作者: Milica Lazarević , Giuseppe Battaglia , Bojan Jevtić , Neda Djedovic , Valeria Bruno
关键词: Lymph node 、 Peripheral blood mononuclear cell 、 Central nervous system 、 Experimental autoimmune encephalomyelitis 、 Multiple sclerosis 、 Immune system 、 Cancer research 、 FOXP3 、 Antigen 、 Chemistry
摘要: The aim of this study was to examine the in vitro effects slow-releasing H2S donor GYY4137 on immune cells involved pathogenesis central nervous system (CNS) autoimmune disease, multiple sclerosis (MS). specifically potentiated TGF-β expression and production dendritic significantly reduced IFN-γ IL-17 lymph node spinal cord T obtained from mice immunized with CNS antigens. Both proportion FoxP3+ regulatory CD4+ cells, percentage IL-17+ were upon culturing GYY4137. Interestingly, peripheral blood mononuclear MS patients had a lower H2S-producing enzyme, 3-mercaptopyruvate-sulfurtransferase (MPST), comparison those healthy donors. A significant inverse correlation between MPST several pro-inflammatory factors also observed. Further studies relevance observed results for therapy are warranted.