Abstract

BackgroundIt is difficult to predict survival in patients with idiopathic pulmonary fibrosis. Recently, several proteins, such as surfactant protein (SP) and KL-6, have been reported to be useful biologic markers for prediction of prognosis for interstitial pneumonias. It is not clear whether there is any relationship between expression of these proteins in regenerative/hyperplastic alveolar epithelial cells and prognosis of idiopathic interstitial pneumonias (IIPs).ObjectivesThis study aimed to elucidate the clinical significance of the expression of such lung secretory proteins as SP-A and KL-6 in lung tissues of patients with IIPs.MethodsWe retrospectively investigated the immunohistochemical expression of SP-A, KL-6, cytokeratin (CK), and epithelial membrane antigen (EMA) in alveolar epithelial cells in lung tissues obtained from surgical lung biopsy in 43 patients with IIPs, and analyzed the correlation between expression of these markers and the prognosis of each IIP patient. CK and EMA were used as general markers for epithelial cells.ResultsIn patients with usual interstitial pneumonia (UIP), the ratio of SP-A positive epithelial cells to all alveolar epithelial cells (SP-A positive ratio) in the collapsed and mural fibrosis areas varied, ranging from cases where almost all alveolar epithelial cells expressed SP-A to cases where only a few did. On the other hand, in many patients with nonspecific interstitial pneumonia (NSIP), many of the alveolar epithelial cells in the diseased areas expressed SP-A. The SP-A positive ratio was significantly lower in patients who died from progression of UIP than in patients with UIP who remained stable or deteriorated but did not die. In NSIP patients, a similar tendency was noted between the SP-A positive ratio and prognosis.ConclusionsThe results suggest that the paucity of immunohistochemical SP-A expression in alveolar epithelial cells in diseased areas (i.e. regenerative/hyperplastic alveolar epithelial cells) may predict a worse prognosis for patients with IIPs, especially patients with UIP. A prospective study is needed to confirm these results.

Highlights

  • It is difficult to predict survival in patients with idiopathic pulmonary fibrosis

  • We retrospectively investigated the immunohistochemical expression of surfactant protein (SP)-A, KL-6, cytokeratin (CK), and epithelial membrane antigen (EMA) in alveolar epithelial cells in lung tissues obtained from surgical lung biopsy in 43 patients with interstitial pneumonias (IIPs), and analyzed the correlation between expression of these markers and the prognosis of each IIP patient

  • The results suggest that the paucity of immunohistochemical surfactant apoprotein A (SP-A) expression in alveolar epithelial cells in diseased areas may predict a worse prognosis for patients with IIPs, especially patients with usual interstitial pneumonia (UIP)

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Summary

Introduction

It is difficult to predict survival in patients with idiopathic pulmonary fibrosis Several proteins, such as surfactant protein (SP) and KL-6, have been reported to be useful biologic markers for prediction of prognosis for interstitial pneumonias. It is not clear whether there is any relationship between expression of these proteins in regenerative/hyperplastic alveolar epithelial cells and prognosis of idiopathic interstitial pneumonias (IIPs). Several lung secretory proteins, such as surfactant protein (SP) and KL-6, were reported to be useful biologic markers for predicting prognosis of interstitial pneumonia (IP) [8,9,10,11,12,13,14]. It is not clear whether there is any relationship between expression of lung secretory proteins in regenerative/hyperplastic alveolar epithelium and prognosis in the subtypes of IIP

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