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首页> 外文期刊>Journal of Neuroimmunology: Official Bulletin of the Research Committee on Neuroimmunology of the World Federation of Neurology >Therapeutic potential of atorvastatin-modified dendritic cells in experimental autoimmune neuritis by decreased Th1/Th17 cytokines and up-regulated T regulatory cells and NKR-P1+ cells
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Therapeutic potential of atorvastatin-modified dendritic cells in experimental autoimmune neuritis by decreased Th1/Th17 cytokines and up-regulated T regulatory cells and NKR-P1+ cells

机译:Th1 / Th17细胞因子减少以及T调节细胞和NKR-P1 +细胞上调,阿托伐他汀修饰的树突状细胞在实验性自身免疫性神经炎中的治疗潜力

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摘要

Statins have pleiotropic effects which include anti-inflammatory and immunomodulatory effects. In the present study, dendritic cells treated with atorvastatin (statin-DCs) could be induced into tolerogenic DCs. Administration of these tolerogenic DCs ameliorated clinical symptoms in experimental autoimmune neuritis (EAN), which was associated with reduced number of inflammatory cells in sciatic nerves, inhibited CD4+ T cells proliferation, down-regulated expression of co-stimulatory molecules (CD80 and CD86) and MHC class II, decreased levels of IFN-γ, TNF-α and IL-17A, increased number of NKR-P1+ cells (including NK and NKT cells), up-regulated number of Treg cells in lymph node MNC as well as increased Foxp3 expression in the thymus. These data indicated that statin-DCs could develop as a new therapeutic strategy to GBS in the future.
机译:他汀类药物具有多效作用,包括抗炎和免疫调节作用。在本研究中,可以将用阿托伐他汀(statin-DC)处理的树突状细胞诱导为致耐受性DC。这些致耐受性DC的施用改善了实验性自身免疫性神经炎(EAN)的临床症状,这与坐骨神经炎性细胞数量减少,抑制CD4 + T细胞增殖,共刺激分子(CD80和CD86)表达下调以及II类MHC,IFN-γ,TNF-α和IL-17A的水平降低,NKR-P1 +细胞(包括NK和NKT细胞)数量增加,淋巴结MNC中Treg细胞数量上调以及Foxp3升高在胸腺中表达。这些数据表明,他汀类药物DCs可能会在未来发展为GBS的新治疗策略。

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