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Autoimmune encephalomyelitis and uveitis induced by T cell immunity to self β-synuclein
被引:35
作者:
Mor, F
[1
]
Quintana, F
[1
]
Mimran, A
[1
]
Cohen, IR
[1
]
机构:
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
关键词:
D O I:
10.4049/jimmunol.170.1.628
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
beta-synuclein is a neuronal protein that accumulates in the plaques that characterize neurodegenerative diseases such as Parkinson's and Alzheimer's diseases. It has been proposed that immunization to peptides of plaque-forming proteins might be used therapeutically to help dissociate pathogenic plaques in the brain. We now report that immunization of Lewis rats with a peptide from beta-synuclein resulted in acute paralytic encephalomyelitis and uveitis. T cell lines and clones reactive to the peptide adoptively transferred the disease to naive rats. Immunoblotting revealed the presence of beta-synuclein in heavy myelin, indicating that the expression of beta-synuclein is not confined to neurons. These results add beta-synuclein to the roster of encephalitogenic self Ags, point out the potential danger of therapeutic autoimmunization to beta-synuclein, and alert us to the unsuspected possibility that autoimmunity to beta-synuclein might play an inflammatory role in the pathogenesis of neurodegeneration.
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页码:628 / 634
页数:7
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