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- W2105124776 abstract "<b>Backgroud:</b> Idiopathic pulmonary fibrosis is a devastating disorder for which there is no effective treatment. Transforming growth factor (TGF)-β plays a critical role in provoking fibrosis. Interleukin (IL)-10 is a potent immunosuppressive cytokine but its effect on the fibrosing process is unclear. A study was undertaken to examine whether IL-10 affects the production and activation of TGF-β and thus can attenuate the fibrosis. <b>Methods:</b> Mice were given an intratracheal injection of bleomycin. On day 1 or 14, IL-10 gene was delivered by rapid intravenous injection of Ringer’s solution containing plasmid. Two weeks after the plasmid injection the mice were examined for fibrosis. The effect of IL-10 on TGF-β production by alveolar macrophages was assessed. <b>Results:</b> Even when delivered during the fibrosing phase, IL-10 gene significantly suppressed the pathological findings, hydroxyproline content, and production of both active and total forms of TGF-β<sub>1</sub> in the lung. Immunohistochemical analyses showed that alveolar macrophages were one of the major sources of TGF-β<sub>1</sub> and IL-10 diminished the intensity of the staining. IL-10 also suppressed the expression of α<sub>V</sub>β<sub>6</sub> integrin, a molecule that plays an important role in TGF-β activation, on lung epithelial cells. Alveolar macrophages from bleomycin injected mice produced TGF-β<sub>1</sub> spontaneously ex vivo, which was significantly suppressed by treatment of the mice in vivo or by treatment of the explanted macrophages ex vivo with IL-10. <b>Conclusion:</b> IL-10 suppresses the production and activation of TGF-β in the lung and thus attenuates pulmonary fibrosis, even when delivered in the chronic phase." @default.
- W2105124776 created "2016-06-24" @default.
- W2105124776 creator A5081937545 @default.
- W2105124776 date "2006-10-01" @default.
- W2105124776 modified "2023-10-16" @default.
- W2105124776 title "In vivo IL-10 gene delivery attenuates bleomycin induced pulmonary fibrosis by inhibiting the production and activation of TGF- in the lung" @default.
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- W2105124776 doi "https://doi.org/10.1136/thx.2005.056317" @default.
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