Proliferation of type II pneumocytes and alteration in their apical surface membrane antigenicity in pulmonary sarcoidosis
| Autor: | Keishi Kubo, Takayuki Honda, Morie Sekiguchi, Muneharu Hayasaka |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Pulmonary and Respiratory Medicine
Cytotoxicity Immunologic Systemic disease Pathology medicine.medical_specialty Cell Count Critical Care and Intensive Care Medicine Sarcoidosis Pulmonary Pulmonary fibrosis medicine Humans Pulmonary pathology Lung business.industry Type-II Pneumocytes Respiratory disease medicine.disease Immunohistochemistry Surfactant protein A Pulmonary Alveoli medicine.anatomical_structure Evaluation Studies as Topic Antigens Surface Sarcoidosis Cardiology and Cardiovascular Medicine business Cell Division |
| Zdroj: | Chest. 116(2) |
| ISSN: | 0012-3692 |
| Popis: | Study objective To evaluate both the proliferation of type II pneumocytes in the alveolitis associated with pulmonary sarcoidosis and any alteration in their surface membrane antigenicity. Materials and methods We investigated 20 transbronchial lung biopsy (TBLB) specimens from 20 patients with pulmonary sarcoidosis, 7 TBLB specimens from 7 sarcoidosis patients without pulmonary involvement, and 19 normal lung specimens, using colloidal iron stain and immunostaining with anti-Thomsen-Friedenreich (TF) antigen and anti-surfactant protein-A monoclonal antibodies. Results The density of type II pneumocytes was significantly higher in the pulmonary sarcoidosis specimens ([mean± SD] 11.1 ± 3.7 per 1 mm alveolar septal length) than in the nonpulmonary sarcoidosis (7.8 ± 1.3) or normal lung specimens (7.2 ± 0.8). TF antigen was directly expressed on the apical surface of some type II pneumocytes in the pulmonary sarcoidosis specimens, but it was completely masked by sialic acids in the nonpulmonary sarcoidosis specimens and in the normal lung tissues. Conclusions In pulmonary sarcoidosis, type II pneumocytes proliferated and the antigenicity of the surface membrane was altered. It is suggested that these type II pneumocytes may be vulnerable to injury by natural anti-TF antibodies that are cytotoxic when present with complement. This damage may decrease alveolar surfactant and cause focal alveolar collapse proceeding to pulmonary fibrosis in some cases of pulmonary sarcoidosis. |
| Databáze: | OpenAIRE |
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