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COVID-19: Famotidine, Histamine, Mast Cells, and Mechanisms.
Malone, Robert W; Tisdall, Philip; Fremont-Smith, Philip; Liu, Yongfeng; Huang, Xi-Ping; White, Kris M; Miorin, Lisa; Moreno, Elena; Alon, Assaf; Delaforge, Elise; Hennecker, Christopher D; Wang, Guanyu; Pottel, Joshua; Blair, Robert V; Roy, Chad J; Smith, Nora; Hall, Julie M; Tomera, Kevin M; Shapiro, Gideon; Mittermaier, Anthony; Kruse, Andrew C; García-Sastre, Adolfo; Roth, Bryan L; Glasspool-Malone, Jill; Ricke, Darrell O.
  • Malone RW; RW Malone MD LLC, Madison, VA, United States.
  • Tisdall P; Icahn School of Medicine at Mount Sinai, The Tisch Cancer Institute, New York, NY, United States.
  • Fremont-Smith P; Medical School Companion LLC, Marco Island, FL, United States.
  • Liu Y; MIT Lincoln Laboratory, Lexington, MA, United States.
  • Huang XP; Department of Pharmacology, University of North Carolina, Chapel Hill, Chapel Hill, NC, United States.
  • White KM; Department of Pharmacology, University of North Carolina, Chapel Hill, Chapel Hill, NC, United States.
  • Miorin L; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Moreno E; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Alon A; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Delaforge E; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Hennecker CD; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Wang G; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Pottel J; Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Boston, MA, United States.
  • Blair RV; Department of Chemistry, McGill University, Montreal, QC, Canada.
  • Roy CJ; Department of Chemistry, McGill University, Montreal, QC, Canada.
  • Smith N; Department of Chemistry, McGill University, Montreal, QC, Canada.
  • Hall JM; Molecular Forecaster Inc, Montreal, QC, Canada.
  • Tomera KM; Tulane National Primate Research Center, Covington, LA, United Sates.
  • Shapiro G; Department of Pathology and Laboratory Animal Medicine, Tulane University School of Medicine, New Orleans, LA, United States.
  • Mittermaier A; Tulane National Primate Research Center, Covington, LA, United Sates.
  • Kruse AC; Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, LA, United States.
  • García-Sastre A; MIT Lincoln Laboratory, Lexington, MA, United States.
  • Roth BL; Frank H. Netter MD School of Medicine - Quinnipiac University, Hamden, CT, United States.
  • Glasspool-Malone J; Department of Urology, Beloit Memorial Hospital, Beloit, WI, United States.
  • Ricke DO; Pharmorx LLC, Gainesville, FL, United States.
Front Pharmacol ; 12: 633680, 2021.
Article in English | MEDLINE | ID: covidwho-1175552
ABSTRACT
SARS-CoV-2 infection is required for COVID-19, but many signs and symptoms of COVID-19 differ from common acute viral diseases. SARS-CoV-2 infection is necessary but not sufficient for development of clinical COVID-19 disease. Currently, there are no approved pre- or post-exposure prophylactic COVID-19 medical countermeasures. Clinical data suggest that famotidine may mitigate COVID-19 disease, but both mechanism of action and rationale for dose selection remain obscure. We have investigated several plausible hypotheses for famotidine activity including antiviral and host-mediated mechanisms of action. We propose that the principal mechanism of action of famotidine for relieving COVID-19 symptoms involves on-target histamine receptor H2 activity, and that development of clinical COVID-19 involves dysfunctional mast cell activation and histamine release. Based on these findings and associated hypothesis, new COVID-19 multi-drug treatment strategies based on repurposing well-characterized drugs are being developed and clinically tested, and many of these drugs are available worldwide in inexpensive generic oral forms suitable for both outpatient and inpatient treatment of COVID-19 disease.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Language: English Journal: Front Pharmacol Year: 2021 Document Type: Article Affiliation country: Fphar.2021.633680

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Language: English Journal: Front Pharmacol Year: 2021 Document Type: Article Affiliation country: Fphar.2021.633680