4.7 Article

Anti-Aβ single-chain antibody delivery via adeno-associated virus for treatment of Alzheimer's disease

期刊

NEUROBIOLOGY OF DISEASE
卷 23, 期 3, 页码 502-511

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2006.04.012

关键词

gene therapy; vaccine; amyloid protein; amyloid plaque; transgenic mouse; immune therapy

资金

  1. NINDS NIH HHS [R01 NS043947, R01 NS043947-04, NS43947] Funding Source: Medline

向作者/读者索取更多资源

Immunization of mouse models of Alzheimer disease (AD) with amyloid-peptide (A) reduces A beta deposits and attenuates their memory and learning deficits. Recent clinical trials were halted due to meningoencephalitis, presumably induced by T cell mediated and/or Fc-mediated immune responses. Because injection of anti-A beta F(ab')2 antibodies also induces clearance of amyloid plaques in AD mouse models, we have tested a novel gene therapy modality where an adeno-associated virus (AAV) encoding anti-alpha single-chain antibody (scFv) is injected into the corticohippocampal regions of AD mouse models. One year after injection, expression of scFv was readily detectable in the neurons of the hippocampus without discernible neurotoxicity. AD mouse models subjected to AAV injection had much less amyloid deposits at the injection sites than the mouse models subjected to PBS injection. Because the scFv lacks the Fc portion of the immunoglobulin molecule, this modality may be a feasible solution for AD without eliciting inflammation. (c) 2006 Elsevier Inc. All rights reserved.

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