FROM GRANULOMA TO FIBROSIS IN INTERSTITIAL LUNG-DISEASES - MOLECULAR AND CELLULAR INTERACTIONS

Citation
Jf. Mornex et al., FROM GRANULOMA TO FIBROSIS IN INTERSTITIAL LUNG-DISEASES - MOLECULAR AND CELLULAR INTERACTIONS, The European respiratory journal, 7(4), 1994, pp. 779-785
Citations number
92
Categorie Soggetti
Respiratory System
ISSN journal
09031936
Volume
7
Issue
4
Year of publication
1994
Pages
779 - 785
Database
ISI
SICI code
0903-1936(1994)7:4<779:FGTFII>2.0.ZU;2-2
Abstract
Granuloma is a feature of many chronic interstitial lung diseases, and may serve as a focus for subsequent fibrosis. Granulomas are composed of structured masses of cells of the macrophage lineage, which adopt an epithelioid aspect, interspersed with lymphocytes. They are formed around local centres of irritation. During their resolution fibroblast s congregate around the structures and may penetrate tile interior. In many cases, granulomas can disappear without leaving lasting traces. However, especially when damage has occurred to the surrounding tissue , permanent scarring and fibrosis may occur. Both types of cell presen t the granuloma are capable of secreting a number of factors influenci ng the accumulation and proliferation of fibroblasts, both positively and negatively. The possible roles played by the different factors and , especially, interactions between them are discussed in the light of fibrosis formation. Possible therapeutic interventions are summarized.