Guillot-Sestier Marie-Victoire, Doty Kevin R, Town Terrence
Zilkha Neurogenetic Institute, Keck School of Medicine of the University of Southern California, 1501 San Pablo Street, Room 337, Los Angeles, CA 90089-2821, USA.
Zilkha Neurogenetic Institute, Keck School of Medicine of the University of Southern California, 1501 San Pablo Street, Room 337, Los Angeles, CA 90089-2821, USA.
Trends Neurosci. 2015 Nov;38(11):674-681. doi: 10.1016/j.tins.2015.08.008.
Alzheimer's disease (AD) is the most common age-related dementia. Pathognomonic accumulation of cerebral β-amyloid plaques likely results from imbalanced production and removal of amyloid-β (Aβ) peptides. In AD, innate immune cells lose their ability to restrict cerebral Aβ accumulation. At least in principle, mononuclear phagocytes can be enlisted to clear Aβ/β-amyloid from the brain. While the classical focus has been on dampening neuroinflammation in the context of AD, we hypothesize that rebalancing cerebral innate immunity by inhibiting actions of key anti-inflammatory cytokines returns the brain to a physiological state. Recent experiments demonstrating beneficial effects of blocking anti-inflammatory cytokine signaling in preclinical mouse models provide supportive evidence. This concept represents an important step toward innate immune-targeted therapy to combat AD.
阿尔茨海默病(AD)是最常见的与年龄相关的痴呆症。大脑β-淀粉样蛋白斑块的特征性积累可能是由于淀粉样蛋白-β(Aβ)肽的产生和清除失衡所致。在AD中,先天免疫细胞失去了限制大脑Aβ积累的能力。至少在理论上,可以利用单核吞噬细胞清除大脑中的Aβ/β-淀粉样蛋白。虽然传统上一直关注在AD背景下减轻神经炎症,但我们假设通过抑制关键抗炎细胞因子的作用来重新平衡大脑先天免疫,可使大脑恢复到生理状态。最近在临床前小鼠模型中证明阻断抗炎细胞因子信号传导具有有益效果的实验提供了支持性证据。这一概念代表了对抗AD的先天免疫靶向治疗的重要一步。