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Epithelial damage and angiogenesis in the airways of children with asthma
Angelo Barbato1, Graziella Turato, Simonetta Baraldo
1Divisione di Pneumologia, Dipartimento di Scienze Cardiologiche, Toraciche e Vascolari Università degli Studi di Padova, via Giustiniani 3, Padova, Italy.
Insights
Childhood asthma shows airway remodeling, including epithelial damage and thickened basement membranes, similar to adults. These changes, along with eosinophilia, appear early in the disease and may also indicate atopy without asthma symptoms.
Area of Science:
- Pediatric Pulmonology
- Respiratory Medicine
- Immunology
Background:
- Airway remodeling and inflammation are hallmarks of adult asthma.
- These pathological features are under-investigated in pediatric asthma cases.
Purpose of the Study:
- To investigate epithelial and vascular changes in pediatric asthma.
- To assess the inflammatory response within the airways of children with asthma.
Main Methods:
- Analysis of bronchial biopsies from 44 children (17 mild/moderate asthma, 12 atopy without asthma, 15 controls).
- Histochemistry and immunohistochemistry used to quantify epithelial loss, basement membrane thickness, vascularity, and inflammatory cells.
- Stratified analysis by age was performed.
Main Results:
- Children with asthma exhibited increased epithelial loss and basement membrane thickness compared to controls and atopic children.
- Increased vascularity and eosinophils were observed in both asthmatic and atopic children without asthma, compared to controls.
- Younger children (<6 years) with asthma showed significantly increased epithelial loss, basement membrane thickening, and eosinophilia.
Conclusions:
- Pathological airway changes, characteristic of adult asthma, are present even in childhood asthma.
- Airway eosinophilia and increased vascularity (angiogenesis) were also noted in atopic children without asthma.
- These findings suggest that airway lesions develop early in asthma's natural history and may be indicative of atopy, even before asthma symptoms manifest.
Rationale:
Airway remodeling and inflammation are characteristic features of adult asthma that are still poorly investigated in childhood asthma.
Objectives:
To examine epithelial and vascular changes as well as the inflammatory response in airways of children with asthma.
Methods:
We analyzed bronchial biopsies obtained from 44 children undergoing bronchoscopy for appropriate clinical indications other than asthma: 17 with mild/moderate asthma (aged 2-15 yr), 12 with atopy without asthma (1-11 yr), and 15 control children without atopy or asthma (1-14 yr). By histochemistry and immunohistochemistry, we quantified epithelial loss, basement membrane thickness, number of vessels, and inflammatory cells in subepithelium.
Results:
Epithelial loss and basement membrane thickness were increased in children with asthma compared with control subjects (p = 0.005 and p = 0.0002, respectively) and atopic children (p = 0.002 and p = 0.005, respectively). The number of vessels and eosinophils was increased not only in asthmatic children (p = 0.03 and p = 0.0002, respectively) but also in atopic children without asthma (p = 0.03 and p = 0.008, respectively) compared with control subjects. When we stratified the analysis according to age, we observed that children with asthma younger than 6 yr had increased epithelial loss, basement membrane thickening, and eosinophilia compared with control subjects of the same age.
Conclusions:
Epithelial damage and basement membrane thickening, which are pathologic features characteristic of adult asthma, are present even in childhood asthma. Other changes, such as airway eosinophilia and angiogenesis, were also observed in atopic children without asthma. These observations suggest that pathologic changes occur early in the natural history of asthma and emphasize the concept that some of these lesions may characterize atopy even in the absence of asthmatic symptoms.
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