Infiltration of the brain by pathogens causes Alzheimer's disease

被引:142
作者
Itzhaki, RE [1 ]
Wozniak, MA
Appelt, DM
Balin, B
机构
[1] Univ Manchester, Inst Sci & Technol, UMIST, Dept Optometry & Neurosci,Mol Neurobiol Lab, Manchester M60 1QD, Lancs, England
[2] Philadelphia Coll Osteopath Med, Dept Biomed Sci, Philadelphia, PA 19131 USA
[3] Philadelphia Coll Osteopath Med, Dept Pathol Microbiol & Immunol, Philadelphia, PA 19131 USA
关键词
Alzheimer's disease; herpes simplex virus type 1; apolipoprotein E; Chlamydia pneumoniae; polymerase chain reaction; intrathecal antibodies; human herpesvirus 6; human cytomegalovirus; blood-brain barrier; olfactory pathways; chronic inflammation; animal model;
D O I
10.1016/j.neurobiolaging.2003.12.021
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Despite very numerous studies on Alzheimer's disease (AD), especially on amyloid plaques and neurofibrillary tangles, little information has been obtained thus on the causes of the disease. Evidence is described here that implicates firstly herpes simplex virus type I (HSV1) as a strong risk factor when it is present in brain of carriers of the type 4 allele of the gene for apolipoprotein E (APOE-epsilon4). Indirect support comes from studies indicating the role of APOE in several diverse diseases of known pathogen cause. A second putative risk factor is the bacterium, Chlamydia pneumoniae. This pathogen has been identified and localized in AD brain. Current studies aimed at "proof of principle" address the entry of the organism into the CNS, the neuroinflammatory response to the organism, and the role that the organism plays in triggering AD pathology. An infection-based animal model demonstrates that following intranasal inoculation of BALB/c mice with C. pneumoniae, amyloid plaques/deposits consistent with those observed in the AD brain develop, thus implicating this infection in the etiology of AD. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:619 / 627
页数:9
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