Aβ42 vaccine on the Tg2576 Alzheimer model mice

Mikio Shoji, Yasuo Harigaya, Etsuro Matsubara, Takeshi Kawarabayashi, Tetsuro Murakami, Nobuhiko Oomori, Keiko Sato, Isao Nagano, Koji Abe

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

In 1999, Schenk et al. [Nature 400 (1999) 173] reported remarkable improvement of Aβ amyloid burden in the transgenic mice brain by immunization with Aβ42 peptides. Soon after, four independent institutes showed the same findings on senile plaque amyloid and improvement of memory disturbance confirming the effect of Aβ vaccine on brain Aβ amyloidosis. In July 2001, Elan Corporation started cooperative Phase I study of AN-1792, synthetic Aβ42 peptide. In September, Phase II study of 375 Alzheimer patients began in Europe. Because of 15 cases of encephalitis in March 2002, this drug trial was suspended. This is serious accident for patients, family and specialists, who hope for a curative therapy for Alzheimer's disease (AD). However, this result provided new insight that brain amyloidosis is reversible. Prompt evaluation of candidate drugs such as anti-Aβ antibody, β-secretase inhibitor or anti-Aβ aggregation should be necessary in the near future.

Original languageEnglish
Pages (from-to)399-403
Number of pages5
JournalInternational Congress Series
Volume1252
Issue numberC
DOIs
Publication statusPublished - Jun 1 2003

Keywords

  • Alzheimer's disease
  • Aβ amyloid
  • Aβ vaccine
  • Efficacy
  • Treatment

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'Aβ42 vaccine on the Tg2576 Alzheimer model mice'. Together they form a unique fingerprint.

  • Cite this

    Shoji, M., Harigaya, Y., Matsubara, E., Kawarabayashi, T., Murakami, T., Oomori, N., Sato, K., Nagano, I., & Abe, K. (2003). Aβ42 vaccine on the Tg2576 Alzheimer model mice. International Congress Series, 1252(C), 399-403. https://doi.org/10.1016/S0531-5131(03)00101-8