Seldeslachts Laura, Jacobs Cato, Tielemans Birger, Vanhoffelen Eliane, Van der Sloten Lauren, Humblet-Baron Stephanie, Naesens Lieve, Lagrou Katrien, Verbeken Erik, Wauters Joost, Vande Velde Greetje
Biomedical MRI Unit/MoSAIC, Department of Imaging and Pathology, KU Leuven, 3000 Leuven, Belgium.
Laboratory for Clinical Infectious and Inflammatory Disorders, Department of Microbiology, Immunology and Transplantation, KU Leuven, 3000 Leuven, Belgium.
J Fungi (Basel). 2021 Dec 21;8(1):1. doi: 10.3390/jof8010001.
Influenza-associated pulmonary aspergillosis (IAPA) is a global recognized superinfection in critically ill influenza patients. Baloxavir marboxil, a cap-dependent endonuclease inhibitor, is a newly approved anti-influenza therapeutic. Although the benefits as a treatment for influenza are clear, its efficacy against an influenza- co-infection has yet to be determined. We investigated the therapeutic effect of baloxavir marboxil in a murine model for IAPA. Immunocompetent mice received intranasal instillation of influenza A followed by orotracheal inoculation with 4 days later. Administration of baloxavir marboxil or sham was started at day 0, day 2 or day 4. Mice were monitored daily for overall health status, lung pathology with micro-computed tomography (µCT) and fungal burden with bioluminescence imaging (BLI). In vivo imaging was supplemented with virological, mycological and biochemical endpoint investigations. We observed an improved body weight, survival and viral clearance in baloxavir marboxil treated mice. µCT showed less pulmonary lesions and bronchial dilation after influenza and after co-infection in a treatment-dependent pattern. Furthermore, baloxavir marboxil was associated with effective inhibition of fungal invasion. Hence, our results provide evidence that baloxavir marboxil mitigates severe influenza thereby decreasing the susceptibility to a lethal invasive superinfection.
流感相关肺曲霉病(IAPA)是一种在重症流感患者中全球公认的二重感染。巴洛沙韦酯是一种帽依赖性内切核酸酶抑制剂,是一种新批准的抗流感治疗药物。虽然其作为流感治疗药物的益处是明确的,但其对流感合并感染的疗效尚未确定。我们在IAPA小鼠模型中研究了巴洛沙韦酯的治疗效果。免疫功能正常的小鼠经鼻内滴注甲型流感病毒,4天后经口气管接种。在第0天、第2天或第4天开始给予巴洛沙韦酯或假处理。每天监测小鼠的整体健康状况、用微型计算机断层扫描(µCT)观察肺部病理情况以及用生物发光成像(BLI)观察真菌负荷。体内成像辅以病毒学、真菌学和生化终点研究。我们观察到巴洛沙韦酯治疗的小鼠体重增加、存活率提高且病毒清除。µCT显示在流感及合并感染后,肺部病变和支气管扩张减少,且呈治疗依赖性模式。此外,巴洛沙韦酯与有效抑制真菌侵袭有关。因此,我们的结果提供了证据,证明巴洛沙韦酯可减轻重症流感,从而降低致死性侵袭性二重感染的易感性。