TY - JOUR
T1 - Generation of anti-β-amyloid antibodies via phage display technology towards Alzheimer's disease vaccination
AU - Solomon, Beka
N1 - Funding Information:
The author wishes to thank the Institute for the Study of Aging, USA, for funding. The author appreciates the work of and expresses thanks to Dr. V. Lavie and Dr. M. Beker for neuropathology studies, to Dr. R. Cohen-Kupiec for preparation of the antigen, and to F. Margolin for editing the manuscript.
PY - 2005/3/18
Y1 - 2005/3/18
N2 - The pathology of Alzheimer's disease (AD) shows a significant correlation between β-amyloid peptide (βAP) deposition and the clinical severity of dementia. The ability of site-directed antibodies towards the N-terminal region of β-amyloid peptide to suppress in vitro formation of toxic β-amyloid serves as a factual basis for in vivo investigations. We localized the epitope of these anti-aggregating antibodies, and injection of phage displaying this epitope induced antibodies against the whole anti-β-amyloid peptide. In Alzheimer's diseased transgenic mice, these antibodies are delivered from the periphery to the CNS preventing β-amyloid formation and/or dissolving such aggregates. Performance of such antigens opens up possibilities for development of an efficient, long-lasting immunization procedure for treatment of Alzheimer's disease.
AB - The pathology of Alzheimer's disease (AD) shows a significant correlation between β-amyloid peptide (βAP) deposition and the clinical severity of dementia. The ability of site-directed antibodies towards the N-terminal region of β-amyloid peptide to suppress in vitro formation of toxic β-amyloid serves as a factual basis for in vivo investigations. We localized the epitope of these anti-aggregating antibodies, and injection of phage displaying this epitope induced antibodies against the whole anti-β-amyloid peptide. In Alzheimer's diseased transgenic mice, these antibodies are delivered from the periphery to the CNS preventing β-amyloid formation and/or dissolving such aggregates. Performance of such antigens opens up possibilities for development of an efficient, long-lasting immunization procedure for treatment of Alzheimer's disease.
KW - Alzheimer's disease
KW - Anti-aggregating epitope
KW - Phage display
UR - http://www.scopus.com/inward/record.url?scp=14844327972&partnerID=8YFLogxK
U2 - 10.1016/j.vaccine.2005.01.034
DO - 10.1016/j.vaccine.2005.01.034
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AN - SCOPUS:14844327972
SN - 0264-410X
VL - 23
SP - 2327
EP - 2330
JO - Vaccine
JF - Vaccine
IS - 17-18
ER -