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The Bovine Lung in Biomedical Research: Visually Guided Bronchoscopy, Intrabronchial Inoculation and In Vivo Sampling Techniques
Published on: July 3, 2014
Bronchoalveolar lavage, histological and immunohistochemical features in cryptogenic organizing pneumonia
V Poletti1, G Castrilli, M Romagna
1Dept of Pulmonary Medicine, Ospedale Maggiore, Bologna, Italy.
Insights
Bronchoalveolar lavage and histology confirm cryptogenic organizing pneumonia (COP). Increased T-lymphocytes and granulocyte/macrophage colony-stimulating factor (GM-CSF) suggest its role in COP pathogenesis.
Area of Science:
- Pulmonary Medicine
- Immunology
- Pathology
Background:
- Cryptogenic organizing pneumonia (COP) is an idiopathic interstitial pneumonia.
- Accurate diagnosis of COP relies on integrating clinical, radiological, and pathological findings.
Purpose of the Study:
- To characterize the bronchoalveolar lavage (BAL) and histological features in patients with COP.
- To investigate the role of specific immune cells and cytokines, such as granulocyte/macrophage colony-stimulating factor (GM-CSF), in COP pathogenesis.
Main Methods:
- Analysis of BAL fluid cell counts and differentials.
- Histopathological examination of lung biopsies (transbronchial and open lung).
- Immunohistochemical staining for cell surface markers (HLA-DR, CD3, CD8, CD45R0) and GM-CSF.
Main Results:
- BAL fluid showed increased lymphocytes, with a decreased CD4/CD8 ratio, and elevated HLA-DR expressing T-lymphocytes.
- Lung specimens revealed Masson bodies, with epithelial cells expressing GM-CSF.
- Immunohistochemistry confirmed a predominance of CD8+ T-lymphocytes and alpha-smooth muscle actin in Masson bodies.
Conclusions:
- The combination of BAL findings and histological evidence strongly supports the diagnosis of COP.
- GM-CSF may play a significant role in the pathogenesis of COP, and its expression is downregulated by glucocorticoid treatment.
Abstract:
This study describes bronchoalveolar lavage (BAL), histological and immunohistochemical features in a series of 10 patients with cryptogenic organizing pneumonia (COP). The histological diagnosis was performed by transbronchial biopsy in seven cases and by open lung biopsy in three cases. All patients showed a marked increase in lymphocytes and a mild increase in neutrophils and eosinophils in BAL fluid. The number of T-lymphocytes expressing human leucocyte antigen-DR (HLA-DR) surface antigen was increased (p < 0.002). The majority of lymphocytes expressed the CD8 phenotype, so that the CD4/CD8 ratio was markedly decreased. Masson bodies were present in the lung specimens of all patients. Most of the epithelial cells surrounding the Masson bodies were immunoreactive with an anti-granulocyte/macrophage colony-stimulating factor (GM-CSF) monoclonal antibody. The great majority of mononuclear cells in the lung specimens showed immunoreactivity with anti-CD3, anti-CD8 and anti-CD45R0 monoclonal antibodies. In the Masson bodies, spindle cells were immunoreactive with anti-alpha smooth muscle (alpha-sm) actin monoclonal antibody. Glucocorticoid treatment (the therapy of choice in COP) downregulated GM-CSF messenger ribonucleic acid (mRNA) expression in lung epithelial cell lines. These findings indicate that the combination of bronchoalveolar lavage cell profile with histological evidence is a valuable means of corroborating a clinical diagnosis of cryptogenic organizing pneumonia, and that granulocyte/macrophage colony-stimulating factor may be one of the cytokines involved in the pathogenesis.
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