T. Arai et al., Introduction of the interleukin-10 gene into mice inhibited bleomycin-induced lung injury in vivo, AM J P-LUNG, 278(5), 2000, pp. L914-L922
Citations number
48
Categorie Soggetti
da verificare
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
Interleukin (IL)-10 has been shown to reduce many inflammatory reactions. W
e investigated the in vivo effects of IL-10 on a bleomycin-induced lung inj
ury model. Hemagglutinating virus of Japan (HVJ)-liposomes containing a hum
an IL-10 expression vector (hIL10-HVJ) or a balanced salt solution as a con
trol (Cont-HVJ) was intraperitoneally injected into mice on day -3. This wa
s followed by intratracheal instillation of bleomycin (0.8 mg/kg) on day 0.
Myeloperoxidase activity of bronchoalveolar lavage fluid and tumor necrosi
s factor-alpha mRNA expression in bronchoalveolar lavage fluid cells on day
7 and hydroxyproline content of the whole lung on day 21 were inhibited si
gnificantly by hIL10-HVJ treatment. However, Cont-HVJ treatment could not s
uppress any of these parameters. We also examined the in vitro effects of I
L-10 on the human lung fibroblast cell line WI-38. IL-10 significantly redu
ced constitutive and transforming growth factor-beta-stimulated type I coll
agen mRNA expression. However, IL-10 did not affect the proliferation of WI
-38 cells induced by platelet-derived growth factor. These data suggested t
hat exogenous IL-10 may be useful in the treatment of pulmonary fibrosis.