Epitopes described in "Transcutaneous beta-amyloid immunization reduces cerebral beta-amyloid deposits without T cell infiltration and microhemorrhage."

Reference
Article Authors:William V Nikolic; Yun Bai; Demian Obregon; Huayan Hou; Takashi Mori; Jin Zeng; Jared Ehrhart; R Douglas Shytle; Brian Giunta; Dave Morgan; Terrence Town; Jun Tan
Article Title:Transcutaneous beta-amyloid immunization reduces cerebral beta-amyloid deposits without T cell infiltration and microhemorrhage.
Reference Detail
Reference ID:1003692
Abstract:Alzheimer's disease (AD) immunotherapy accomplished by vaccination with beta-amyloid (Abeta) peptide has proved efficacious in AD mouse models. However, "active" Abeta vaccination strategies for the treatment of cerebral amyloidosis without concurrent induction of detrimental side effects are lacking. We have developed a transcutaneous (t.c.) Abeta vaccination approach and evaluated efficacy and monitored for deleterious side effects, including meningoencephalitis and microhemorrhage, in WT mice and a transgenic mouse model of AD. We demonstrate that t.c. immunization of WT mice with aggregated Abeta(1-42) plus the adjuvant cholera toxin (CT) results in high-titer Abeta antibodies (mainly of the Ig G1 class) and Abeta(1-42)-specific splenocyte immune responses. Confocal microscopy of the t.c. immunization site revealed Langerhans cells in areas of the skin containing the Abeta(1-42) immunogen, suggesting that these unique innate immune cells participate in Abeta(1-42) antigen processing. To evaluate the efficacy of t.c. immunization in reducing cerebral amyloidosis, transgenic PSAPP (APPsw, PSEN1dE9) mice were immunized with aggregated Abeta(1-42) peptide plus CT. Similar to WT mice, PSAPP mice showed high Abeta antibody titers. Most importantly, t.c. immunization with Abeta(1-42) plus CT resulted in significant decreases in cerebral Abeta(1-40,42) levels coincident with increased circulating levels of Abeta(1-40,42), suggesting brain-to-blood efflux of Abeta. Reduction in cerebral amyloidosis was not associated with deleterious side effects, including brain T cell infiltration or cerebral microhemorrhage. Together, these data suggest that t.c. immunization constitutes an effective and potentially safe treatment strategy for AD.
Date:2007
Reference Type:Literature
PubMed ID:17264212
Journal:Proc Natl Acad Sci U S A
Journal Volume:104
Article Pages:2507-12
Journal ISSN:1091-6490
Article Chemical List:Amyloid beta-Peptides;Antibodies;Peptide Fragments;amyloid beta-protein (1-42)
Article MeSH List:Alzheimer Disease(pathology; therapy); Amyloid beta-Peptides(analysis; immunology; therapeutic use); Amyloidosis; Animals; Antibodies(blood); Antibody Formation(drug effects); Brain(pathology); Cerebral Hemorrhage(etiology); Chemotaxis, Leukocyte; Langerhans Cells(immunology); Meningoencephalitis(etiology); Mice; Peptide Fragments(immunology; therapeutic use); T-Lymphocytes; Treatment Outcome; Vaccination(adverse effects; methods)
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