共 20 条
Passive Immunization against Pyroglutamate-3 Amyloid-β Reduces Plaque Burden in Alzheimer-Like Transgenic Mice: A Pilot Study
被引:64
作者:

Frost, Jeffrey L.
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机构:
Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA

Liu, Bin
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Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA

Kleinschmidt, Martin
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h-index: 0
机构:
Probiodrug AG, Halle, Saale, Germany Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA

Schilling, Stephan
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h-index: 0
机构:
Probiodrug AG, Halle, Saale, Germany Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA

Demuth, Hans-Ulrich
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机构:
Probiodrug AG, Halle, Saale, Germany Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA

Lemere, Cynthia A.
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h-index: 0
机构:
Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA
[2] Probiodrug AG, Halle, Saale, Germany
关键词:
Alzheimer's disease;
Pyroglutamate-3;
amyloid-beta;
Monoclonal antibody;
Immunotherapy;
Transgenic mice;
A-BETA;
DISEASE;
DEPOSITION;
PEPTIDES;
MUTATION;
D O I:
10.1159/000335913
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background: N-terminally truncated and modified pyroglutamate-3 amyloid-beta protein (pE3-A beta) is present in most, if not all, cerebral plaque and vascular amyloid deposits in human Alzheimer's disease (AD). pE3-A beta deposition is also found in AD-like transgenic (tg) mouse brain, albeit in lesser quantities than general A beta. pE3-A beta resists degradation, is neurotoxic, and may act as a seed for A beta aggregation. Objective: We sought to determine if pE3-A beta removal by passive immunization with a highly specific monoclonal antibody (mAb) impacts pathogenesis in a mouse model of Alzheimer's amyloidosis. Methods: APPswe/PS1 Delta E9 tg mice were given weekly intraperitoneal injections of a new anti-pE3-A beta mAb (mAb07/1) or PBS from 5.8 to 13.8 months of age (prevention) or from 23 to 24.7 months of age (therapeutic). Multiple forms of cerebral A beta were quantified pathologically and biochemically. Gliosis and microhemorrhage were examined. Results: Chronic passive immunization with an anti-pE3-A beta mAb significantly reduced total plaque deposition and appeared to lower gliosis in the hippocampus and cerebellum in both the prevention and therapeutic studies. Insoluble A beta levels in hemibrain homogenates were not significantly different between immunized and control mice. Microhemorrhage was not observed with anti-pE3-A beta immunotherapy. Conclusions: Selective removal of pE3-A beta lowered general A beta plaque deposition suggesting a pro-aggregation or seeding role for pE3-A beta. Copyright (C) 2012 S. Karger AG, Basel
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页码:265 / 270
页数:6
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