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• W1566175273 endingPage "4940" @default.
• W1566175273 startingPage "4933" @default.
• W1566175273 abstract "Human asthma is characterized by increased airway hyperreactivity to a variety of bronchoconstricting agents. Aberrant type 2 immune responses in the lung have been associated with airway hyperreactivity in both human asthma and in murine models of allergic airways disease. Despite their intrinsically elevated basal airway reactivity to smooth muscle constricting agents, A/J mice demonstrated no inherent inflammatory cell infiltration nor elevation of type 2 cytokines in the lung. Crossed bone marrow reconstitution experiments between A/J and MHC congenic B10.A mice revealed enhanced airway reactivity only in A/J recipients, irrespective of whether they had been reconstituted with A/J or B10. A hemopoietic cells. Further, A/J-derived bone marrow cells did not affect the reactivity of B10.A recipients. Although mice on RAG-deficient and IL-4-deficient backgrounds demonstrate substantial abrogation of allergen-induced airway hyperreactivity, these gene deletions had no impact on the elevated baseline reactivity when backcrossed onto A/J mice. Thus, in these mice, basal airway hyperreactivity is maintained independently of type 2 immunity induced by allergens." @default.
• W1566175273 created "2016-06-24" @default.
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• W1566175273 date "2000-05-01" @default.
• W1566175273 modified "2023-10-08" @default.
• W1566175273 title "Baseline Airway Hyperreactivity in A/J Mice Is not Mediated by Cells of the Adaptive Immune System" @default.
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• W1566175273 doi "https://doi.org/10.4049/jimmunol.164.9.4933" @default.
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