immune system
• decreased levels of CD80, CD86, and MHC-II in bone marrow derived macrophages in response to H37Rv infection
• however, expression of IL1B, IL6, or TNF-alpha are similar to controls in response to H37Rv infection
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• bone marow derived macrophages show reduced phagocytic activity when challenged with H37Rv labeled with RFP or when incubated with FITC-latex beads
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• isolated bone marrow derived macrophages show reduced IFNalpha and beta secretion after RNA virus infection by vesicular stomatitis virus, encephalomyocarditis virus, or H1N1 influenza A virus but not herpes simplex virus type 1
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• decreased in the peripheral blood and in the lung and spleen at 1 week after M. tuberculosis infection
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• decreased in the peripheral blood and in the lung and spleen at 1 week after M. tuberculosis infection
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• decreased TNF in the peripheral blood and in the lung and spleen at 1 week after M. tuberculosis infection
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• isolated bone marrow derived macrophages show reduced IFNalpha and beta secretion after RNA virus infection by vesicular stomatitis virus, encephalomyocarditis virus, or H1N1 influenza A virus but not herpes simplex virus type 1
• enhanced replication of VSV in the lung and liver and reduced secretion of IFNA and IFNB following infection through the caudal vein
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• isolated bone marrow derived macrophages show reduced IFNalpha and beta secretion after RNA virus infection by vesicular stomatitis virus, encephalomyocarditis virus, or H1N1 influenza A virus but not herpes simplex virus type 1
• enhanced replication of VSV in the lung and liver and reduced secretion of IFNA and IFNB following infection through the caudal vein
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• isolated bone marrow derived macrophages show reduced IFNalpha and beta secretion after RNA virus infection including by vesicular stomatitis virus (VSV), encephalomyocarditis virus (EMCV), or H1N1 influenza A virus but not herpes simplex virus type 1 (HSV1)
• isolated bone marrow derived macrophages show elevated viral mRNA levels after RNA virus infection including by VSV, EMCV, or H1N1 but not HSV1
• isolated MEFs show reduced IFN-beta secretion after RNA virus infection including by vesicular stomatitis virus or encephalomyocarditis virus
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• elevated bacterial loads following M. tuberculosis infection, marked tissue damage in the lungs, and inflammatory infiltration in both the lungs and spleen
• suppressed production of bactericidal NO following M. tuberculosis infection
• intracellular multiplication of M. tuberculosis in bone marrow derived macrophages is enhanced
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• one day after VSV infection 80% of mice display conjunctivitis
• enhanced replication of VSV in the lung and liver and reduced secretion of IFNA and IFNB following infection through the caudal vein
• increased infiltration of inflammatory cells into the lungs following VSV infection and decreased resistance in overall survival assays
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homeostasis/metabolism
• markedly repressed in bone marrow derived macrophages
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• decreased in the peripheral blood and in the lung and spleen at 1 week after M. tuberculosis infection
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• decreased in the peripheral blood and in the lung and spleen at 1 week after M. tuberculosis infection
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• decreased TNF in the peripheral blood and in the lung and spleen at 1 week after M. tuberculosis infection
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cellular
• markedly repressed in bone marrow derived macrophages
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• bone marow derived macrophages show reduced phagocytic activity when challenged with H37Rv labeled with RFP or when incubated with FITC-latex beads
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hematopoietic system
• decreased levels of CD80, CD86, and MHC-II in bone marrow derived macrophages in response to H37Rv infection
• however, expression of IL1B, IL6, or TNF-alpha are similar to controls in response to H37Rv infection
|
• bone marow derived macrophages show reduced phagocytic activity when challenged with H37Rv labeled with RFP or when incubated with FITC-latex beads
|
• isolated bone marrow derived macrophages show reduced IFNalpha and beta secretion after RNA virus infection by vesicular stomatitis virus, encephalomyocarditis virus, or H1N1 influenza A virus but not herpes simplex virus type 1
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