Department of Clinical Neurosciences, Division of Neurology, Unit of Neuroimmunology and Multiple Sclerosis, University Hospital of Geneva and Faculty of Medicine, Geneva, Switzerland; Department of Pathology and Immunology, Faculty of Medicine, University of Geneva, Switzerland.
Department of Clinical Neurosciences, Division of Neurology, Unit of Neuroimmunology and Multiple Sclerosis, University Hospital of Geneva and Faculty of Medicine, Geneva, Switzerland.
J Neuroimmunol. 2014 Feb 15;267(1-2):105-10. doi: 10.1016/j.jneuroim.2013.12.004. Epub 2013 Dec 11.
Hepatocyte growth factor (HGF) limits mouse autoimmune neuroinflammation by promoting the development of tolerogenic dendritic cells (DCs). Given the role played by DCs in the establishment of immunological tolerance, agents that coerce DCs to adopt a protolerogenic function are currently under investigation for multiple sclerosis (MS) therapy. Here, we studied the immunomodulatory effects of HGF on DCs derived from human monocytes. DCs differentiated in the presence of HGF adopt a protolerogenic phenotype with increased ability to generate regulatory T cells, a property that might be exploited therapeutically in T cell-mediated immune disorders such as MS.
肝细胞生长因子 (HGF) 通过促进耐受原性树突状细胞 (DC) 的发育来限制小鼠自身免疫性神经炎症。鉴于 DC 在建立免疫耐受中的作用,目前正在研究促使 DC 采用耐受原性功能的药物,以用于多发性硬化症 (MS) 的治疗。在这里,我们研究了 HGF 对来源于人单核细胞的 DC 的免疫调节作用。在 HGF 存在的情况下分化的 DC 具有增加的产生调节性 T 细胞的能力,从而表现出耐受原性表型,这一特性可能在 T 细胞介导的免疫性疾病(如 MS)的治疗中得到利用。