Abstract
Idiopathic pulmonary fibrosis is a chronic devastating disease of unknown etiology.Notherapy is currently available.Agrowingbody of evidence supports the role of transforming growth factor (TGF)- β1 as the major player in the pathogenesis of the disease. However, attempts to control its expression and to improve the outcome of pulmonary fibrosis have been disappointing. We tested the hypothesis that TGF-β1 is the dominant factor in the acute and chronic phases of pulmonary fibrosis and developed short interfering (si) RNAsdirectedtowardmolecules implicated in the disease. This study developed novel sequences of siRNAs targeting the TGF-β1 gene and evaluated their therapeutic efficacy in two models of pulmonary fibrosis: a model induced by bleomycin and a novel model of the disease developed spontaneously in mice overexpressing the full length of human TGF-β1 in the lungs. Intrapulmonary delivery of aerosolized siRNAs of TGF-β1 with sequences common to humans and rodents significantly inhibited bleomycin-induced pulmonary fibrosis in the acute and chronic phases of the disease and in a dose-dependent manner. Aerosolized human-specific siRNA also efficiently inhibited pulmonary fibrosis, improvedlung function,andprolonged survival in human TGF-β1 transgenic mice. Mice showed no off-target effects after intratracheal administration of siRNA. These results suggest the applicability of these novel siRNAs as tools for treating pulmonary fibrosis in humans.
Original language | English (US) |
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Pages (from-to) | 397-406 |
Number of pages | 10 |
Journal | American journal of respiratory cell and molecular biology |
Volume | 46 |
Issue number | 3 |
DOIs | |
State | Published - Mar 1 2012 |
Keywords
- Growth factors
- Idiopathic pulmonary fibrosis
- RNA interference
ASJC Scopus subject areas
- Molecular Biology
- Pulmonary and Respiratory Medicine
- Clinical Biochemistry
- Cell Biology