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Passive Immunization Reduces Behavioral and Neuropathological Deficits in an Alpha-Synuclein Transgenic Model of Lewy Body Disease
Author(s) -
Eliezer Masliah,
Edward Rockenstein,
Michael Mante,
Leslie Crews,
Brian Spencer,
Anthony Adame,
Christina Patrick,
Margarita Trejo,
Kiren Ubhi,
Troy T. Rohn,
Sarah Mueller-Steiner,
Peter Seubert,
Robin Barbour,
Lisa McConlogue,
Manuel Buttini,
Dora Games,
Dale Schenk
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0019338
Subject(s) - dementia with lewy bodies , alpha synuclein , parkinson's disease , monoclonal antibody , neuroscience , lewy body , genetically modified mouse , synucleinopathies , immunization , in vivo , medicine , antibody , biology , dementia , transgene , immunology , disease , pathology , genetics , gene
Dementia with Lewy bodies (DLB) and Parkinson's Disease (PD) are common causes of motor and cognitive deficits and are associated with the abnormal accumulation of alpha-synuclein (α-syn). This study investigated whether passive immunization with a novel monoclonal α-syn antibody (9E4) against the C-terminus (CT) of α-syn was able to cross into the CNS and ameliorate the deficits associated with α-syn accumulation. In this study we demonstrate that 9E4 was effective at reducing behavioral deficits in the water maze, moreover, immunization with 9E4 reduced the accumulation of calpain-cleaved α-syn in axons and synapses and the associated neurodegenerative deficits. In vivo studies demonstrated that 9E4 traffics into the CNS, binds to cells that display α-syn accumulation and promotes α-syn clearance via the lysosomal pathway. These results suggest that passive immunization with monoclonal antibodies against the CT of α-syn may be of therapeutic relevance in patients with PD and DLB.

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