NHC Key Laboratory of Biosafety, NHC Key Laboratory of Medical Virology and Viral Diseases, Chinese National Influenza Center, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China; National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
NHC Key Laboratory of Biosafety, NHC Key Laboratory of Medical Virology and Viral Diseases, Chinese National Influenza Center, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China.
Clin Immunol. 2024 May;262:110178. doi: 10.1016/j.clim.2024.110178. Epub 2024 Mar 8.
Controlling the excessive inflammatory response is one of the key ways to reduce the severity and mortality of severe influenza virus infections. RAGE is involved in inflammatory responses and acute lung injuries. Here, we investigated the role of RAGE and its potential application as a target for severe influenza treatment through serological correlation analysis for influenza patients, and treatment with the RAGE inhibitor FPS-ZM1 on A549 cells or mice with influenza A (H1N1) infection. The results showed high levels of RAGE were correlated with immunopathological injury and severity of influenza, and FPS-ZM1 treatment increased the viability of A549 cells with influenza A infection and decreased morbidity and mortality of influenza A virus infection in mice. The RAGE/NF-κb inflammatory signaling pathway is a major targeting pathway for FPS-ZM1 treatment in severe influenza. These findings provide further insights into the immune injury of severe influenza and a potential targeting candidate for the disease treatment.
控制过度的炎症反应是减轻严重流感病毒感染严重程度和死亡率的关键方法之一。RAGE 参与炎症反应和急性肺损伤。在这里,我们通过对流感患者的血清学相关性分析,以及用 RAGE 抑制剂 FPS-ZM1 处理感染甲型流感(H1N1)的 A549 细胞或小鼠,研究了 RAGE 的作用及其作为严重流感治疗靶点的潜力。结果表明,高水平的 RAGE 与流感的免疫病理损伤和严重程度相关,FPS-ZM1 处理可提高感染甲型流感的 A549 细胞的活力,并降低小鼠感染甲型流感病毒的发病率和死亡率。RAGE/NF-κb 炎症信号通路是 FPS-ZM1 治疗严重流感的主要作用靶点。这些发现为严重流感的免疫损伤提供了进一步的认识,并为该疾病的治疗提供了一个潜在的靶点候选物。