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Updated: May 3, 2026

Histological Quantification to Determine Lung Fungal Burden in Experimental Aspergillosis
Published on: March 9, 2018
A pathologic study of allergic bronchopulmonary aspergillosis
R G Slavin1, C W Bedrossian, P S Hutcheson
1Department of Internal Medicine, St. Louis University School of Medicine, MO 63104.
This study details allergic bronchopulmonary aspergillosis in a cystic fibrosis patient. Immunohistologic techniques revealed Aspergillus hyphae and eosinophil-derived proteins contributing to lung inflammation.
Area of Science:
- Pulmonary Medicine
- Immunology
- Pathology
Background:
- Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity reaction to Aspergillus fumigatus.
- Cystic fibrosis (CF) patients are at increased risk for developing ABPA.
- Understanding ABPA pathogenesis is crucial for effective treatment strategies.
Observation:
- A lung biopsy from a 10-year-old boy with CF and ABPA showed bronchocentric inflammation with eosinophils, lymphocytes, plasma cells, and monocytes.
- Microscopy revealed intact elastin in blood vessels but disruption in bronchioles.
- Immunofluorescence detected eosinophil major basic protein deposited extracellularly and within macrophages, with some lymphocytes staining positive for IgE.
Findings:
- Immunoperoxidase staining confirmed septate hyphae of Aspergillus in the lung parenchyma.
- Increased interleukin-2 positive T cells were observed, with a helper to suppressor cell ratio of approximately 2:1.
- Extracellular deposition of eosinophil major basic protein suggests a role in tissue damage.
Implications:
- Advanced immunohistologic techniques provide deeper insights into ABPA pathogenesis.
- Findings highlight the complex interplay between fungal elements, eosinophils, and T cells in CF-related ABPA.
- Further research can explore targeted therapies based on these immunopathologic mechanisms.
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