mortality/aging
• in mice infected with West Nile Virus
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immune system
• of CD8+ T cells in mice infected with West Nile Virus 10 days post-infection
• of CD8+ T cells in mice infected with lymphocytic choriomeningitis virus
• regulation of cell survival is cell-intrinsic
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• macrophages and dendritic cells infected with West Nile Virus exhibit reduced IFN-beta production compared with wild-type cells
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• in re-stimulated splenocytes and CD8+ T cells from mice infected with West Nile Virus
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• in re-stimulated splenocytes and CD8+ T cells from mice infected with West Nile Virus
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• macrophages and dendritic cells infected with West Nile Virus exhibit reduced IFN-beta production and increased virus replication (24 hr post-infection) compared with wild-type cells
• mice infected with West Nile Virus exhibit extensive neuron damage, increased viral load and reduced CD8+ T cells numbers in the brain and spleen increased apoptosis (10 days post-infection) compared with wild-type mice
• mice infected with lymphocytic choriomeningitis virus exhibit increased CD8+ T cell apoptosis compared with wild-type mice
• however, mice infected with West Nile Virus exhibit normal innate immune response and viral replication in neurons
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• in mice infected with West Nile Virus
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cellular
• of CD8+ T cells in mice infected with West Nile Virus 10 days post-infection
• of CD8+ T cells in mice infected with lymphocytic choriomeningitis virus
• regulation of cell survival is cell-intrinsic
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hematopoietic system
• of CD8+ T cells in mice infected with West Nile Virus 10 days post-infection
• of CD8+ T cells in mice infected with lymphocytic choriomeningitis virus
• regulation of cell survival is cell-intrinsic
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