Asthma is an inflammatory disease of the airways. After allergen exposure, IgE bearing cells, such as mast cells and basophils, are first activated. Later, T lymphocytes enter the airways, are activated by allergen and play a key role in regulating this inflammatory response through the elaboration of cytokines such as IL-4, IL-5 and IFN-gamma. This project seeks to examine the cytokine and mediator profiles of mast cell, basophil and T cell subpopulations that may be involved in the generation of inflammation in asthmatic airways. We have developed sensitive intracellular cytokine assays to measure allergen specific T cell cytokine responses almost directly ex vivo. Using these methods, we have shown that allergen specific T cells are predominantly of the classic Th2 phenotype and that on the single cell level IL-4, IL-5 and IL-13 are highly co-expressed. Interestingly, IL-2, which is often considered a Th1 cytokine was also highly coexpressed. Allergen specific T cell expressed high levels of the CCR4 and CRTH2 chemoattractant receptors. These results provide a detailed view of the T cell response to allergens with a fidelity heretofore not possible.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000709-11
Application #
6986006
Study Section
(LAD)
Project Start
Project End
Budget Start
Budget End
Support Year
11
Fiscal Year
2004
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code
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