mortality/aging
• mice infected with Klebsiella pneumonia die before wild-type mice
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immune system
N |
• mice exhibit normal neutrophil infiltration, phagocytosis of opsonized or nonosponized bacteria and activation of neutrophils
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• following receptor crosslinking
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• following receptor crosslinking
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• elevated frequencies of CD19+, CD22+ cells; B220hi, CD19+ cells; IgD SP cells and B220hi,CD24lo cells
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• potential increase in mature recirculating B cells in the bone marrow
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• in the lungs at 3 and 5 days post-infection with Klebsiella pneumonia
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• in the lungs at only 3 days post-infection with Klebsiella pneumonia
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• in the lungs at 3 and 5 days post-infection with Klebsiella pneumonia
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• in the lungs at 3 and 5 days post-infection with Klebsiella pneumonia
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• in the lungs at 3 and 5 days post-infection with Klebsiella pneumonia
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• progressively increasing lung leukocyte infiltration 3 and 5 days post-infection with Klebsiella pneumonia
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• mice infected with Klebsiella pneumonia die before wild-type mice, exhibit increased bacterial load, progressively increasing levels of inflammatory cytokines (TNFalpha, IFNgamma, IL6 and IL17) in the lungs and progressively increasing lung leukocyte infiltration, and fail to recover from low doses unlike wild-type mice
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• mice infected with Klebsiella pneumonia die before wild-type mice
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respiratory system
• progressively increasing lung leukocyte infiltration 3 and 5 days post-infection with Klebsiella pneumonia
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hematopoietic system
• following receptor crosslinking
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• following receptor crosslinking
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• in the spleen
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• elevated frequencies of CD19+, CD22+ cells; B220hi, CD19+ cells; IgD SP cells and B220hi,CD24lo cells
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• potential increase in mature recirculating B cells in the bone marrow
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cellular
• following receptor crosslinking
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• following receptor crosslinking
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