| Literature DB >> 18486927 |
Hiroaki Taguchi1, Stephanie Planque, Yasuhiro Nishiyama, Paul Szabo, Marc E Weksler, Robert P Friedland, Sudhir Paul.
Abstract
Immunoglobulins (Igs) that bind amyloid beta peptide (Abeta) are under clinical trials for immunotherapy of Alzheimer disease (AD). We have identified IgMs and recombinant Ig fragments that hydrolyze Abeta. Hydrolysis of peripheral Abeta by the IgMs may induce increased Abeta release from the brain. The catalytic IgMs are increased in AD patients, presumably reflecting a protective autoimmune response. Reduced Abeta aggregation and neurotoxicity attributable to the catalytic function were evident. These findings provide a foundation for development of catalytic Igs for AD immunotherapy.Entities:
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Year: 2008 PMID: 18486927 PMCID: PMC2430036 DOI: 10.1016/j.autrev.2008.03.004
Source DB: PubMed Journal: Autoimmun Rev ISSN: 1568-9972 Impact factor: 9.754