TY - JOUR
T1 - Autoimmune encephalomyelitis and uveitis induced by T cell immunity to self β-synuclein
AU - Mor, Felix
AU - Quintana, Francisco
AU - Mimran, Avishai
AU - Cohen, Irun R.
PY - 2003/1/1
Y1 - 2003/1/1
N2 - β-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 β-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 β-synuclein in heavy myelin, indicating that the expression of β-synuclein is not confined to neurons. These results add β-synuclein to the roster of encephalitogenic self Ags, point out the potential danger of therapeutic autoimmunization to β-synuclein, and alert us to the unsuspected possibility that autoimmunity to β-synuclein might play an inflammatory role in the pathogenesis of neurodegeneration.
AB - β-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 β-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 β-synuclein in heavy myelin, indicating that the expression of β-synuclein is not confined to neurons. These results add β-synuclein to the roster of encephalitogenic self Ags, point out the potential danger of therapeutic autoimmunization to β-synuclein, and alert us to the unsuspected possibility that autoimmunity to β-synuclein might play an inflammatory role in the pathogenesis of neurodegeneration.
UR - http://www.scopus.com/inward/record.url?scp=0037218641&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.170.1.628
DO - 10.4049/jimmunol.170.1.628
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C2 - 12496452
AN - SCOPUS:0037218641
SN - 0022-1767
VL - 170
SP - 628
EP - 634
JO - Journal of Immunology
JF - Journal of Immunology
IS - 1
ER -