Institute of Medical Microbiology, Jena University Hospital, Am Klinikum 1, D-07747 Jena, Germany.
Section of Experimental Virology, Institute of Medical Microbiology, Center for Molecular Biomedicine (CMB), Jena University Hospital, Hans-Knoell-Str. 2, D-07745 Jena, Germany.
Biomolecules. 2021 May 29;11(6):808. doi: 10.3390/biom11060808.
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.
流感病毒(IV)感染被认为会导致严重的呼吸道疾病。除了轻度症状外,感染还可能导致呼吸窘迫综合征和多器官衰竭。目前已获许可的抗病毒药物对季节性和大流行株的耐药性表明,迫切需要新的、大量可用的抗流感药物。有趣的是,细胞磷脂酰肌醇 3-激酶(PI3K)的病毒支持功能表明,该信号模块可能是抗病毒干预的潜在靶点。为了将现有药物重新用于新的适应症,我们使用了 Pictilisib,一种已知的 PI3K 抑制剂,在单核细胞培养研究以及人类芯片模型中研究其对 IV 感染的影响。我们的结果表明,Pictilisib 是一种有效的 IV 复制抑制剂,在感染的早期阶段就已经有效。在 IV 肺炎的小鼠模型中,体外的关键发现得到了验证,在给予 Pictilisib 后,肺部的病毒滴度和炎症反应均降低。我们的数据将 Pictilisib 确定为抗 IV 治疗的有前途的候选药物,值得进一步研究。这些结果进一步得出结论,即重新利用先前批准的物质代表了开发新型抗病毒策略的一种具有成本效益和高效的方法。