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Differential dose effects of recombinant IL-25 on the development of dextran sulfate sodium-induced colitis

OBJECTIVE: We evaluated different dose effects of rIL-25 on acute ulcerative colitis. MATERIALS AND METHODS: Mice were fed 2.5% dextran sulfate sodium (DSS) for 5 days while infused i.p. with repeated doses of rIL-25 (0.2, 0.4 and 0.8 μg) in PBS or PBS only after every 24 h at the same time as the s...

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Detalles Bibliográficos
Autores principales: Salum Mchenga, S. S., Wang, D., Janneh, F. M., Feng, Y., Zhang, P., Li, Z., Lu, C.
Formato: Texto
Lenguaje:English
Publicado: SP Birkhäuser Verlag Basel 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933846/
https://www.ncbi.nlm.nih.gov/pubmed/20490892
http://dx.doi.org/10.1007/s00011-010-0200-x
Descripción
Sumario:OBJECTIVE: We evaluated different dose effects of rIL-25 on acute ulcerative colitis. MATERIALS AND METHODS: Mice were fed 2.5% dextran sulfate sodium (DSS) for 5 days while infused i.p. with repeated doses of rIL-25 (0.2, 0.4 and 0.8 μg) in PBS or PBS only after every 24 h at the same time as the start of the DSS exposure. Clinical, macroscopical and microscopical assessment of colitis severity with survival study was performed. Colonic IL-25 expression and production of IFN-γ, IL-10 and IL-4 was also analyzed. RESULTS: At a dose of 0.2 μg, colitis was aggravated with high mortality, better improvements were observed at a dose of 0.4 μg, and colitis-induced diarrhea was reversed at a dose of 0.8 μg. The expression of IL-25 was found to decrease in severe colitis. Moreover, IL-25 inhibited production of mucosal IFN-γ, induced increase in IL-10 but not IL-4. CONCLUSION: Improvements in DSS-induced colitis in response to IL-25 suggest IL-25's protective role by mechanisms including inhibition of IFN-γ with enhancement of anti-inflammatory release.