Author: Scagnolari, Carolina; Vicenzi, Elisa; Bellomi, Francesca; Stillitano, Maria Giuseppina; Pinna, Debora; Poli, Guido; Clementi, Massimo; Dianzani, Ferdinando; Antonelli, Guido
                    Title: Increased sensitivity of SARS-coronavirus to a combination of human type I and type II interferons.  Cord-id: wxp7rls0  Document date: 2004_1_1
                    ID: wxp7rls0
                    
                    Snippet: There is currently an urgent need to identify effective antiviral agents that will prevent and treat severe acute respiratory syndrome coronavirus (SARS-CoV) infection. In this study, we have investigated and compared the antiviral effect of different interferons (IFNs) on SARS-CoV replication in the epithelial kidney monkey Vero cell line. The results showed that SARS-CoV grown in Vero cells is moderately sensitive to IFN-beta and only weakly sensitive to IFN-alpha and IFN-gamma, in comparison 
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: There is currently an urgent need to identify effective antiviral agents that will prevent and treat severe acute respiratory syndrome coronavirus (SARS-CoV) infection. In this study, we have investigated and compared the antiviral effect of different interferons (IFNs) on SARS-CoV replication in the epithelial kidney monkey Vero cell line. The results showed that SARS-CoV grown in Vero cells is moderately sensitive to IFN-beta and only weakly sensitive to IFN-alpha and IFN-gamma, in comparison to other IFN-sensitive viruses, such as those for encephalomyocarditis, vesicular stomatitis and Newcastle disease. Simultaneous incubation of Vero cells with IFN-beta and IFN-gamma indicated that they may act synergistically against SARS-CoV replication. The IFN-induced MxA protein was detected in the IFN-treated Vero cells. The data, however, suggest that the antiviral activity of IFN against SARS-CoV virus is independent of MxA expression.
 
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