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Differences in nasal cellular infiltrates between allergic children and age-matched controls
J G Vinke1, A KleinJan, L W Severijnen
1Dept of Otorhinolaryngology, Erasmus University Medical Centre Rotterdam, The Netherlands.
The European Respiratory Journal
|June 11, 1999
Summary
Nasal allergies in children show distinct cellular changes in the nasal lining, even before specific allergies are detected. Allergic children have more immunoglobulin E (IgE)-positive cells and mast cells in their nasal tissue compared to non-allergic children.
Area of Science:
- Immunology
- Allergy Research
- Pediatric Medicine
Background:
- Cellular infiltrates in pediatric nasal mucosa are not well understood.
- Allergic rhinitis and asthma are common conditions in children.
- Identifying early cellular markers could improve diagnosis and treatment.
Purpose of the Study:
- To compare nasal mucosal cellular infiltrates in allergic children versus non-allergic controls.
- To investigate the presence of specific immune cells and mediators.
- To determine if cellular changes precede the detection of specific immunoglobulin E (IgE).
Main Methods:
- Biopsy specimens of nasal inferior turbinate were collected from 15 allergic and 15 non-allergic children.
- Immunohistochemistry was used to quantify cells positive for CD1a, CD4, CD8, CD19, CD68, chymase, tryptase, IgE, and major basic protein.
- Allergic status was confirmed by symptoms, total serum IgE, family history, and specific IgE testing.
Main Results:
- Allergic children exhibited significantly higher numbers of IgE-positive cells and mast cells in the nasal epithelium.
- The lamina propria of allergic children showed increased IgE-positive cells and eosinophils.
- Langerhans' cells positive for IgE were found in allergic children with specific IgE to aeroallergens.
Conclusions:
- Nasal cellular infiltrates in allergic children differ significantly from those in non-allergic controls.
- Cellular changes in the nasal mucosa can be detected in atopic children prior to specific serum IgE identification.
- These findings highlight potential early biomarkers for pediatric allergic diseases.