mortality/aging
• mice develop symptoms of an auto-inflammatory disease and do not survive beyond 6 to 8 weeks of age
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immune system
N |
• when bone marrow is used to repopulate irradiated wild-type mice, in vivo TH1 and TH17 responses are normal
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• when bone marrow is used to repopulate irradiated wild-type mice, intranasal ovalbumin challenge induces reduced ovalbumin-IgE serum levels compared with similarly treated wild-type mice
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• when bone marrow is used to repopulate irradiated wild-type mice, intranasal ovalbumin challenge induces reduced TH2 cells (eosinophils, macrophages, and lymphocytes) migration into the bronchoalveolar lavage compared with similarly treated wild-type mice
• however, TH2 cell polarization is normal
|
• when bone marrow is used to repopulate irradiated wild-type mice, intranasal ovalbumin challenge induces reduced TH2 cells (eosinophils, macrophages, and lymphocytes) migration into the bronchoalveolar lavage and reduced ovalbumin-IgE serum levels compared with similarly treated wild-type mice
|
• mice develop symptoms of an auto-inflammatory disease and do not survive beyond 6 to 8 weeks of age
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hematopoietic system
• when bone marrow is used to repopulate irradiated wild-type mice, intranasal ovalbumin challenge induces reduced ovalbumin-IgE serum levels compared with similarly treated wild-type mice
|
• when bone marrow is used to repopulate irradiated wild-type mice, intranasal ovalbumin challenge induces reduced TH2 cells (eosinophils, macrophages, and lymphocytes) migration into the bronchoalveolar lavage compared with similarly treated wild-type mice
• however, TH2 cell polarization is normal
|