State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
University of Chinese Academy of Sciences, Beijing, China.
Front Immunol. 2019 Jun 21;10:1393. doi: 10.3389/fimmu.2019.01393. eCollection 2019.
Excessive inflammation associated with the uncontrolled release of pro-inflammatory cytokines is the main cause of death from influenza virus infection. Previous studies have indicated that inhibition of interferon gamma-induced protein 10 (IP-10), interleukin-8 (IL-8), monocyte chemoattractant protein 1 (MCP-1), or their cognate receptors has beneficial effects. Here, by using monocytic U937 cells that capable of secreting the three important cytokines during influenza A virus infection, we measured the inhibitory activities on the production of three cytokines of six anti-inflammatory compounds reported in other models of inflammation. We found that ponatinib had a highly inhibitory effect on the production of all three cytokines. We tested ponatinib in a mouse influenza model to assess its therapeutic effects with different doses and administration times and found that the delayed administration of ponatinib was protective against lethal influenza A virus infection without reducing virus titers. Therefore, we suggest that ponatinib may serve as a new immunomodulator in the treatment of influenza.
与失控的促炎细胞因子释放相关的过度炎症是流感病毒感染导致死亡的主要原因。先前的研究表明,抑制干扰素 γ 诱导蛋白 10(IP-10)、白细胞介素-8(IL-8)、单核细胞趋化蛋白 1(MCP-1)或其同源受体具有有益作用。在这里,我们使用能够在甲型流感病毒感染期间分泌三种重要细胞因子的单核细胞 U937 细胞,测量了六种抗炎化合物在其他炎症模型中对三种细胞因子产生的抑制活性。我们发现 ponatinib 对三种细胞因子的产生均具有高度抑制作用。我们在小鼠流感模型中测试了 ponatinib,以评估不同剂量和给药时间的治疗效果,发现 ponatinib 的延迟给药可预防致死性甲型流感病毒感染,而不会降低病毒滴度。因此,我们认为 ponatinib 可能是治疗流感的一种新型免疫调节剂。