PMID- 9216211 OWN - NLM STAT- MEDLINE DCOM- 19970923 LR - 20151119 IS - 0301-1542 (Print) IS - 0301-1542 (Linking) VI - 34 Suppl DP - 1996 Dec TI - [Role of alveolar macrophages in the pathogenesis of idiopathic interstitial pneumonia]. PG - 175-80 AB - To clarify role of alveolar macrophages in the pathogenesis of idiopathic interstitial pneumonia (IIP), we studied (1) the localization and expression of monocyte chemoattractant protein-1 (MCP-1) in IIP by immunohistochemistry and in situ hybridization. (2) the role of MCP-1 in macrophage recruitment to be lung, and (3) the clinical usefulness of measuring MCP-1. (1) In IIP, MCP-1 was observed in cuboidal and flattened metaplastic epithelial cells, alveolar macrophages, and vascular endothelial cells. In contrast, no epithelial cells from patients without IIP stained positive for MCP-1, although alveolar macrophages and vascular endothelial cells were labeled. MCP-1 production by epithelial cells in IIP may be caused by the metaplastic nature of the epithelial cells and may be a main cause of the irreversible progression of IIP. (2) MCP-1 levels in bronchoalveolar lavage fluid (BALF) were significantly higher in the IIP, the interstitial pneumonia due to collagen vascular disease (IP-CVD) and sarcoidosis groups than in normal controls. In the IIP group, the MCP-1 level was significantly higher than in any other patient groups. In all three groups of patients, the monocyte chemotactic activity in BALF correlated positively with the MCP-1 levels in BALF, and were neutralized by anti-MCP-1. (3) BALF MCP-1 levels were significantly higher than serum MCP-1 levels in the IIP group, and they were lower in the IP-CVD and non-specific interstitial pneumonia groups. Serum MCP-1 levels reflected the activity of interstitial lung diseases, especially during treatment with corticosteroids. These results indicate (1) that MCP-1 plays a significant role in the recruitment of monocytes into the lung in IIP, (2) that measuring MCP-1 levels both in BALF and in serum may help discriminate IIP from other types of interstitial lung diseases, and (3) that monitoring the serum MCP-1 level may be useful in estimating the activity of interstitial lung diseases. FAU - Suga, M AU - Suga M AD - First Department of Internal Medicine, Kumamoto University School of Medicine, Japan. FAU - Iyonaga, K AU - Iyonaga K FAU - Ando, M AU - Ando M LA - jpn PT - English Abstract PT - Journal Article PT - Review PL - Japan TA - Nihon Kyobu Shikkan Gakkai Zasshi JT - Nihon Kyobu Shikkan Gakkai zasshi JID - 7505737 RN - 0 (Biomarkers) RN - 0 (Chemokine CCL2) SB - IM MH - Biomarkers/analysis MH - Bronchoalveolar Lavage Fluid/chemistry MH - Chemokine CCL2/*physiology MH - Endothelium, Vascular/metabolism MH - Humans MH - Lung Diseases, Interstitial/*etiology MH - Macrophages, Alveolar/*physiology RF - 5 EDAT- 1996/12/01 00:00 MHDA- 1996/12/01 00:01 CRDT- 1996/12/01 00:00 PHST- 1996/12/01 00:00 [pubmed] PHST- 1996/12/01 00:01 [medline] PHST- 1996/12/01 00:00 [entrez] PST - ppublish SO - Nihon Kyobu Shikkan Gakkai Zasshi. 1996 Dec;34 Suppl:175-80.