Generation of anti-β-amyloid antibodies via phage display technology towards Alzheimer's disease vaccination

被引:14
作者
Solomon, B [1 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Mol Microbiol & Biotechnol, IL-69978 Tel Aviv, Israel
关键词
phage display; anti-aggregating epitope; Alzheimer's disease; IMMUNIZATION; PLAQUES; PEPTIDE; EPITOPE;
D O I
10.1016/j.vaccine.2005.01.034
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The pathology of Alzheimer's disease (AD) shows a significant correlation between beta-amyloid peptide (beta AP) deposition and the clinical severity of dementia. The ability of site-directed antibodies towards the N-terminal region of beta-amyloid peptide to suppress in vitro formation of toxic beta-amyloid serves as a factual basis for in vivo investigations. We localized the epitope of these anti-aggregating antibodies, and injection of phage displaying this epitope induced antibodies against the whole anti-beta-amyloid peptide. In Alzheimer's diseased transgenic mice, these antibodies are delivered from the periphery to the CNS preventing beta-amyloid formation and/or dissolving such aggregates. Performance of such antigens opens up possibilities for development of an efficient, long-lasting immunization procedure for treatment of Alzheimer's disease. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2327 / 2330
页数:4
相关论文
共 10 条
  • [1] N-terminal EFRH sequence of Alzheimer's β-amyloid peptide represents the epitope of its anti-aggregating antibodies
    Frenkel, D
    Balass, M
    Solomon, B
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1998, 88 (1-2) : 85 - 90
  • [2] Immunization against Alzheimer's β-amyloid plaques via EFRH phage administration
    Frenkel, D
    Katz, O
    Solomon, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (21) : 11455 - 11459
  • [3] Galfre G, 1996, METHOD ENZYMOL, V267, P109
  • [4] EFRH-phage immunization of Alzheimer's disease animal model improves behavioral performance in Morris water maze trials
    Lavie, V
    Becker, M
    Cohen-Kupiec, R
    Yacoby, I
    Koppel, R
    Wedenig, M
    Hutter-Paier, B
    Solomon, B
    [J]. JOURNAL OF MOLECULAR NEUROSCIENCE, 2004, 24 (01) : 105 - 113
  • [5] REVERSIBLE INVITRO GROWTH OF ALZHEIMER-DISEASE BETA-AMYLOID PLAQUES BY DEPOSITION OF LABELED AMYLOID PEPTIDE
    MAGGIO, JE
    STIMSON, ER
    GHILARDI, JR
    ALLEN, CJ
    DAHL, CE
    WHITCOMB, DC
    VIGNA, SR
    VINTERS, HV
    LABENSKI, ME
    MANTYH, PW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) : 5462 - 5466
  • [6] MOLECULAR-MODELS AND STRUCTURAL COMPARISONS OF NATIVE AND MUTANT CLASS-I FILAMENTOUS BACTERIOPHAGES FF (FD, F1, M13), IF1 AND IKE
    MARVIN, DA
    HALE, RD
    NAVE, C
    CITTERICH, MH
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1994, 235 (01) : 260 - 286
  • [7] Immunization with amyloid-β attenuates Alzheimer disease-like pathology in the PDAPP mouse
    Schenk, D
    Barbour, R
    Dunn, W
    Gordon, G
    Grajeda, H
    Guido, T
    Hu, K
    Huang, JP
    Johnson-Wood, K
    Khan, K
    Kholodenko, D
    Lee, M
    Liao, ZM
    Lieberburg, I
    Motter, R
    Mutter, L
    Soriano, F
    Shopp, G
    Vasquez, N
    Vandevert, C
    Walker, S
    Wogulis, M
    Yednock, T
    Games, D
    Seubert, P
    [J]. NATURE, 1999, 400 (6740) : 173 - 177
  • [8] Disaggregation of Alzheimer beta-amyloid by site-directed mAb
    Solomon, B
    Koppel, R
    Frankel, D
    HananAharon, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) : 4109 - 4112
  • [9] Zuercher AW, 2000, EUR J IMMUNOL, V30, P128, DOI 10.1002/1521-4141(200001)30:1<128::AID-IMMU128>3.0.CO
  • [10] 2-X