Multiple sclerosis immunology The healthy immune system vs the MS immune system

被引:129
作者
Kasper, Lloyd H. [1 ,2 ,3 ]
Shoemaker, Jennifer
机构
[1] Dartmouth Med Sch, Dartmouth Hitchcock Multiple Sclerosis Clin, Dept Neurol, Lebanon, NH 03756 USA
[2] Dartmouth Med Sch, Dartmouth Hitchcock Multiple Sclerosis Clin, Dept Med, Lebanon, NH 03756 USA
[3] Dartmouth Med Sch, Dartmouth Hitchcock Multiple Sclerosis Clin, Dept Microbiol Immunol, Lebanon, NH 03756 USA
关键词
REGULATORY T-CELLS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MYELIN BASIC-PROTEIN; DENDRITIC CELLS; PHASE-II; DOUBLE-BLIND; TH17; CELLS; OPEN-LABEL; B-CELLS; OSTEOPONTIN;
D O I
10.1212/WNL.0b013e3181c97c8f
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple sclerosis (MS) is a debilitating autoimmune disease characterized by both inflammation and axonal degeneration. The resulting demyelination and subsequent degeneration of axons account for the disability of patients with MS. Early investigations indicated that disease progression was driven by CD4(+) effector T cells. However, clinical therapies specifically targeting these cells have, for the most part, not been effective. Therefore, new areas of research in experimental autoimmune encephalomyelitis (the experimental model of MS) and human MS have identified previously unknown contributions to disease pathogenesis, including interleukin-17-producing T helper 17 cells, B cells, CD8(+) T cells, and both CD4(+) and CD8(+) T-regulatory cells. Research into the respective mechanisms of action of these cells has identified novel therapeutic targets to combat this devastating disease. This article reviews the autoimmune response in patients with MS compared with individuals without MS and summarizes the fundamental differences in the immunologic response between people with and without MS. Investigations into these autoimmune differences and the disruption of the homeostatic balance of the immune system will help guide future research into MS therapeutics, with particular attention to the long-term management of this disease. NEUROLOGY 2010;74(Suppl1):S2-S8
引用
收藏
页码:S2 / S8
页数:7
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