M. Gharaeekermani et Sh. Phan, THE ROLE OF EOSINOPHILS IN PULMONARY FIBROSIS (REVIEW), INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 1(1), 1998, pp. 43-53
Pulmonary fibrosis is commonly characterized by inflammation of the al
veolar wall, leading to derangement of normal alveolar architecture, a
nd interstitial as well as intraalveolar fibrosis. The process involve
s cellular interactions via a complex cytokine network and heightened
collagen gene expression with abnormal deposition in the lung. Recent
studies have identified a myriad of cytokines with potential roles in
pulmonary fibrosis. Based on in vivo antibody neutralization studies,
important roles for tumor necrosis alpha (TNF alpha), macrophage infla
mmatory protein 1 alpha (MIP-1 alpha) and transforming growth factor b
eta (TGF beta), have been established. The recent demonstration that t
he eosinophil is a major source for several of these key pro-fibrogeni
c cytokines during the early stages of fibrosis, strongly suggest a ro
le for the eosinophil in pulmonary fibrosis. In vitro, eosinophils can
elaborate factors capable of stimulating fibroblast proliferation, an
d their presence in lungs undergoing many forms of pulmonary fibrosis
has been well documented. Further support for a role for eosinophils i
n pulmonary fibrosis are suggested by clinical data showing a correlat
ion between lung eosinophil count and a poor prognosis and decreased r
esponsiveness to therapy. This review will focus on the recent finding
s, which suggest novel potential roles for the eosinophil in the patho
genesis of pulmonary fibrosis.