Solomon Beka
Department of Molecular Microbiology & Biotechnology, George S. Wise Faculty of Life Sciences, Tel-Aviv University, Ramat Aviv, Tel-Aviv 69978, Israel.
Vaccine. 2007 Apr 20;25(16):3053-6. doi: 10.1016/j.vaccine.2007.01.069. Epub 2007 Jan 22.
Beta-amyloid peptide (AbetaP) aggregation, an essentially early event in Alzheimer's disease (AD) pathogenesis, became a target for therapeutics. We developed an immunization procedure, using as antigen the EFRH peptide located at the N-terminal region of AbetaP displayed on the filamentous phage, to raise anti-beta-amyloid peptide antibodies. Data demonstrated that a bacteriophage displaying different numbers of copies of self-epitope modulates the intensity of the immuno response. This immunization procedure led to improvement in cognitive functions and alleviated amyloid pathology in a transgenic mouse (Tg) model of AD.
β-淀粉样肽(AβP)聚集是阿尔茨海默病(AD)发病机制中一个基本的早期事件,已成为治疗靶点。我们开发了一种免疫程序,使用丝状噬菌体上展示的位于AβP N端区域的EFRH肽作为抗原,以产生抗β-淀粉样肽抗体。数据表明,展示不同数量自身表位拷贝的噬菌体可调节免疫反应的强度。这种免疫程序改善了AD转基因小鼠(Tg)模型的认知功能并减轻了淀粉样病理变化。