MPTP公司
神经退行性变
神经炎症
帕金森病
多巴胺能
黑质纹状体通路
免疫系统
神经科学
免疫学
黑质
调节性T细胞
T细胞
医学
白细胞介素2受体
生物
疾病
多巴胺
炎症
内科学
作者
Ashley D. Reynolds,David K. Stone,Jessica A. L. Hutter,Eric J. Benner,R. Lee Mosley,Howard E. Gendelman
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2010-01-30
卷期号:184 (5): 2261-2271
被引量:372
标识
DOI:10.4049/jimmunol.0901852
摘要
Nitrated alpha-synuclein (N-alpha-syn) immunization elicits adaptive immune responses to novel antigenic epitopes that exacerbate neuroinflammation and nigrostriatal degeneration in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model of Parkinson's disease. We show that such neuroimmune degenerative activities, in significant measure, are Th17 cell-mediated, with CD4(+)CD25(+) regulatory T cell (Treg) dysfunction seen among populations of N-alpha-syn-induced T cells. In contrast, purified vasoactive intestinal peptide induced and natural Tregs reversed N-alpha-syn T cell nigrostriatal degeneration. Combinations of adoptively transferred N-alpha-syn and vasoactive intestinal peptide immunocytes or natural Tregs administered to MPTP mice attenuated microglial inflammatory responses and led to robust nigrostriatal protection. Taken together, these results demonstrate Treg control of N-alpha-syn-induced neurodestructive immunity and, as such, provide a sound rationale for future Parkinson's disease immunization strategies.
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