Skip to main navigation Skip to search Skip to main content

The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers

  • Matteo Stravalaci
  • , Laura Tapella
  • , Marten Beeg
  • , Alessandro Rossi
  • , Pooja Joshi
  • , Erika Pizzi
  • , Michele Mazzanti
  • , Claudia Balducci
  • , Gianluigi Forloni
  • , Emiliano Biasini
  • , Mario Salmona
  • , Luisa DIomede
  • , Roberto Chiesa
  • , Marco Gobbi

Research output: Contribution to journalArticlepeer-review

Abstract

15B3 is a monoclonal IgM antibody that selectively detects pathological aggregates of the prion protein (PrP). We report the unexpected finding that 15B3 also recognizes oligomeric but not monomeric forms of amyloid-β (Aβ)42, an aggregating peptide implicated in the pathogenesis of Alzheimer's disease (AD). The 15B3 antibody: i) inhibits the binding of synthetic Aβ42 oligomers to recombinant PrP and neuronal membranes; ii) prevents oligomer-induced membrane depolarization; iii) antagonizes the inhibitory effects of oligomers on the physiological pharyngeal contractions of the nematode Caenorhabditis elegans; and iv) counteracts the memory deficits induced by intracerebroventricular injection of Aβ42 oligomers in mice. Thus this antibody binds to pathologically relevant forms of Aβ, and offers a potential research, diagnostic, and therapeutic tool for AD.

Original languageEnglish
Pages (from-to)1485-1497
Number of pages13
JournalJournal of Alzheimer's Disease
Volume53
Issue number4
DOIs
Publication statusPublished - 2016
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • 15B3 antibody
  • Alzheimer's disease
  • Amyloid beta-protein (1-42)
  • Oligomers
  • Oligomers
  • Prion protein
  • Prions

Fingerprint

Dive into the research topics of 'The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers'. Together they form a unique fingerprint.

Cite this