Macrophage colony-stimulating factor (M-CSF) is a critical cytokine in the development of monocytic lineage and may have immunoregulatory properties. Here we show that peritoneal antigen presenting cells (APCs) treated with M-CSF produced decreased levels of proinflammatory cytokines IFN-gamma, TNF-alpha and IL-12. These APCs treated with M-CSF+autoantigen peptide significantly suppressed antigen-specific T cell proliferation, induced regulatory CD4(+) and CD8(+) T cells in vitro and in vivo, and significantly suppressed experimental autoimmune encephalomyelitis (EAE). Thus, in vitro treatment of APCs with M-CSF+autoantigen can be a novel therapeutic option for autoimmune diseases.
Antigen presenting cells treated in vitro by macrophage colony-stimulating factor and autoantigen protect mice from autoimmunity.
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作者:Guan Yangtai, Yu Shuo, Zhao Zhao, Ciric Bogoljub, Zhang Guang-Xian, Rostami Abdolmohamad
| 期刊: | Journal of Neuroimmunology | 影响因子: | 2.500 |
| 时间: | 2007 | 起止号: | 2007 Dec;192(1-2):68-78 |
| doi: | 10.1016/j.jneuroim.2007.09.021 | ||
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