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Projekt Druckansicht

SARS-CoV-2 induzierte Schädigung des Alveolarepithels und dessen Inhibition durch α1-antitrypsin.

Fachliche Zuordnung Anatomie und Physiologie
Virologie
Förderung Förderung von 2021 bis 2022
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 458685747
 
Erstellungsjahr 2022

Zusammenfassung der Projektergebnisse

The primary replication site of SARS-CoV-2 is the upper and lower respiratory tract. To identify antiviral factors that may restrict natural SARS-CoV-2 infection, we screened a protein library from derived from lung fluids and identified the protease inhibitor alpha -1 antitrypsin (α1-AT) as inhibitor of the new Coronavirus. We showed that α1-AT inhibits SARS-CoV-2 infection by blocking the function of the cellular protease TMPRRS2, which primes the viral Spike protein and the makes the virus infectious. Using primary airway epithelial cells as most relevant infection model, we also found that α1-AT prevents SARS-CoV-2 infection and replication. The antiviral activity of the α1-AT is not restricted to the original SARS-CoV-2 virus but also extends to all variants of concerns tested, including Omicron, and other TMPRSS2-depending viruses. Our findings have direct translational potential as α1-AT is an approved drug for the therapy of α1-AT deficiency. Several clinical trials have been initiated whether α1-AT has therapeutic potential in COVID-19 treatment. Applicant Münch is currently evaluating the prophylactic and therapeutic efficacy of nebulized α1-AT in a non-human-primate model of SARS-CoV-2. Thus, the findings of this project might result in novel treatment option of COVID-19 and perhaps other respiratory virus infections.

Projektbezogene Publikationen (Auswahl)

 
 

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