Inhibition of Phosphatidylinositol 3-Kinase by Pictilisib Blocks Influenza Virus Propagation in Cells and in Lungs of Infected Mice.
Stefanie Deinhardt-EmmerLaura JäckelClio HäringSarah BöttcherJanine J WildenBrigitte GlückRegine HellerMichaela SchmidtkeMirijam KochBettina LöfflerStephan LudwigChristina EhrhardtPublished in: Biomolecules (2021)
Influenza virus (IV) infections are considered to cause severe diseases of the respiratory tract. Beyond mild symptoms, the infection can lead to respiratory distress syndrome and multiple organ failure. Occurrence of resistant seasonal and pandemic strains against the currently licensed antiviral medications points to the urgent need for new and amply available anti-influenza drugs. Interestingly, the virus-supportive function of the cellular phosphatidylinositol 3-kinase (PI3K) suggests that this signaling module may be a potential target for antiviral intervention. In the sense of repurposing existing drugs for new indications, we used Pictilisib, a known PI3K inhibitor to investigate its effect on IV infection, in mono-cell-culture studies as well as in a human chip model. Our results indicate that Pictilisib is a potent inhibitor of IV propagation already at early stages of infection. In a murine model of IV pneumonia, the in vitro key findings were verified, showing reduced viral titers as well as inflammatory response in the lung after delivery of Pictilisib. Our data identified Pictilisib as a promising drug candidate for anti-IV therapies that warrant further studying. These results further led to the conclusion that the repurposing of previously approved substances represents a cost-effective and efficient way for development of novel antiviral strategies.
Keyphrases
- respiratory tract
- inflammatory response
- protein kinase
- sars cov
- endothelial cells
- randomized controlled trial
- induced apoptosis
- drug induced
- escherichia coli
- high throughput
- risk assessment
- coronavirus disease
- metabolic syndrome
- case report
- big data
- high fat diet induced
- anti inflammatory
- oxidative stress
- artificial intelligence
- signaling pathway
- adverse drug
- depressive symptoms