Mycophenolic mofetil, an alternative antiviral and immunomodulator for the highly pathogenic avian influenza H5N1 virus infection

被引:17
|
作者
Cho, Junhyung [1 ,4 ]
Yi, Hwajung [1 ]
Jang, Eun Young [1 ]
Lee, Mi-Seon [1 ,5 ]
Lee, Joo-Yeon [2 ]
Kang, Chun [3 ]
Lee, Chan Hee [4 ]
Kim, Kisoon [1 ]
机构
[1] Korea Natl Inst Hlth, Div Viral Dis Res, Ctr Infect Dis Res, Cheongju, South Korea
[2] Korea Natl Inst Hlth, Div Emerging Infect Dis Vector Res, Ctr Infect Dis Res, Cheongju, South Korea
[3] Korea Ctr Dis Control & Prevent, Div Viral Dis, Ctr Lab Control Infect Dis, Cheongju, South Korea
[4] Chungbuk Natl Univ, Dept Microbiol, Cheongju, South Korea
[5] Pai Chai Univ, Dept Life Sci & Technol, Daejeon, South Korea
关键词
Highly pathogenic avian influenza; H5N1 influenza virus; Mycophenolic mofetil; Immunomodulator; Anti-influenza treatment; LUNG INFLAMMATION; HUMAN-DISEASE; INDUCTION; REPLICATION; ANTIBODIES; IL-1-BETA; CYTOKINES; HUMANS; CELLS; ACID;
D O I
10.1016/j.bbrc.2017.10.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 IC50 of MMF (0.94 mu M) was comparable to that of zanamivir (0.87 mu M) 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 mono phosphate dehydrogenase (IMPDH) by exogenous guanosine, which inhibits viral mRNA and protein expression. Moreover, IL-1 beta, IFN-beta, IL-6, and IP-10 mRNA expression levels were significantly down regulated 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. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:298 / 304
页数:7
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