کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6020284 | 1580401 | 2014 | 11 صفحه PDF | دانلود رایگان |
- Immunomodulator AS101 inhibited the differentiation of Th17 and Th1 cells.
- AS101 reduced the production of IL-17, GM-CSF, and IFN-γ in activated T cells.
- But AS101 promoted the production of IL-2 in activated T cells.
- AS101 blocked the activation of NFAT, Stat3, and RORγt, and increased activation of Erk1/2.
We reported that AS101 (organotellurium compound, trichloro(dioxoethylene-O,Oâ²) tellurate) inhibited the differentiation of Th17 cells and reduced the production of IL-17 and GM-CSF. In addition, AS101 promoted the production of IL-2 in activated T cells. Flow cytometric analysis showed that AS101 inhibited Th17 cell proliferation. AS101 blocked the activation of transcriptional factor NFAT, Stat3, and RORγt, and increased activation of Erk1/2, suggesting a mechanism of action of AS101. We further demonstrated that AS101 was effective in amelioration of experimental autoimmune encephalomyelitis (EAE), an animal model of multiple sclerosis. Finally, by real-time PCR analysis we showed that AS101 reduces the IL-17, IFN-γ, GM-CSF, and IL-6 mRNA expression in inflammatory cells of spinal cords. Additionally, flow cytometry analysis also indicated that the CD4 + T cells and IL-17 and GM-CSF-producing cells were reduced in the spinal cords of AS101 treated mice compared to those treated with PBS.
Journal: Journal of Neuroimmunology - Volume 273, Issues 1â2, 15 August 2014, Pages 31-41