Tenascin is a hexameric extracellular matrix (ECM) glycoprotein which
has been demonstrated to have a temporal relationship with active scar
formation in adult tissues. We hypothesized that this ECM protein mig
ht therefore serve to identify areas of active scarring in lung biopsi
es from patients with cryptogenic fibrosing alveolitis (CFA). The dist
ribution of tenascin was examined in open lung biopsies from ten patie
nts with CFA, six patients with sarcoidosis, and six pulmonary resecti
on specimens from patients with no evidence of interstitial lung disea
se, using an immunohistochemical technique. Immunoreactive tenascin wa
s not identified in histologically normal control lung parenchyma and
was only focally found around large aggregates of granulomas in sarcoi
dosis. In the CFA, tenascin production was demonstrated in minimally d
amaged alveolar walls and areas of active disease but not in end-stage
scarred lung. There was considerable local heterogeneity of staining
within cases, which did not appear to relate to the density of the loc
al inflammatory infiltrate. Large plaques of tenascin were noted to be
particularly associated with hyperplastic type II alveolar epithelial
lining cells, which are recognized to produce fibrogenic cytokines. T
he examination of tenascin expression in open lung biopsies from patie
nts with CFA may be useful in assessing fibrogenic activity and may th
us provide additional prognostic information.