The Shraga Segal Department of Microbiology and Immunology, Faculty of Health Sciences, and The National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev,Beer-Sheva, Israel.
J Neuroimmunol. 2012 Jun 15;247(1-2):95-9. doi: 10.1016/j.jneuroim.2012.03.017. Epub 2012 Apr 10.
Aβ vaccination has been shown to induce remarkable clearance of brain amyloid plaques in mouse models of Alzheimer's disease (AD). However, the extent to which antibody-mediated Aβ clearance is affected by predominant formation of Aβ42 over Aβ40 is unclear. Here we demonstrate for the first time that in a mouse model carrying the human APP mutations KM670/671NL and the human PS1 mutation P166L, Aβ vaccination does not result in plaque clearance. This was in spite of the strong T- and B-cell immune responses evoked under the DR1501 genetic background and the activation of microglia at sites of Aβ plaques. Our findings suggest the existence of antibody-resistant forms of Aβ deposits in the brain consisting of primarily Aβ42, and shed light on the mechanisms of antibody-dependent amyloid clearance as well as novel therapeutic strategies for AD.
β 淀粉样蛋白疫苗接种已被证明可显著清除阿尔茨海默病(AD)小鼠模型中的脑淀粉样斑块。然而,抗体介导的 Aβ 清除程度受 Aβ42 相对于 Aβ40 的主要形成影响的程度尚不清楚。在这里,我们首次证明,在携带人类 APP 突变 KM670/671NL 和人类 PS1 突变 P166L 的小鼠模型中,β 淀粉样蛋白疫苗接种不会导致斑块清除。尽管在 DR1501 遗传背景下引发了强烈的 T 细胞和 B 细胞免疫反应,并且在 Aβ 斑块部位激活了小胶质细胞。我们的研究结果表明,大脑中存在主要由 Aβ42 组成的抗体抵抗形式的 Aβ 沉积物,并揭示了抗体依赖性淀粉样蛋白清除的机制以及 AD 的新治疗策略。