1 immunized with ovalbumin and challenged with aerosolized antigen.

2 umin and challenged through the airways with aerosolized antigen, are severely impaired in their abil

3 s, or induction of airway hyperreactivity to aerosolized antigen, beta 2m-deficient mice developed fu

4  up-regulated in the lungs of mice following aerosolized antigen challenge of sensitized mice, and du

5 f nodose neurons isolated 24 h after in vivo aerosolized antigen challenge of the airway were depolar

6 onsiveness to methacholine in the absence of aerosolized antigen challenge.

7 e level of intraepithelial MC in the lung of aerosolized, antigen-challenged mice.

8 4 microM), was efficacious in the guinea pig aerosolized antigen induced airway obstruction assay (ED

9 ompound 18 was efficacious in the guinea pig aerosolized antigen induced airway obstruction assay (ED

10 0L interactions at the time of inhalation of aerosolized antigen suppressed memory effector accumulat

11 nduced by repeated exposure to a low dose of aerosolized antigen, we show an important contribution b