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Bacteriophage-Derived Double-Stranded RNA Exerts Anti-SARS-CoV-2 Activity In Vitro and in Golden Syrian Hamsters In
Kristine Vaivode1, Irina Verhovcova1, Dace Skrastina1
1Latvian Biomedical Research and Study Centre, Ratsrtupites Street 1, k-1, LV-1067 Riga, Latvia.
Pharmaceuticals (Basel, Switzerland)
|September 23, 2022
Summary
Larifan, a broad-spectrum antiviral medication, effectively inhibited SARS-CoV-2 replication in laboratory settings and in hamster models. This suggests Larifan
Area of Science:
- Virology
- Immunology
- Pharmacology
Background:
- Bacteriophage-derived double-stranded RNA (dsRNA) is a known broad-spectrum antiviral agent.
- Larifan is a well-established antiviral medication in national use.
- The emergence of SARS-CoV-2 necessitates the evaluation of existing antiviral therapies.
Purpose of the Study:
- To investigate the antiviral efficacy of Larifan against SARS-CoV-2.
- To assess Larifan's activity in both in vitro and in vivo models of SARS-CoV-2 infection.
Main Methods:
- In vitro assays using human lung adenocarcinoma (Calu3) and primary human small airway epithelial cells (HSAEC).
- In vivo studies utilizing a golden Syrian hamster model of SARS-CoV-2 infection.
- Quantification of viral RNA copy numbers and infectious virus titers.
- Histopathological examination of lung tissues.
Main Results:
- Larifan significantly reduced SARS-CoV-2 replication in Calu3 and HSAEC cells (p < 0.05).
- Intranasal administration of Larifan markedly decreased viral load and infectious virus titers in hamster lungs (p < 0.01).
- Treatment with Larifan improved lung histopathology in infected hamsters.
Conclusions:
- Larifan demonstrates significant in vitro and in vivo antiviral activity against SARS-CoV-2.
- The drug effectively reduces viral load and mitigates lung pathology in a hamster model.
- Larifan shows potential as a therapeutic agent for controlling COVID-19 in humans.
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