O'Connor Richard A, Anderton Stephen M
University of Edinburgh, Institute of Immunology and Infection Research, School of Biological Sciences, Kings Buildings, West Mains Road, Edinburgh EH9 3JT UK.
J Neuroimmunol. 2008 Jan;193(1-2):1-11. doi: 10.1016/j.jneuroim.2007.11.016.
The role of T regulatory (Treg) cells expressing the forkhead box transcription factor 3 (foxp3) in the control of autoaggressive immune responses is the subject of intense investigation. Here we explore the contribution of these cells to the regulation of experimental autoimmune encephalomyelitis (EAE). Starting from a historical perspective, we review their roles in preventing spontaneous disease, in setting the threshold for activation of a pathogenic response and in critically mediating the natural recovery from EAE. Current uncertainties and controversies are discussed in regard to EAE and multiple sclerosis as well as the potential for Treg-targeted immunotherapy.
表达叉头框转录因子3(foxp3)的调节性T(Treg)细胞在控制自身攻击性免疫反应中的作用是深入研究的课题。在此,我们探讨这些细胞对实验性自身免疫性脑脊髓炎(EAE)调节的贡献。从历史角度出发,我们回顾它们在预防自发性疾病、设定致病性反应激活阈值以及在介导EAE自然恢复过程中的关键作用。讨论了当前关于EAE和多发性硬化的不确定性与争议,以及针对Treg的免疫治疗潜力。