Reduced levels of amyloid β-peptide antibody in Alzheimer disease

被引:220
作者
Du, Y
Dodel, R
Hampel, H
Buerger, K
Lin, S
Eastwood, B
Bales, K
Gao, F
Moeller, HJ
Oertel, W
Farlow, M
Paul, S
机构
[1] Indiana Univ Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46285 USA
[2] Indiana Univ Sch Med, Dept Neurol, Indianapolis, IN 46285 USA
[3] Indiana Univ Sch Med, Dept Psychiat, Indianapolis, IN 46285 USA
[4] Univ Marburg, Dept Neurol, Marburg, Germany
[5] Univ Munich, Dementia Res Sect, Munich, Germany
[6] Univ Munich, Memory Clin, Munich, Germany
[7] Eli Lilly & Co, Lilly Res Labs, Dept Stat & Math Sci, Neurosci Discovery Res, Indianapolis, IN 46285 USA
关键词
D O I
10.1212/WNL.57.5.801
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To investigate whether it was possible to detect the presence and different levels of naturally occurring anti-beta -amyloid (A beta) antibodies in the CSF of patients with AD and age-matched controls by employing a sensitive ELISA. Background: Immunization with preaggregated amyloid beta -peptide (A beta (1-42)) and administration of antibodies against A beta into amyloid precursor protein APP(V717F)-transgenic mice (an animal model of AD) have recently been reported to dramatically reduce amyloid plaque deposition, neuritic dystrophy, and astrogliosis, most likely by enhancing A beta clearance from brain. Methods: A sensitive ELISA was performed to detect levels of naturally occurring anti-A beta antibodies in the CSF of patients with AD and age-matched controls. Additionally, an immunoprecipitation assay was performed to confirm that naturally occurring anti-A beta antibodies also exist in the human blood. Result: Naturally occurring antibodies directed against A beta were found in the CSF and plasma of patients with AD and healthy control subjects. Moreover, CSF anti-A beta antibody titers are significantly lower in patients with AD compared with healthy control subjects. Conclusion: Naturally occurring antibodies directed against A beta exist in human CSF and plasma. The CSF anti-A beta antibody titers may be helpful in better understanding the effects of future immunologic therapies for AD.
引用
收藏
页码:801 / 805
页数:5
相关论文
共 18 条
  • [1] ARMITAGE P, 1994, STAT METHODS MED RES, P389
  • [2] Peripherally administered antibodies against amyloid β-peptide enter the central nervous system and reduce pathology in a mouse model of Alzheimer disease
    Bard, F
    Cannon, C
    Barbour, R
    Burke, RL
    Games, D
    Grajeda, H
    Guido, T
    Hu, K
    Huang, JP
    Johnson-Wood, K
    Khan, K
    Kholodenko, D
    Lee, M
    Lieberburg, I
    Motter, R
    Nguyen, M
    Soriano, F
    Vasquez, N
    Weiss, K
    Welch, B
    Seubert, P
    Schenk, D
    Yednock, T
    [J]. NATURE MEDICINE, 2000, 6 (08) : 916 - 919
  • [3] Alzheimer's disease - The ins and outs of amyloid-beta
    Beyreuther, K
    Masters, CL
    [J]. NATURE, 1997, 389 (6652) : 677 - 678
  • [4] A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain
    De Strooper, B
    Annaert, W
    Cupers, P
    Saftig, P
    Craessaerts, K
    Mumm, JS
    Schroeter, EH
    Schrijvers, V
    Wolfe, MS
    Ray, WJ
    Goate, A
    Kopan, R
    [J]. NATURE, 1999, 398 (6727) : 518 - 522
  • [5] ALZHEIMER-TYPE NEUROPATHOLOGY IN TRANSGENIC MICE OVEREXPRESSING V717F BETA-AMYLOID PRECURSOR PROTEIN
    GAMES, D
    ADAMS, D
    ALESSANDRINI, R
    BARBOUR, R
    BERTHELETTE, P
    BLACKWELL, C
    CARR, T
    CLEMENS, J
    DONALDSON, T
    GILLESPIE, F
    GUIDO, T
    HAGOPIAN, S
    JOHNSONWOOD, K
    KHAN, K
    LEE, M
    LEIBOWITZ, P
    LIEBERBURG, I
    LITTLE, S
    MASLIAH, E
    MCCONLOGUE, L
    MONTOYAZAVALA, M
    MUCKE, L
    PAGANINI, L
    PENNIMAN, E
    POWER, M
    SCHENK, D
    SEUBERT, P
    SNYDER, B
    SORIANO, F
    TAN, H
    VITALE, J
    WADSWORTH, S
    WOLOZIN, B
    ZHAO, J
    [J]. NATURE, 1995, 373 (6514) : 523 - 527
  • [6] ALZHEIMERS-DISEASE - INITIAL REPORT OF THE PURIFICATION AND CHARACTERIZATION OF A NOVEL CEREBROVASCULAR AMYLOID PROTEIN
    GLENNER, GG
    WONG, CW
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (03) : 885 - 890
  • [7] AMYLOID BETA-PEPTIDE IS PRODUCED BY CULTURED-CELLS DURING NORMAL METABOLISM
    HAASS, C
    SCHLOSSMACHER, MG
    HUNG, AY
    VIGOPELFREY, C
    MELLON, A
    OSTASZEWSKI, BL
    LIEBERBURG, I
    KOO, EH
    SCHENK, D
    TEPLOW, DB
    SELKOE, DJ
    [J]. NATURE, 1992, 359 (6393) : 322 - 325
  • [8] THE PRECURSOR OF ALZHEIMERS-DISEASE AMYLOID-A4 PROTEIN RESEMBLES A CELL-SURFACE RECEPTOR
    KANG, J
    LEMAIRE, HG
    UNTERBECK, A
    SALBAUM, JM
    MASTERS, CL
    GRZESCHIK, KH
    MULTHAUP, G
    BEYREUTHER, K
    MULLERHILL, B
    [J]. NATURE, 1987, 325 (6106) : 733 - 736
  • [9] BETA-AMYLOID NEUROTOXICITY REQUIRES FIBRIL FORMATION AND IS INHIBITED BY CONGO RED
    LORENZO, A
    YANKNER, BA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) : 12243 - 12247
  • [10] NEURONAL ORIGIN OF A CEREBRAL AMYLOID - NEUROFIBRILLARY TANGLES OF ALZHEIMERS-DISEASE CONTAIN THE SAME PROTEIN AS THE AMYLOID OF PLAQUE CORES AND BLOOD-VESSELS
    MASTERS, CL
    MULTHAUP, G
    SIMMS, G
    POTTGIESSER, J
    MARTINS, RN
    BEYREUTHER, K
    [J]. EMBO JOURNAL, 1985, 4 (11) : 2757 - 2763