Viral Trafficking, Restriction and Innate Signaling, Institut de Recherche en Infectiologie de Montpellier (IRIM), Université de Montpellier, CNRS, 34090 Montpellier, France.
Department of Microbiology and Molecular Medicine, University of Geneva School of Medicine, CMU, 1211 Geneva 4, Switzerland.
Cell Chem Biol. 2022 Jul 21;29(7):1113-1125.e6. doi: 10.1016/j.chembiol.2022.05.009. Epub 2022 Jun 20.
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.
越来越频繁的致病性病毒爆发凸显了改进我们的抗病毒药物储备的紧迫性,这些药物可用于未来的大流行。先天免疫是抵御病原体的强大第一道防线,而增强先天反应的化合物具有作为广谱抗病毒药物的巨大潜力。在这里,我们利用依赖于定位的蛋白互补测定法(称为“半人马座阿尔法”)来测量干扰素调节因子(IRF)的核易位,从而提供了一种针对病毒感染后先天免疫激活的读数,可适用于免疫调节分子的高通量筛选。作为概念验证,我们在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染上筛选了激酶抑制剂文库,并发现吉列替尼是增强病毒感染先天反应的有力增强剂。发现吉列替尼的这种免疫刺激活性依赖于 AXL-IRF7 轴,并导致针对不相关的 RNA 病毒的广泛而强大的抗病毒活性。