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pubmed-article:1438191pubmed:abstractTextAlzheimer disease (AD) is characterized by excessive deposition of the beta-amyloid peptide (beta-AP) in the central nervous system. Although several lines of evidence suggest that beta-AP is neurotoxic, a mechanism for beta-AP toxicity in AD brain remains unclear. In this paper we provide both direct in vitro evidence that beta-AP can bind and activate the classical complement cytolytic pathway in the absence of antibody and indirect in situ evidence that such actions occur in the AD brain in association with areas of AD pathology.lld:pubmed
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pubmed-article:1438191pubmed:articleTitleComplement activation by beta-amyloid in Alzheimer disease.lld:pubmed
pubmed-article:1438191pubmed:affiliationL. J. Roberts Center, Sun Health Research Institute, Sun City, AZ 85351.lld:pubmed
pubmed-article:1438191pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1438191pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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