growth/size/body
• approximately 1/5 of mice runts
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immune system
• production of IFNB, IL6, and IL12b in peritoneal macrophages after infection with Newcastle disease virus (NDV) or vesicular stomatitis virus (VSV) but not after infection with encephalomyocarditis virus is abrogated
• production of IFNB and IL6 is also impaired after NDV or VSV infection in bone marrow derived dendritic cells or MEFs
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• by peritoneal macrophages after infection with Newcastle disease virus (NDV) or vesicular stomatitis virus (VSV) but not after infection with encephalomyocarditis virus
• production of IFNB is also impaired after NDV or VSV infection in bone marrow derived dendritic cells or MEFs
• however, production of IFNB by plasmacytoid dendritic cells after NDV or VSV infection is similar to controls
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• by peritoneal macrophages after infection with Newcastle disease virus (NDV) or vesicular stomatitis virus (VSV) but not after infection with encephalomyocarditis virus
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• by peritoneal macrophages after infection with Newcastle disease virus (NDV) or vesicular stomatitis virus (VSV) but not after infection with encephalomyocarditis virus
• production of IL6 is also impaired after NDV or VSV infection in bone marrow derived dendritic cells or MEFs
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