Generation and Therapeutic Efficacy of Highly Oligomer-Specific β-Amyloid Antibodies

被引:88
作者
Hillen, Heinz [1 ]
Barghorn, Stefan [1 ]
Striebinger, Andreas [1 ]
Labkovsky, Boris [2 ]
Mueller, Reinhold [1 ]
Nimmrich, Volker [1 ]
Nolte, Marc W. [1 ]
Perez-Cruz, Claudia [1 ]
van der Auwera, Ingrid [3 ]
van Leuven, Fred [4 ]
van Gaalen, Marcel [1 ]
Bespalov, Anton Y. [1 ]
Schoemaker, Hans [1 ]
Sullivan, James P. [5 ]
Ebert, Ulrich [1 ]
机构
[1] Global Pharmaceut Res & Dev, Neurosci Res, D-67061 Ludwigshafen, Germany
[2] Abbott BioRes Ctr, Worcester, MA 01605 USA
[3] ReMYND NV, BE-3001 Louvain, Belgium
[4] Katholieke Univ Leuven, Expt Genet Grp, BE-3000 Leuven, Belgium
[5] Global Pharmaceut Res & Dev, Neurosci Res, Abbott Pk, IL 60064 USA
关键词
LONG-TERM POTENTIATION; A-BETA; ALZHEIMERS-DISEASE; PRECURSOR PROTEIN; TRANSGENIC MICE; HIPPOCAMPAL-NEURONS; SYNAPSE LOSS; MEMORY; BRAIN; IMMUNIZATION;
D O I
10.1523/JNEUROSCI.5721-09.2010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oligomers of the beta-amyloid (A beta) peptide have been indicated in early neuropathologic changes in Alzheimer's disease. Here, we present a synthetic A beta(20-42) oligomer (named globulomer) with a different conformation to monomeric and fibrillar A beta peptide, enabling the generation of highly A beta oligomer-specific monoclonal antibodies. The globulomer-derived antibodies specifically detect oligomeric but not monomeric or fibrillar A beta in various A beta preparations. The globulomer-specific antibody A-887755 was able to prevent A beta oligomer binding and dynamin cleavage in primary hippocampal neurons and to reverse globulomer-induced reduced synaptic transmission. In amyloid precursor protein (APP) transgenic mice, vaccination with A beta globulomer and treatment with A-887755 improved novel object recognition. The cognitive improvement is likely attributable to reversing a deficit in hippocampal synaptic spine density in APP transgenic mice as observed after treatment with A-887755. Our findings demonstrate that selective reduction of A beta oligomers by immunotherapy is sufficient to normalize cognitive behavior and synaptic deficits in APP transgenic mice.
引用
收藏
页码:10369 / 10379
页数:11
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