Passage of amyloid β protein antibody across the blood-brain barrier in a mouse model of Alzheimer's disease

被引:159
作者
Banks, WA [1 ]
Terrell, B
Farr, SA
Robinson, SA
Nonaka, N
Morley, JE
机构
[1] Vet Affairs Med Ctr, Dept Internal Med, Div Geriatr, GRECC, St Louis, MO 63125 USA
[2] St Louis Univ, Sch Med, St Louis, MO 63106 USA
[3] Showa Univ, Sch Dent, Dept Oral Anat, Tokyo 142, Japan
[4] Showa Univ, Sch Med, Dept Anat 1, Tokyo 142, Japan
关键词
Alzheimer's disease; amyloid beta protein; amyloid precursor protein; antibody; blood-brain barrier; mice;
D O I
10.1016/S0196-9781(02)00261-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vaccinations against amyloid beta protein (AbetaP) reduce amyloid deposition and reverse learning and memory deficits in mouse models of Alzheimer's disease. This has raised the question of whether circulating antibodies, normally restricted by the blood-brain barrier (BBB), can enter the brain [Nat. Med. 7 (2001) 369-372]. Here, we show that antibody directed against AbetaP does cross the BBB at a very low rate. Entry is by way of the extracellular pathways with about 0.11% of an intravenous (i.v.) dose entering the brain by 1 h. Clearance of antibody from brain increasingly dominates over time, but antibody is still detectable in brain 72 h after i.v. injection. Uptake and clearance is not altered in mice overexpressing AbetaP. This ability to enter and exit the brain even in the presence of increased brain ligand supports the use of antibody in the treatment of Alzheimer's and other diseases of the brain. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:2223 / 2226
页数:4
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