muramidase has been researched along with Lung-Diseases--Interstitial* in 4 studies
1 review(s) available for muramidase and Lung-Diseases--Interstitial
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Elevated serum levels of lysozyme in desquamative interstitial pneumonia.
We present a case of desquamative interstitial pneumonia (DIP) with elevated serum levels of angiotensin-converting enzyme and lysozyme, which are often found in sarcoidosis. After steroid therapy, improvements in the lung opacity and the serum lysozyme level were observed. Retrospective evaluation of four additional DIP cases showed that four of the five cases studied had an elevated serum lysozyme level. In an immunohistochemical analysis of the lung specimens, increased expression of lysozyme were found in the neutrophils and the alveolar macrophages. Elevated levels of serum lysozyme can occur in diseases such as DIP in which the neutrophil and macrophage activity may affect a patient's pathological condition. Topics: Adrenal Cortex Hormones; Biomarkers; Biopsy, Needle; Bronchoalveolar Lavage Fluid; Diagnosis, Differential; Follow-Up Studies; Humans; Idiopathic Pulmonary Fibrosis; Immunohistochemistry; Lung Diseases, Interstitial; Macrophages; Male; Middle Aged; Muramidase; Neutrophils; Peptidyl-Dipeptidase A; Radiography, Thoracic; Risk Assessment; Sarcoidosis, Pulmonary; Severity of Illness Index; Tomography, X-Ray Computed | 2010 |
3 other study(ies) available for muramidase and Lung-Diseases--Interstitial
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Pulmonary sarcoidosis with usual interstitial pneumonia distributed predominantly in the lower lung fields.
Nodular and reticular opacities were detected in both lower lung fields of a 75-year-old man in 2000. Bronchoscopy revealed pulmonary sarcoidosis. In 2002, nodular and reticular opacities were shown in the right upper lobe, and video-assisted thoracoscopic surgery was performed. The histological findings revealed usual interstitial pneumonia (UIP)-like lesions, whereas non-caseous granulomas were not detected. In the present case of pulmonary sarcoidosis, nodular and reticular opacities were predominantly distributed in both lower lung fields, and the histological findings obtained by video-assisted thoracoscopic surgery showed UIP-like lesions. These findings may enlighten the assist in understanding of the process of development of pulmonary sarcoidosis. Topics: Aged; Antigens, Neoplasm; Bronchoalveolar Lavage Fluid; Glucocorticoids; Humans; Lung; Lung Diseases, Interstitial; Male; Mucin-1; Mucins; Muramidase; Peptidyl-Dipeptidase A; Prednisolone; Radiography; Sarcoidosis, Pulmonary; Thoracoscopy | 2006 |
Adenosine deaminase activity and lysozyme levels in bronchoalveolar lavage fluid in patients with pulmonary tuberculosis.
The estimations of adenosine deaminase (ADA) activity and lysozyme (LYS) levels in pleural fluid have been proved useful tools in the diagnosis of tuberculous pleural effusions. Little is known about their usefulness when estimated in bronchoalveolar lavage fluid (BALF).. To evaluate whether both ADA activity and LYS levels in BALF could be employed in the diagnosis of pulmonary tuberculosis, and especially in active but acid fast bacilli (AFB) smear negative cases.. ADA activity and LYS levels were determined in BALF and serum obtained on the same day in 28 patients with tuberculosis, 21 with interstitial lung diseases, 14 with lung cancer and 13 with infectious diseases.. Patients with pulmonary tuberculosis had significantly higher ADA activity in BALF than patients with non-tuberculous lung diseases (P < 0.001). High BALF ADA activity in pulmonary tuberculosis patients suggests increased local production. In contrast, in this group of patients BALF LYS levels were not significantly higher than in the other groups of patients, but were in the group with interstitial lung diseases.. BALF ADA activity seems to be a useful tool in the differentiation of tuberculosis from other lung diseases. Its estimation can be restricted to the detection of cases with AFB negative smears. Topics: Adenosine Deaminase; Bronchoalveolar Lavage Fluid; Carcinoma, Bronchogenic; Case-Control Studies; Clinical Enzyme Tests; Diagnosis, Differential; Female; Humans; Lung Diseases; Lung Diseases, Interstitial; Lung Neoplasms; Male; Middle Aged; Muramidase; Tuberculosis, Pulmonary | 1998 |
Hydrolytic enzyme of the alveolar macrophage in diffuse pulmonary interstitial disease.
Hydrolytic enzymes [acid phosphatase, beta-glucuronidase, beta-D-N-acetyl glucosaminidase (beta-D-NAGA), lysozyme and angiotensin-converting enzyme (ACE)] are the major constituents of alveolar macrophages (AM). These enzymes play a crucial role in the pathogenesis of interstitial lung diseases. Cell-associated activity of several enzymes in alveolar macrophages obtained from control subjects (n = 5) and patients suffering five representative types of interstitial pulmonary diseases [sarcoidosis (n = 10), extrinsic allergic alveolitis (n = 5), idiopathic pulmonary fibrosis (n = 5), neoplastic infiltration of the lung (n = 5) and Pneumocystis carinii pneumonia (n = 5)] were evaluated. Cells were obtained by bronchoalveolar lavage and isolated by Ficoll-Hypaque gradient. Enzymatic activity was assessed by standardized tests. Bronchoalveolar lavage (BAL) lymphocyte counts were significantly elevated in the patients with active sarcoidosis (median: 57%), allergic extrinsic alveolitis (median: 51%) and neoplastic infiltration (median: 31%) as compared with the other groups, whereas BAL neutrophil and eosinophil counts were significantly elevated in the patients with idiopathic pulmonary fibrosis (neutrophil median: 29%; eosinophil median: 3%). The highest alveolar macrophage enzymatic activities were obtained in the active sarcoidosis group (median ACE: 23.38 microKat 10(-6) AM; median lysozyme: 8.64 nKat 10(-6) AM; median beta-glucuronidase: 324.22 U 10(-6) AM; median acid phosphatase: 0.78 nKat 10(-6) AM; median beta-D-NAGA: 1.85 nKat 10(-6) AM) which was significantly greater than in the control group (median ACE: 6.69 microKat 10(-6) AM; median lysozyme: 1.95 nKat 10(-6) AM; median beta-glucuronidase: 39.88 U 10(-6) AM; median acid phosphatase: 0.38 nKat 10(-6) AM; median beta-D-NAGA: 0.44 nKat 10(-6) AM). However, intracellular lysosomal enzymatic activities of alveolar macrophages from patients with allergic extrinsic alveolitis, a disease in which the degree of alveolar macrophage activation is maximal, were similar to those of the control group. These findings demonstrated a different pattern of expression of alveolar macrophage's hydrolytic enzymes in lymphocytic diffuse pulmonary interstitial disease. In sarcoidotic patients, hydrolytic enzymes were increased whereas in allergic extrinsic alveolitis, hydrolytic enzyme activities were similar to control groups. Indirect data suggest that the release of lysosomal enzymes by alveolar macrophages during Topics: Acetylglucosaminidase; Acid Phosphatase; Aged; Bronchoalveolar Lavage Fluid; Cell Count; Female; Glucuronidase; Humans; Hydrolases; Lung Diseases, Interstitial; Macrophages, Alveolar; Male; Middle Aged; Muramidase; Peptidyl-Dipeptidase A | 1996 |