Department of Surgery, University of Alberta, Edmonton, Alberta, Canada.
Cell Immunol. 2012 Nov;280(1):10-5. doi: 10.1016/j.cellimm.2012.11.004. Epub 2012 Nov 27.
One of the auto-antigens aberrantly targeted in Multiple sclerosis is myelin basic protein (MBP). In this study, chronic progressive multiple sclerosis (CPMS) patients receiving the experimental drug MBP8298, on a compassionate care trial, were examined before and after high dose peptide treatment for their circulating regulatory T-cell numbers and their responses to the common mitogens, phytohemagglutinin and poke-weed mitogen. Peripheral blood mononuclear cells (PBMCs) isolated from these patients before treatment displayed anergy upon stimulation with phytohemagglutinin; measured through reduced proliferation, IFN-γ and IL-17A secretion in an in vitro cell culture system. 6 Weeks and 6months after treatment their PBMCs displayed a reversal of anergy with phytohemagglutinin stimulation. There was also a marked increase in their CD4(+)CD25(+hi)FoxP3(+) T-cells regulatory T-cells. These results suggest that high dose MBP8298 treatment has a profound effect on the circulating T-cells of CPMS patients, capable of reversing peripheral anergy and establishing T regulation.
在多发性硬化症中,异常靶向的自身抗原之一是髓鞘碱性蛋白(MBP)。在这项研究中,接受实验药物 MBP8298 进行同情治疗的慢性进行性多发性硬化症(CPMS)患者,在接受高剂量肽治疗前后,对其循环调节性 T 细胞数量及其对常见有丝分裂原植物血凝素和美洲商陆丝裂原的反应进行了检查。治疗前从这些患者中分离出的外周血单核细胞(PBMC)在用植物血凝素刺激时表现出无反应性;通过体外细胞培养系统测量增殖减少、IFN-γ 和 IL-17A 的分泌。治疗后 6 周和 6 个月,其 PBMC 对植物血凝素刺激的无反应性逆转。其 CD4(+)CD25(+hi)FoxP3(+)T 细胞调节性 T 细胞也明显增加。这些结果表明,高剂量 MBP8298 治疗对 CPMS 患者的循环 T 细胞有深远影响,能够逆转外周无反应性并建立 T 调节。