IMR Press / FBL / Volume 14 / Issue 10 / DOI: 10.2741/3496

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article
Identification of autoantibody against beta-amyloid peptide in the serum of elderly
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1 Department of Biochemistry and Cancer Research Institute, Seoul National University College of Medicine, Seoul, 110-799, Korea
2 Department of Neurology, Samsung Medical Center, Seoul, 135-710, Korea
3 Department of Neurology, Seoul National University College of Medicine, Seoul, 110-799, Korea
4 Digital Biotech, Inc., Gyeongi, 425-838, Korea
Front. Biosci. (Landmark Ed) 2009, 14(10), 3879–3883; https://doi.org/10.2741/3496
Published: 1 January 2009
Abstract

Alzheimer's disease (AD) is characterized by two major neurological features: amyloid deposits and neurofibrillary tangles in the brain. According to the amyloid cascade hypothesis, accumulation of amyloid-beta peptide (A-beta) plays a central role in the pathogenesis of AD. Several lines of evidence suggest that antibodies against A-beta play a protective role in the neuropathology of AD. In this study, we describe the purification of an autoantibody against A-beta from human serum using affinity purification method. The purified autoantibody recognized A-beta deposits in the brain of aged Tg2676 mice, an animal model of AD. The serum levels of anti-A-beta autoantibody correlated inversely with age in both AD patients and control non-demented elderly subjects. Furthermore, the levels were significantly lower in AD patients compared with the age-matched control subjects. It is the first time to show the identification of endogenous anti-A-beta autoantibody in human serum and suggesting that serum levels of anti-A-beta autoantibody might be a good biomarker for AD patients.

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