Autor: |
FUJIMORI, Yoshiaki, KATAOKA, Mikio, TADA, Shinya, TAKEHARA, Hideki, MATSUO, Kiyoshi, MIYAKE, Toshitsugu, OKAHARA, Masayuki, YAMADORI, Ichiro, TANIMOTO, Mitsune |
Předmět: |
|
Zdroj: |
Respirology; Mar2003, Vol. 8 Issue 1, p33-40, 8p |
Abstrakt: |
Objective: A variety of inflammatory cells accumulate in the lungs of patients with interstitial lung disease. The potential for IL-8 to be released from these cells into the lungs of patients with idiopathic interstitial pneumonia (IIP), interstitial pneumonia with collagen vascular disease (IP-CVD), sarcoidosis (SAR) and hypersensitivity pneumonitis (HP) was investigated. Methodology: IL-8 levels were assessed by enzyme-linked immunosorbent assay in BAL fluid and serum, and the expression of IL-8 in the lungs of these patients was evaluated by immunohistochemistry. Results: Serum IL-8 levels were significantly elevated in patients with IIP (P < 0.05) and SAR (P < 0.01). In BAL fluid, the IL-8 level was significantly higher in patients with IIP (P < 0.05), IP-CVD (P < 0.01), SAR (P < 0.01) and HP (P < 0.01). In several cases, IL-8 level correlated with neutrophil density. The IL-8 immunopositive cells were type II pulmonary epithelial cells and alveolar and interstitial macrophages in patients with IIP and IP-CVD. Conclusions: IL-8 is likely to be a key factor in the pathogenesis of fibrosis of the lung and in lung injury. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
|