TENASCIN IMMUNOREACTIVITY AS A PROGNOSTIC MARKER IN USUAL INTERSTITIAL PNEUMONIA

Citation
R. Kaarteenahowiik et al., TENASCIN IMMUNOREACTIVITY AS A PROGNOSTIC MARKER IN USUAL INTERSTITIAL PNEUMONIA, American journal of respiratory and critical care medicine, 154(2), 1996, pp. 511-518
Citations number
35
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
ISSN journal
1073449X
Volume
154
Issue
2
Year of publication
1996
Pages
511 - 518
Database
ISI
SICI code
1073-449X(1996)154:2<511:TIAAPM>2.0.ZU;2-X
Abstract
In this investigation, tenascin (Tn) expression was studied in 51 case s of different types of fibrotic lung disorders originating for years 1981 to 1995. Our aim was to test if accumulation of Tn at the site of lung injury in usual interstitial pneumonia (UIP) could correlate wit h the prognosis. Lung biopsies taken from 28 patients with UIP, six wi th desquamative interstitial pneumonia (DIP), six with sarcoidosis, fi ve with extrinsic allergic bronchioloalveolitis, five with bronchiolit is obliterans organizing pneumonia (BOOP), and one with nonspecific in terstitial pneumonia were studied for the expression of Tn by using an immunohistochemical technique. In addition to Tn immunohistochemistry , selected cases were also studied by immunoelectron microscopy and We stern blotting. For prognostic studies in UIP the clinical follow-up i nformation was obtained from the patient records. The expression of Tn was increased in each type of fibrosis, especially in UIP. In immunoe lectron microscopy the most prominent labeling in UIP was found in ass ociation with collagen fibers and within the type 2 pneumocytes. Every studied case of UIP showed reactivity for a polypeptide of M(r) appro ximate to 200,000 by Western blotting. In patients with UIP, increased Tn expression, especially under metaplastic bronchiolar-type epitheli um, was associated with a shortened survival time. Immunoelectron micr oscopic findings support the idea that Tn in UIP is synthesized by the regenerating epithelial rather than interstitial cells in response to pulmonary interstitial inflammation.