New insights into innate immunity in Alzheimer's disease: from APOE protective variants to therapies

被引:3
|
作者
Chen, Yun [1 ]
Holtzman, David M. [1 ]
机构
[1] Washington Univ St Louis, Hope Ctr Neurol Disorders, Knight Alzheimers Dis Res Ctr, Dept Neurol, St. Louis, MO 63110 USA
关键词
HUMAN APOLIPOPROTEIN-E; TAU-MEDIATED NEURODEGENERATION; MOUSE MODEL; AMYLOID DEPOSITION; GENE-THERAPY; BETA PLAQUES; ANTIBODY; MICROGLIA; ACCUMULATION; BINDING;
D O I
10.1016/j.it.2024.08.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent discoveries of rare variants of human APOE may shed light on novel therapeutic strategies for Alzheimer's disease (AD). Here, we highlight the newly identified protective variant [APOE3 Christchurch (APOE3ch, R136S)] as an example. We summarize human AD and mouse amyloidosis and tauopathy studies from the past 5 years that have been associated with this R136S variant. We also propose a potential mechanism for how this point mutation might lead to protection against AD pathology, from the molecular level, to cells, to mouse models, and potentially, to humans. Lastly, we extend our discussion of the recent insights gained regarding different APOE variants to putative therapeutic approaches in AD.
引用
收藏
页码:768 / 782
页数:15
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