Vaccination with (1-11)E2 in alum efficiently induces an antibody response to β-amyloid without affecting brain β-amyloid load and microglia activation in 3xTg mice

Aging Clin Exp Res. 2021 May;33(5):1383-1387. doi: 10.1007/s40520-019-01414-0. Epub 2019 Nov 22.

Abstract

Immunization against β-amyloid (Aβ) is pursued as a possible strategy for the prevention of Alzheimer's disease (AD). In clinical trials, Aβ 1-42 proved poorly immunogenic and caused severe adverse effects; therefore, safer and more immunogenic candidate vaccines are needed. Multimeric protein (1-11)E2 is able to induce an antibody response to Aβ, immunological memory, and IL-4 production, with no concomitant anti-Aβ T cell response. Antisera recognize Aβ oligomers, protofibrils, and fibrils. In this study, we evaluated the effect of prophylactic immunization with three doses of (1-11)E2 in alum in the 3xTg mouse model of AD. Immunization with (1-11)E2 efficiently induced anti-Aβ antibodies, but afforded no protection against Aβ accumulation and neuroinflammation. The identification of the features of the anti-Aβ immune response that correlate with the ability to prevent Aβ accumulation remains an open problem that deserves further investigation.

Keywords: Alzheimer’s disease; Antibody response; Immunization; β-amyloid.

MeSH terms

  • Alum Compounds
  • Alzheimer Disease*
  • Amyloid beta-Peptides* / metabolism
  • Animals
  • Antibody Formation
  • Brain / metabolism
  • Disease Models, Animal
  • Mice
  • Mice, Inbred C57BL
  • Microglia / metabolism
  • Peptide Fragments
  • Vaccination

Substances

  • Alum Compounds
  • Amyloid beta-Peptides
  • Peptide Fragments
  • aluminum sulfate