Dobson C B, Itzhaki R F
Department of Optometry and Neuroscience, University of Manchester Institute of Science and Technology, United Kingdom.
Neurobiol Aging. 1999 Jul-Aug;20(4):457-65. doi: 10.1016/s0197-4580(99)00055-x.
Until recently, the only risk factors implicated in noninherited cases of Alzheimer's disease were increasing age, Down's syndrome, and probably, head injury. Having found that herpes simplex type 1 virus (HSV1) is present in the brain of many elderly people, we discovered that it is a risk factor for Alzheimer's disease when in the central nervous system of APOE-epsilon4 allele carriers. On the basis of this result and our finding that apoE-epsilon4 is a risk factor for herpes labialis, we suggested that the combination of virus and genetic factor is particularly damaging in the nervous system. The present review describes 1) the search for HSV1 in human brain; 2) HSV1 infection of the peripheral nervous system; 3) HSV1 infection of the central nervous system; 4) how APOE genotype might influence HSV1 infection; 5) possible APOE genotype effect on viral latency and its reactivation; 6) interactions of viruses with lipoproteins, their components, and lipoprotein receptors; 7) the role of APOE in repair; 8) pathological processes in AD and their relationship to prior damage; and 9) implications for the prevention or treatment of Alzheimer's disease.
直到最近,非遗传性阿尔茨海默病所涉及的唯一风险因素是年龄增长、唐氏综合征,可能还有头部损伤。在发现许多老年人的大脑中存在单纯疱疹病毒1型(HSV1)后,我们发现,对于携带APOE-ε4等位基因的人来说,当HSV1存在于其中枢神经系统时,它是阿尔茨海默病的一个风险因素。基于这一结果以及我们发现载脂蛋白E-ε4是唇疱疹的一个风险因素,我们提出病毒与遗传因素的结合对神经系统具有特别大的损害。本综述描述了:1)在人类大脑中寻找HSV1的过程;2)HSV1对外周神经系统的感染;3)HSV1对中枢神经系统的感染;4)APOE基因型可能如何影响HSV1感染;5)APOE基因型对病毒潜伏及其重新激活可能产生的影响;6)病毒与脂蛋白、其成分以及脂蛋白受体之间的相互作用;7)载脂蛋白E在修复中的作用;8)阿尔茨海默病中的病理过程及其与先前损伤的关系;9)对阿尔茨海默病预防或治疗的启示。