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The relationship between late asthmatic responses and antigen-specific immunoglobulin
S Waserman1, R Olivenstein, P Renzi
1Meakins-Christie Laboratories, McGill University, Montreal, Quebec, Canada.
The Journal of Allergy and Clinical Immunology
|October 1, 1992
Summary
Allergen-induced airway responses in rats were studied alongside immune markers. Specific IgG levels inversely correlated with early airway responses, but not late responses, suggesting different underlying mechanisms.
Area of Science:
- Immunology
- Respiratory Medicine
- Allergy Research
Background:
- Allergen exposure can trigger immediate (early) and delayed (late) airway responses.
- The relationship between specific antibodies (IgE, IgG), lymphocyte subsets, and these airway responses requires further elucidation.
Purpose of the Study:
- To investigate the correlation between allergen-induced early and late airway responses.
- To examine the association of antigen-specific IgE, IgG, and lymphocyte subsets with these airway responses in blood and bronchoalveolar lavage (BAL).
Main Methods:
- Brown Norway rats were sensitized with ovalbumin and Bordetella pertussis.
- Animals were challenged with ovalbumin aerosol, and lung resistance was measured over 8 hours.
- Ovalbumin-specific IgE and IgG levels were quantified using ELISA; lymphocyte subsets were analyzed.
Main Results:
- Ovalbumin-specific IgE and IgG levels increased after sensitization, peaking at 3 weeks.
- IgE levels did not correlate with early or late airway responses.
- A significant inverse correlation was found between specific IgG and the early response, but not the late response. Lymphocyte subset ratios showed no correlation with airway responses.
Conclusions:
- Early and late airway responses appear to be driven by distinct mechanisms, despite a correlation between their magnitudes.
- Specific IgG levels are inversely associated with the early phase of allergen-induced airway hyperresponsiveness.
- Neither IgE nor lymphocyte subsets correlated with the magnitude of early or late airway responses in this model.
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