Solomon Beka
Department of Molecular Microbiology and Biotechnology, George S. Wise Faculty of Life Sciences, Tel-Aviv University, Ramat Aviv, Tel-Aviv 69978, Israel.
Vaccine. 2005 Mar 18;23(17-18):2327-30. doi: 10.1016/j.vaccine.2005.01.034.
The pathology of Alzheimer's disease (AD) shows a significant correlation between beta-amyloid peptide (betaAP) deposition and the clinical severity of dementia. The ability of site-directed antibodies towards the N-terminal region of beta-amyloid peptide to suppress in vitro formation of toxic beta-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-beta-amyloid peptide. In Alzheimer's diseased transgenic mice, these antibodies are delivered from the periphery to the CNS preventing beta-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.
阿尔茨海默病(AD)的病理学研究表明,β-淀粉样肽(βAP)沉积与痴呆的临床严重程度之间存在显著相关性。针对β-淀粉样肽N端区域的定点抗体在体外抑制有毒β-淀粉样蛋白形成的能力,为体内研究提供了事实依据。我们定位了这些抗聚集抗体的表位,注射展示该表位的噬菌体可诱导产生针对整个抗β-淀粉样肽的抗体。在患阿尔茨海默病的转基因小鼠中,这些抗体从外周递送至中枢神经系统,可防止β-淀粉样蛋白的形成和/或溶解此类聚集体。此类抗原的应用为开发高效、持久的阿尔茨海默病免疫治疗方法开辟了可能性。