Antiviral Efficacy of Verdinexor In Vivo in Two Animal Models of Influenza A Virus Infection.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 27893810.
- Also identified by DOI 10.1371/journal.pone.0167221 and PMC identifier 5125695.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Influenza A virus (IAV) causes seasonal epidemics of respiratory illness that can cause mild to severe illness and potentially death. Antiviral drugs are an important countermeasure against IAV; however, drug resistance has developed, thus new therapeutic approaches are being sought. Previously, we demonstrated the antiviral activity of a novel nuclear export inhibitor drug, verdinexor, to reduce influenza replication in vitro and pulmonary virus burden in mice. In this study, in vivo efficacy of verdinexor was further evaluated in two animal models or influenza virus infection, mice and ferrets. In mice, verdinexor was efficacious to limit virus shedding, reduce pulmonary pro-inflammatory cytokine expression, and moderate leukocyte infiltration into the bronchoalveolar space. Similarly, verdinexor-treated ferrets had reduced lung pathology, virus burden, and inflammatory cytokine expression in the nasal wash exudate. These findings support the anti-viral efficacy of verdinexor, and warrant its development as a novel antiviral therapeutic for influenza infection.
Medical subject headings
- Acrylamides
- Active Transport, Cell Nucleus
- Antiviral Agents
- Disease Models, Animal
- Hydrazines
- Influenza A virus
- Orthomyxoviridae Infections