Peripheral and central biodistribution of 111In-labeled anti-beta-amyloid autoantibodies in a transgenic mouse model of Alzheimer's disease

被引：29

作者：

Bacher, Michael ^{[1
]}

Depboylu, Candan ^{[1
]}

Du, Yansheng ^{[3
]}

Noelker, Carmen ^{[1
]}

Oertel, Wolfgang H. ^{[1
]}

Behr, Thomas ^{[2
]}

Henriksen, Gjermund ^{[4
]}

Behe, Martin ^{[2
]}

Dodel, Richard ^{[1
]}

机构：

[1] Univ Marburg, Dept Neurol, D-35033 Marburg, Germany

[2] Univ Marburg, Dept Nucl Med, D-35033 Marburg, Germany

[3] Indiana Univ, Sch Med, Dept Neurol, Indianapolis, IN 46202 USA

[4] Tech Univ Munich, Dept Nucl Med, Munich, Germany

来源：

NEUROSCIENCE LETTERS | 2009年 / 449卷 / 03期

关键词：

Alzheimer's disease; beta-Amyloid; Passive immunization; Naturally occurring autoantibodies; Blood-brain barrier; BLOOD-BRAIN-BARRIER; HUMAN-ANTIBODIES; IN-VIVO; PEPTIDE; IMMUNIZATION; VACCINATION; PATHOLOGY; BURDEN; IMMUNOTHERAPY; MECHANISMS;

D O I：

10.1016/j.neulet.2008.08.083

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

Active as well as passive immunization against beta-amlyoid (A beta) has been proposed as a treatment to lower cerebral amyloid burden and stabilize cognitive decline in Alzheimer's disease (AD). To clarify the mechanism of action underlying passive immunization, the in vivo distribution (and sites of degradation) of peripherally administered radiolabeled human and mouse anti-A beta antibodies were analyzed in a transgenic mouse model of AD. In APP23 mice, a model in which mutated human amyloid precursor protein is overexpressed, the biodistribution of intravenously applicated (111)indium-conjugated affinity-purified human polyclonal autoantibodies (NAbs-A beta) was compared to that of monoclonal anti-AP(1-17) (6E10), anti-A beta(17-24) antibodies (4G8) and anti-CD-20 (Rituximab), a non-A beta targeting control. Blood clearance half-lives were 50 +/- 6 h for Rituximab, 20-30 h for NAbs-A beta, 29 +/- 5 h for 4G8 and 27 +/- 3 h for 6E10. Blood activity was higher for 6E10 at 4h as compared to 4GS, Rituximab and NAbs-A beta. At the 96 h time point, Rituximab had the highest blood activity among the antibodies tested. As expected, all antibodies displayed hepatobiliary clearance. Additionally, NAbs-A beta was excreted in the urinary tract. Liver and kidney uptake of NAbs-A beta increased over time and was higher than in the monoclonal antibodies at 48 h/96 h. The brain-to-blood radioactivity ratio for NAbs-A beta at later time points (> 48 h) was higher than that of 6E10, 4G8 and Rituximab. In addition, the distribution varied, with highest values found in the hippocampus. Our data indicate a cerebral accumulation of human NAbs-A beta in the APP23 model. Further studies with human immunoglobulins and particularly with those that recognize different A beta-epitopes are required in order to delineate in more detail the mode of action of NAbs-A beta. (c) 2008 Elsevier Ireland Ltd. All rights reserved.

引用

页码：240 / 245

页数：6

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