISSN: 1664-3224 [Electronic] Switzerland |
PMID | 33072117
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2020 Stella, Lamkanfi and Portincasa. |
Chemical References |
- MEFV protein, human
- Pyrin
- C-Reactive Protein
- Colchicine
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Topics |
- Animals
- Betacoronavirus
(genetics, immunology)
- C-Reactive Protein
(genetics, immunology)
- COVID-19
- Colchicine
(therapeutic use)
- Coronavirus Infections
(drug therapy, epidemiology, genetics, immunology)
- Familial Mediterranean Fever
(drug therapy, epidemiology, genetics, immunology)
- Humans
- Mutation
- Pandemics
- Pneumonia, Viral
(drug therapy, epidemiology, genetics, immunology)
- Pyrin
(genetics, immunology)
- SARS-CoV-2
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