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Subcutaneous late phase responses are augmented during local inhalational tolerance in a murine asthma model
Author(s) -
Singh Anurag,
Thrall Roger S,
Guernsey Linda A,
Carson William F,
Secor Eric R,
Cone Robert E,
Rajan Thiruchandurai V,
Schramm Craig M
Publication year - 2008
Publication title -
immunology and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.999
H-Index - 104
eISSN - 1440-1711
pISSN - 0818-9641
DOI - 10.1038/icb.2008.32
Subject(s) - ovalbumin , medicine , immunology , methacholine , eosinophilia , immunoglobulin e , antigen , allergy , asthma , subcutaneous injection , inhalation , lung , respiratory disease , antibody , anesthesia
Acute exposure of sensitized mice to antigen elicits allergic airway disease (AAD) characterized by Th2 cytokine‐dependent pulmonary eosinophilia, methacholine hyperresponsiveness and antigen‐specific IgE elevation. However, chronic exposure induces a local inhalational tolerance (LIT), with resolution of the airway responses but persistent systemic IgE production. To further determine if systemic immunologic responses were maintained during LIT, we assessed subcutaneous late phase responses to ovalbumin in this model. Sensitized and AAD mice developed small subcutaneous responses to ovalbumin, with footpad thickness increasing to 113.7 and 113.6% of baseline, respectively. In comparison, LIT mice developed marked foot swelling (141.6%). Histologic examination confirmed increased inflammation in the chronic animals, with a significant contribution by eosinophils. Thus, the resolution of airway inflammatory responses with chronic antigen inhalation is a localized response, not associated with loss of systemic responses to antigen.