immune system
• LPS-induced Th2 polarization of bone marrow-derived dendritic cells is impaired
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• mice exhibit impaired low dose LPS-induced Th2 sensitization
• however, mice exhibit normal high dose LPS-induced Th1 sensitization
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• mice treated with low dose LPS fail to exhibit airway hyperresponsiveness or increased serum IgE unlike wild-type mice
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• in the bronchoalveolar lavage fluid of mice stimulated with high dose of LPS
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• in the bronchoalveolar lavage fluid of mice stimulated with high dose of LPS
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• mice treated with low dose LPS fail to exhibit airway hyperresponsiveness or increased serum IgE unlike wild-type mice
• however, high dose LPS results in airway inflammation
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• mice treated with a high dose of LPS exhibit a neutrophil-dominant infiltration in the airways compared with an eosinophil-dominant infiltration in wild-type mice
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respiratory system
• mice treated with a high dose of LPS exhibit a neutrophil-dominant infiltration in the airways compared with an eosinophil-dominant infiltration in wild-type mice
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• mice treated with low dose LPS fail to exhibit airway hyperresponsiveness or increased serum IgE unlike wild-type mice
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homeostasis/metabolism
• in the bronchoalveolar lavage fluid of mice stimulated with high dose of LPS
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hematopoietic system
• LPS-induced Th2 polarization of bone marrow-derived dendritic cells is impaired
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• mice treated with low dose LPS fail to exhibit airway hyperresponsiveness or increased serum IgE unlike wild-type mice
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