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主动 Aβ 疫苗接种未能增强 Aβ42 驱动病理的阿尔茨海默病小鼠模型中的淀粉样蛋白清除。

Active Aβ vaccination fails to enhance amyloid clearance in a mouse model of Alzheimer's disease with Aβ42-driven pathology.

机构信息

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.

出版信息

J Neuroimmunol. 2012 Jun 15;247(1-2):95-9. doi: 10.1016/j.jneuroim.2012.03.017. Epub 2012 Apr 10.

Abstract

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.

摘要

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。

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