Zhang Zhaopei, Zhang Shouping, Wang Sanhu
Henan Institute of Science and Technology, Xinxiang 453003, China.
Henan Institute of Science and Technology, Xinxiang 453003, China; Postdoctoral Research Base, Henan Institute of Science and Technology, Xinxiang 453003, China; Post-doctoral Research Station, Henan Agriculture University, Zhengzhou 450002, China.
Microb Pathog. 2017 Feb;103:155-161. doi: 10.1016/j.micpath.2016.12.024. Epub 2016 Dec 27.
The emergence of anti-influenza A virus drugs resistant strain highlights the need for more effective therapy. Our earlier study demonstrated that c-jun, a downstream molecule of JNK, might be important in viral infections and inflammatory responses. In the present study, we explored the function of DNAzymes Dz13 that target c-jun in influenza A virus infected mice. Dz13 displayed non-toxic side effects on A549 cells and BALB/c mice. Moreover, Dz13-treated mice had enhanced survival after influenza compared with untreated mice. Simultaneously, the pulmonary inflammatory responses and viral burden were decreased in Dz13 treated mice. Furthermore, proliferation levels of infection-induced CD4 and CD8 T cells were impaired. These data demonstrated that Dz13 could reduce viral replication and inflammatory response in vivo, suggesting that Dz13 may potentially be used to treat influenza A viral infection.
抗甲型流感病毒耐药株的出现凸显了对更有效治疗方法的需求。我们早期的研究表明,c-jun作为JNK的下游分子,可能在病毒感染和炎症反应中起重要作用。在本研究中,我们探讨了靶向c-jun的脱氧核酶Dz13在甲型流感病毒感染小鼠中的功能。Dz13对A549细胞和BALB/c小鼠无毒性副作用。此外,与未治疗的小鼠相比,经Dz13治疗的小鼠在感染流感后存活率提高。同时,Dz13治疗的小鼠肺部炎症反应和病毒载量降低。此外,感染诱导的CD4和CD8 T细胞的增殖水平受损。这些数据表明,Dz13可以在体内减少病毒复制和炎症反应,提示Dz13可能有潜力用于治疗甲型流感病毒感染。