A. Emad et Gr. Rezaian, Immunoglobulins and cellular constituents of the BAL fluid of patients with sulfur mustard gas-induced pulmonary fibrosis, CHEST, 115(5), 1999, pp. 1346-1351
Citations number
27
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Study objective: The acute heavy exposure to sulfur mustard gas can lead to
pulmonary fibrosis (PF), This study was performed to determine the cellula
r and protein content of BAL fluid in 24 patients with sulfur mustard gas-i
nduced PF,
Patients: Twenty-four veterans with sulfur mustard gas-induced PF and 18 no
nexposed veterans serving as control subjects were enrolled into the study.
Measurements: Chest roentgenograms, pulmonary function tests (PFTs), tests
for carbon monoxide diffusing capacity of the lung (DLCO), high-resolution
CT scans of the chest, BAL via fiberoptic bronchoscopy, analyses of BAL flu
ids for cellular and protein constituents, and determinations of serum albu
min and Ig levels were performed in all eases. A transbronchial lung biopsy
was done in all patients following BAL,
Results: Neutrophilic alveolitis was the predominant feature. Neutrophils (
p = 0.0001) and eosinophils (p = 0.0001) were the predominant cell types in
the BAL fluid of patients with PF, There was a strong correlation between
the BAL fluid neutrophil count (rho = 0.76; p = 0.0003) or its percentage (
rho = 0.77; p = 0.0003) and the degree of fibrosis, Of the BAL fluid Ig lev
els, only the IgG level in the study group was significantly higher than th
e IgG level of the control group (p = 0.0001), Of the PFT physiologic param
eters, only the percentage of DLCO showed a significant correlation with th
e degree of fibrosis (rho = -0.76; p < 0.001).
Conclusion: The cellular constituents of BAL, fluid in patients with sulfur
mustard gas-induced PF are very similar to the cellular constituents seen
in patients with idiopathic PF, and this finding indicates the presence of
an ongoing active alveolitis in PF.