Identifying enhancers of innate immune signaling as broad-spectrum antivirals active against emerging viruses
- Cell Chem Biol. 2022 Jul 21;29(7):1113-1125.e6. doi: 10.1016/j.chembiol.2022.05.009.
- 1. Viral Trafficking, Restriction and Innate Signaling, Institut de Recherche en Infectiologie de Montpellier (IRIM), Université de Montpellier, CNRS, 34090 Montpellier, France.
- 2. Department of Microbiology and Molecular Medicine, University of Geneva School of Medicine, CMU, 1211 Geneva 4, Switzerland.
- 3. Membrane Dynamics & Viruses, Institut de Recherche en Infectiologie de Montpellier (IRIM), Université de Montpellier, CNRS, 34090 Montpellier, France.
- 4. Viral Trafficking, Restriction and Innate Signaling, Institut de Recherche en Infectiologie de Montpellier (IRIM), Université de Montpellier, CNRS, 34090 Montpellier, France. Electronic address: [email protected].
- 5. Viral Trafficking, Restriction and Innate Signaling, Institut de Recherche en Infectiologie de Montpellier (IRIM), Université de Montpellier, CNRS, 34090 Montpellier, France. Electronic address: [email protected].
The increasingly frequent outbreaks of pathogenic viruses have underlined the urgent need to improve our arsenal of antivirals that can be deployed for future pandemics. Innate immunity is a powerful first line of defense against pathogens, and compounds that boost the innate response have high potential to act as broad-spectrum antivirals. Here, we harnessed localization-dependent protein-complementation assays (called Alpha Centauri) to measure the nuclear translocation of interferon regulatory factors (IRFs), thus providing a readout of innate immune activation following viral Infection that is applicable to high-throughput screening of immunomodulatory molecules. As proof of concept, we screened a library of kinase inhibitors on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Infection and identified Gilteritinib as a powerful enhancer of innate responses to viral Infection. This immunostimulatory activity of Gilteritinib was found to be dependent on the AXL-IRF7 axis and results in a broad and potent Antiviral activity against unrelated RNA viruses.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: mTOR; FKBP; Molecular Glues; Fungal; Autophagy; Endogenous Metabolite; Antibiotic; Bacterial
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Research Areas: Cancer
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Research Areas: Cancer
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Research Areas: Infection
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Research Areas: Cancer
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Research Areas: Infection
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target: IKKResearch Areas: Metabolic Disease
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target: c-Fms
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Research Areas: Cancer
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Research Areas: Infection
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