Introduction of the interleukin-10 gene into mice inhibited bleomycin-induced lung injury in vivo

T Arai, KY Abe, H Matsuoka… - … of Physiology-Lung …, 2000 - journals.physiology.org
T Arai, KY Abe, H Matsuoka, M Yoshida, M Mori, S Goya, H Kida, K Nishino, T Osaki…
American Journal of Physiology-Lung Cellular and Molecular …, 2000journals.physiology.org
Interleukin (IL)-10 has been shown to reduce many inflammatory reactions. We investigated
the in vivo effects of IL-10 on a bleomycin-induced lung injury model. Hemagglutinating virus
of Japan (HVJ)-liposomes containing a human IL-10 expression vector (hIL10-HVJ) or a
balanced salt solution as a control (Cont-HVJ) was intraperitoneally injected into mice on
day− 3. This was followed by intratracheal instillation of bleomycin (0.8 mg/kg) on day 0.
Myeloperoxidase activity of bronchoalveolar lavage fluid and tumor necrosis factor-α mRNA …
Interleukin (IL)-10 has been shown to reduce many inflammatory reactions. We investigated the in vivo effects of IL-10 on a bleomycin-induced lung injury model. Hemagglutinating virus of Japan (HVJ)-liposomes containing a human IL-10 expression vector (hIL10-HVJ) or a balanced salt solution as a control (Cont-HVJ) was intraperitoneally injected into mice on day −3. This was followed by intratracheal instillation of bleomycin (0.8 mg/kg) onday 0. Myeloperoxidase activity of bronchoalveolar lavage fluid and tumor necrosis factor-α mRNA expression in bronchoalveolar lavage fluid cells on day 7 and hydroxyproline content of the whole lung on day 21 were inhibited significantly by hIL10-HVJ treatment. However, Cont-HVJ treatment could not suppress any of these parameters. We also examined the in vitro effects of IL-10 on the human lung fibroblast cell line WI-38. IL-10 significantly reduced constitutive and transforming growth factor-β-stimulated type I collagen mRNA expression. However, IL-10 did not affect the proliferation of WI-38 cells induced by platelet-derived growth factor. These data suggested that exogenous IL-10 may be useful in the treatment of pulmonary fibrosis.
American Physiological Society