Cho Junhyung, Yi Hwajung, Jang Eun Young, Lee Mi-Seon, Lee Joo-Yeon, Kang Chun, Lee Chan Hee, Kim Kisoon
Division of Viral Disease Research, Center for Infectious Diseases Research, Korea National Institute of Health, Cheongju, Republic of Korea; Department of Microbiology, Chungbuk National University, Cheongju, Republic of Korea.
Division of Viral Disease Research, Center for Infectious Diseases Research, Korea National Institute of Health, Cheongju, Republic of Korea.
Biochem Biophys Res Commun. 2017 Dec 9;494(1-2):298-304. doi: 10.1016/j.bbrc.2017.10.037. Epub 2017 Oct 7.
Infection with the highly pathogenic avian influenza H5N1 virus results in a high incidence of mortality in humans. Severe complications from infection are often associated with hypercytokinemia. However, current neuraminidase inhibitors (NAIs) have several limitations including the appearance of oseltamivir-resistant H5N1 virus and the inability to completely ameliorate hyper-immune responses. To overcome these limitations, we evaluated the anti-viral activity of mycophenolic mofetil (MMF) against A/Vietnam/1194/2004 (H5N1) virus infection using MDCK cells and mice. The IC of MMF (0.94 μM) was comparable to that of zanamivir (0.87 μM) in H5N1 virus-infected MDCK cells based on ELISA. Time-course assays demonstrated that MMF completely inhibited H5N1 viral mRNA replication and protein expression for approximately 8 h after the initiation of treatment. In addition, MMF treatment protected 100% of mice, and lung viral titers were substantially reduced. The anti-viral mechanism of MMF against H5N1 virus infection was further confirmed to depend on the inhibition of cellular inosine monophosphate dehydrogenase (IMPDH) by exogenous guanosine, which inhibits viral mRNA and protein expression. Moreover, IL-1β, IFN-β, IL-6, and IP-10 mRNA expression levels were significantly downregulated in MDCK cells with MMF treatment. These results indicated that MMF could represent a novel inhibitor of viral replication and a potent immunomodulator for the treatment of H5N1 virus infection.
感染高致病性禽流感H5N1病毒会导致人类高死亡率。感染引发的严重并发症通常与高细胞因子血症有关。然而,目前的神经氨酸酶抑制剂(NAIs)存在若干局限性,包括出现对奥司他韦耐药的H5N1病毒以及无法完全改善过度免疫反应。为克服这些局限性,我们使用MDCK细胞和小鼠评估了霉酚酸酯(MMF)对A/越南/1194/2004(H5N1)病毒感染的抗病毒活性。基于ELISA,在H5N1病毒感染的MDCK细胞中,MMF的IC(0.94 μM)与扎那米韦的IC(0.87 μM)相当。时间进程分析表明,MMF在开始治疗后约8小时可完全抑制H5N1病毒mRNA复制和蛋白质表达。此外,MMF治疗可保护100%的小鼠,且肺病毒滴度大幅降低。MMF对H5N1病毒感染的抗病毒机制进一步证实依赖于外源性鸟苷对细胞肌苷单磷酸脱氢酶(IMPDH)的抑制,从而抑制病毒mRNA和蛋白质表达。此外,MMF处理的MDCK细胞中IL-1β、IFN-β、IL-6和IP-10 mRNA表达水平显著下调。这些结果表明,MMF可能是一种新型的病毒复制抑制剂和治疗H5N1病毒感染的有效免疫调节剂。