Herpesviruses in brain and Alzheimer's disease

被引:158
作者
Lin, WR [1 ]
Wozniak, MA
Cooper, RJ
Wilcock, GK
Itzhaki, RF
机构
[1] UMIST, Dept Optometry & Neurosci, Mol Neurobiol Lab, Manchester M60 1QD, Lancs, England
[2] Univ Manchester, Sch Med, Div Virol, Manchester, Lancs, England
[3] Frenchay Hosp, Dept Care Elderly, Bristol BS16 1LE, Avon, England
关键词
Alzheimer's disease; herpes simplex virus type 2; cytomegalovirus; human herpesvirus 6; polymerase chain reaction; brain;
D O I
10.1002/path.1127
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
It has been established, using polymerase chain reaction (PCR), that herpes simplex virus type 1 (HSV1) is present in a high proportion of brains of elderly normal subjects and Alzheimer's disease (AD) patients. It was subsequently discovered that the virus confers a strong risk of AD when in brain of carriers of the type 4 allele of the apolipoprotein E gene (apoE-epsilon4). This study has now sought, using PCR, the presence of three other herpesviruses in brain: human herpesvirus 6 (HHV6)-types A and B, herpes simplex virus type 2 (HSV2) and cytomegalovirus (CMV). HHV6 is present in a much higher proportion of the AD than of age-matched normal brains (70% vs. 40%, p = 0.003) and there is extensive overlap with the presence of HSV1 in AD brains, but HHV6, unlike HSV1, is not directly associated in AD with apoE-epsilon4. In 59%, of the AD patients' brains harbouring HHV6, type B is present while 38%. harbour both type A and type B, and 3% relatively low frequency in brains of both AD patients and normals type A. HSV2 is present at (13% and 20%), and CMV at rather higher frequencies in the two groups (36% and 35%); in neither case is the difference between the groups statistically significant. It is suggested that the striking difference in the proportion of elderly brains harbouring HSV1 and HSV2 might reflect the lower proportion of people infected with the latter, or the difference in susceptibility of the frontotemporal regions to the two viruses. In the case of HHV6, it is not possible to exclude its presence as an opportunist, but alternatively. it might enhance the damage caused by HSV1 and apoE-epsilon4 in AD, in some viral diseases it is associated with characteristic brain lesions and it also augments the damage caused by certain viruses in cell culture and in animals. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:395 / 402
页数:8
相关论文
共 42 条
[1]
Cytomegalovirus encephalitis [J].
Arribas, JR ;
Storch, GA ;
Clifford, DB ;
Tselis, AC .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (07) :577-587
[2]
ENCEPHALITIS IN IMMUNOCOMPETENT PATIENTS DUE TO HERPES-SIMPLEX VIRUS TYPE-1 OR TYPE-2 AS DETERMINED BY TYPE-SPECIFIC POLYMERASE CHAIN-REACTION AND ANTIBODY-ASSAYS OF CEREBROSPINAL-FLUID [J].
AURELIUS, E ;
JOHANSSON, B ;
SKOLDENBERG, B ;
FORSGREN, M .
JOURNAL OF MEDICAL VIROLOGY, 1993, 39 (03) :179-186
[3]
The HHV6 paradox: ubiquitous commensal or insidious pathogen? A two-step in situ PCR approach [J].
Blumberg, BM ;
Mock, DJ ;
Powers, JM ;
Ito, M ;
Assouline, JG ;
Baker, JV ;
Chen, BJ ;
Goodman, AD .
JOURNAL OF CLINICAL VIROLOGY, 2000, 16 (03) :159-178
[4]
Bremner JAG, 1999, REV MED MICROBIOL, V10, P11
[5]
NEUROINVASION AND PERSISTENCE OF HUMAN HERPESVIRUS-6 IN CHILDREN [J].
CASERTA, MT ;
HALL, CB ;
SCHNABEL, K ;
MCINTYRE, K ;
LONG, C ;
COSTANZO, M ;
DEWHURST, S ;
INSEL, R ;
EPSTEIN, LG .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (06) :1586-1589
[6]
PLAQUE-ASSOCIATED EXPRESSION OF HUMAN HERPESVIRUS-6 IN MULTIPLE-SCLEROSIS [J].
CHALLONER, PB ;
SMITH, KT ;
PARKER, JD ;
MACLEOD, DL ;
COULTER, SN ;
ROSE, TM ;
SCHULTZ, ER ;
BENNETT, JL ;
GARBER, RL ;
CHANG, M ;
SCHAD, PA ;
SEWART, PM ;
NOWINSKI, RC ;
BROWN, JP ;
BURMER, GC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7440-7444
[7]
Cytomegalovirus infections of the nervous system [J].
Cinque, P ;
Marenzi, R ;
Ceresa, D .
INTERVIROLOGY, 1997, 40 (2-3) :85-97
[8]
Dennett C, 1997, J MED VIROL, V53, P1, DOI 10.1002/(SICI)1096-9071(199709)53:1&lt
[9]
1::AID-JMV1&gt
[10]
3.0.CO