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T 细胞衰老与阿尔茨海默病。

T cell aging and Alzheimer's disease.

机构信息

Key Laboratory of Major Chronic Diseases of Nervous System of Liaoning Province, Health Sciences Institute of China Medical University, Shenyang, China.

Department of Rehabilitation, Shengjing Hospital of China Medical University, Shenyang, China.

出版信息

Front Immunol. 2023 Apr 4;14:1154699. doi: 10.3389/fimmu.2023.1154699. eCollection 2023.


DOI:10.3389/fimmu.2023.1154699
PMID:37081887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10110977/
Abstract

The brain has long been considered an immune-privileged organ due to the presence of the blood-brain barrier (BBB). However, recent discoveries have revealed the underestimated role of T cells in the brain through the meningeal lymphatic system. Age is the primary risk factor for Alzheimer's disease (AD), resulting in marked age-dependent changes in T cells. Manipulating peripheral T cell immune response has been shown to impact AD, but the relationship between T cell aging and AD remains poorly understood. Given the limited success of targeting amyloid beta (Aβ) and the growing evidence of T cells' involvement in non-lymphoid organ aging, a deeper understanding of the relationship between T cells and AD in the context of aging is crucial for advancing therapeutic progress. In this review, we comprehensively examine existing studies on T cells and AD and offer an integrated perspective on their interconnections in the context of aging. This understanding can inform the development of new interventions to prevent or treat AD.

摘要

大脑长期以来被认为是免疫特权器官,这要归功于血脑屏障(BBB)的存在。然而,最近的发现揭示了脑膜淋巴管系统中 T 细胞在大脑中的被低估的作用。年龄是阿尔茨海默病(AD)的主要风险因素,导致 T 细胞出现明显的年龄依赖性变化。已经证明操纵外周 T 细胞免疫反应会影响 AD,但 T 细胞衰老与 AD 之间的关系仍知之甚少。鉴于靶向淀粉样蛋白β(Aβ)的有限成功,以及越来越多的证据表明 T 细胞参与非淋巴器官衰老,深入了解衰老背景下 T 细胞与 AD 之间的关系对于推进治疗进展至关重要。在这篇综述中,我们全面检查了现有的关于 T 细胞和 AD 的研究,并提供了它们在衰老背景下相互关系的综合观点。这种理解可以为预防或治疗 AD 提供新的干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8265/10110977/f36be6ab5c01/fimmu-14-1154699-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8265/10110977/2e5550c61b94/fimmu-14-1154699-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8265/10110977/f36be6ab5c01/fimmu-14-1154699-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8265/10110977/2e5550c61b94/fimmu-14-1154699-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8265/10110977/f36be6ab5c01/fimmu-14-1154699-g002.jpg

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[10]
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本文引用的文献

[1]
Accumulation of cytotoxic T cells in the aged CNS leads to axon degeneration and contributes to cognitive and motor decline.

Nat Aging. 2021-4

[2]
TRIB2 safeguards naive T cell homeostasis during aging.

Cell Rep. 2023-3-28

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Nat Immunol. 2023-1

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Front Aging. 2022-11-7

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J Neuroinflammation. 2021-11-19

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