The synergistic interaction of interferon types I and II leads to marked reduction in severe acute respiratory syndrome-associated coronavirus replication and increase in the expression of mRNAs for interferon-induced proteins

被引:14
|
作者
Scagnolari, Carolina
Trombetti, Simona
Alberelli, Alessia
Cicetti, Simona
Bellarosa, Daniela
Longo, Roberta
Spano, Alberto
Riva, Elisabetta
Clementi, Massimo
Antonelli, Guido
机构
[1] Univ Roma La Sapienza, Virol Sect, Dept Expt Med, IT-00185 Rome, Italy
[2] S Pertini Hosp, Rome, Italy
[3] Menarini Ric SpA, Dept Pharmacol, Pomezia, Italy
[4] Ist Sci San Raffaele, Microbiol & Virol Lab, I-20132 Milan, Italy
[5] Univ Vita Salute San Raffaele, Sch Med, Milan, Italy
关键词
interferon; severe acute respiratory syndrome coronavirus; 2 '-5 '-oligoadenylate synthetase; p56;
D O I
10.1159/000098242
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Interferon (IFN)-alpha, -beta and -gamma have been shown to be only marginally effective against severe acute respiratory syndrome coronavirus (SARS-CoV) replication in Vero cell lines. We investigated the combination of type I IFNs (IFN-alpha or -beta) and IFN-gamma for antiviral activity and found that such combinations synergistically inhibited SARS-CoV replication in Vero cells, using yield reduction assay and the isobologram and combination index methods of Chou and Talalay for evaluation. The highly synergistic anti-SARS-CoV action of type I IFNs and IFN-gamma parallels the marked increase in 2'-5'-oligoadenylate synthetase and p56 mRNAs following exposure in Vero cells to either IFN-alpha or -beta and IFN-gamma compared with the transcriptional levels obtained after stimulation with either IFN alone. These results demonstrate that SARS-CoV, although only moderately sensitive to the antiviral action of the individual types of IFN, is highly sensitive to a combination of type I and II IFNs, which suggests that such combinations may have potential in the treatment of SARS-CoV infections. Copyright (c) 2007 S. Karger AG, Basel
引用
收藏
页码:156 / 160
页数:5
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