cellular
• in cultured MEF in vitro, enhanced cytoplasmic poly(I:C)-induced IFN-beta secretion
• in cultur4ed MEF in vitro, vesicular stomatitis virus replication were decreased and more resistant to infection
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mortality/aging
• more resistant in survival assays upon VSV infection
• show enhanced survival ability
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hematopoietic system
• in isolated peritoneal macrophages in vitro, significantly increased secretion of IFN-beta, tumor necrosis factor alpha, and IL-6 after infection by Sendai virus and vesicular stomatitis virus
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immune system
• when challenged with virus, IFN-beta secretion in serum was significantly increased and viral titer and replication in liver and lung were greatly decreased
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• in isolated peritoneal macrophages in vitro, significantly increased secretion of IFN-beta, tumor necrosis factor alpha, and IL-6 after infection by Sendai virus and vesicular stomatitis virus
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• more resistant in survival assays upon VSV infection
• show enhanced survival ability
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