mortality/aging
• in mice treated with oil-in-water emulsion of trehalose-6,60'-dimycolate (TDM)
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immune system
• TDM-treated mice exhibit less of an increase in draining lymph nodes dendritic cells compared with wild-type mice
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• TDM-treated mice immunized with ovalbumin exhibit reduced footpad swelling and anti-ovalbumin IgG compared with wild-type mice
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• in TDM-treated mice immunized with ovalbumin
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• in mice re-challenged with MOG antigen and pertussis toxin 20 days after immunization for EAE
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• bone marrow-derived dendritic cells and macrophages stimulated with platelets coated in trehalose-6,60'-dimycolate (TDM) or zymosan exhibit reduced MIP-2 secretion compared with wild-type cells
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• TDM-treated bone marrow dendritic cells co-cultured with OT-II cells and OVA323-339 or OVA257-264 peptide or ovalbumin protein fail to exhibit an increase in IFN-gamma and IL17 unlike wild-type cells
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• TDM-treated bone marrow dendritic cells co-cultured with OT-II cells and OVA323-339 peptide fail to exhibit an increase in IFN-gamma and IL17 unlike wild-type cells
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• in bone marrow-derived dendritic cells and macrophages stimulated with platelets coated in TDM or zymosan
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• without skin inflammation in TDM-treated mice
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• mice infected with Mycobacterium bovis BCG exhibit reduced IFN-gamma production in response to PPD compared with wild-type mice
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homeostasis/metabolism
• in mice re-challenged with MOG antigen and pertussis toxin 20 days after immunization for EAE
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• in mice treated with oil-in-water emulsion of trehalose-6,60'-dimycolate (TDM)
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• mice treated with TDM exhibit are resistance to lung inflammation, granuloma and lethality unlike wild-type mice
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hematopoietic system
• TDM-treated mice exhibit less of an increase in draining lymph nodes dendritic cells compared with wild-type mice
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• in TDM-treated mice immunized with ovalbumin
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