| Literature DB >> 12379846 |
Christoph Hock1, Uwe Konietzko, Andreas Papassotiropoulos, Axel Wollmer, Johannes Streffer, Ruth C von Rotz, Gabriela Davey, Eva Moritz, Roger M Nitsch.
Abstract
To characterize antibodies produced in humans in response to Abeta42 vaccination, we carried out immunohistochemical examinations of the brains of both transgenic mice and human patients with beta-amyloid pathology. We collected sera from patients with Alzheimer disease who received a primary injection of pre-aggregated Abeta42 followed by one booster injection in a placebo-controlled study. Antibodies in immune sera recognized beta-amyloid plaques, diffuse Abeta deposits and vascular beta-amyloid in brain blood vessels. The antibodies did not cross-react with native full-length beta-amyloid precursor protein or its physiological derivatives, including soluble Abeta42. These findings indicate that vaccination of AD patients with Abeta42 induces antibodies that have a high degree of selectivity for the pathogenic target structures. Whether vaccination to produce antibodies against beta-amyloid will halt the cognitive decline in AD will depend upon clinical assessments over time.Entities:
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Year: 2002 PMID: 12379846 DOI: 10.1038/nm783
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440