The Diversity of Encephalitogenic CD4+ T Cells in Multiple Sclerosis and Its Animal Models

被引:45
|
作者
Segal, Benjamin M. [1 ,2 ]
机构
[1] Univ Michigan, Dept Neurol, Holtom Garrett Multiple Sclerosis Ctr, Ann Arbor, MI 48109 USA
[2] Ann Arbor VA Healthcare Syst, Neurol Serv, Ann Arbor, MI 48105 USA
关键词
Multiple Sclerosis; experimental autoimmune encephalomyelitis; T-helper cells; cytokines; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; CENTRAL-NERVOUS-SYSTEM; MYELIN BASIC-PROTEIN; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; PLACEBO-CONTROLLED TRIAL; INDUCE EAE; LESION LOCALIZATION; PROTEOLIPID PROTEIN; INTERFERON BETA-1A; IMMUNE DEVIATION;
D O I
10.3390/jcm8010120
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autoreactive CD4+ T cells, which target antigens in central nervous system (CNS) myelin, are widely believed to play a critical role in the pathogenesis of multiple sclerosis (MS) in concert with other immune effectors. This theory is supported by data from animal model experiments, genome-wide association studies, and immune profiles of individuals with MS. Furthermore, disease modifying agents that target lymphocytes significantly reduce the rate of MS clinical exacerbations. However, the properties of myelin-reactive CD4+ T cells that are critical for their pathogenic activities are not understood completely. This article reviews the literature on encephalitogenic CD4+ T cells, with an emphasis on T-helper (Th) lineage and cytokine production. An increased understanding of the spectrum of encephalitogenic T cells and how they differ from protective subsets is necessary for the development of the next generation of more effective and safer immunomodulatory therapies customized for individuals with MS and related disorders.
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页数:13
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