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解读阿尔茨海默病中的神经炎症:多组学与人工智能驱动的精准医学视角

Decoding neuroinflammation in Alzheimer's disease: a multi-omics and AI-driven perspective for precision medicine.

作者信息

Lin Shiyu, Zhan Yijun, Wang Ruiqi, Pei Jian

机构信息

Department of Acupuncture, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Front Immunol. 2025 Jun 18;16:1616899. doi: 10.3389/fimmu.2025.1616899. eCollection 2025.


DOI:10.3389/fimmu.2025.1616899
PMID:40607399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12213348/
Abstract

Alzheimer's disease (AD) is a common neurodegenerative disease, which is characterized by β-amyloid (Aβ) deposition, Tau hyperphosphorylation, synaptic dysfunction and chronic neuroinflammation. Despite significant advances in research in recent years, effective therapeutic options remain limited. The development of single-cell RNA sequencing (scRNA-seq) has made it possible to analyze cellular heterogeneity in AD brain tissues at high resolution, breaking through the limitation of signal averaging in traditional large-scale tissue analysis. This technology has led to the discovery of novel disease-associated cell subsets, such as pro-inflammatory microglia and reactive astrocytes, and the identification of key molecular markers linked to disease progression. Integrating scRNA-seq with AI-driven analytics and multi-omics platforms further enhances our ability to decode the intricate immune-inflammatory networks underlying AD. This strategy is expected to achieve accurate classification and early diagnosis of AD subtypes, and promote the development of individualized treatment strategies based on individual molecular and immune characteristics.

摘要

阿尔茨海默病(AD)是一种常见的神经退行性疾病,其特征为β-淀粉样蛋白(Aβ)沉积、 Tau蛋白过度磷酸化、突触功能障碍和慢性神经炎症。尽管近年来研究取得了重大进展,但有效的治疗选择仍然有限。单细胞RNA测序(scRNA-seq)技术的发展使得在高分辨率下分析AD脑组织中的细胞异质性成为可能,突破了传统大规模组织分析中信号平均化的限制。这项技术促使人们发现了新的疾病相关细胞亚群,如促炎性小胶质细胞和反应性星形胶质细胞,并确定了与疾病进展相关的关键分子标记。将scRNA-seq与人工智能驱动的分析方法和多组学平台相结合,进一步增强了我们解码AD复杂免疫炎症网络的能力。这一策略有望实现AD亚型的准确分类和早期诊断,并推动基于个体分子和免疫特征的个体化治疗策略的发展。

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[1]
Decoding neuroinflammation in Alzheimer's disease: a multi-omics and AI-driven perspective for precision medicine.

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本文引用的文献

[1]
Single-cell atlas of endothelial cells in atherosclerosis: identifying C1 CXCL12+ ECs as key proliferative drivers for immunological precision therapeutics in atherosclerosis.

Front Immunol. 2025-5-12

[2]
Decoding multiple myeloma: single-cell insights into tumor heterogeneity, immune dynamics, and disease progression.

Front Immunol. 2025-5-8

[3]
IQGAP2 regulates blood-brain barrier immune dynamics.

iScience. 2025-2-11

[4]
Deciphering novel mitochondrial signatures: multi-omics analysis uncovers cross-disease markers and oligodendrocyte pathways in Alzheimer's disease and glioblastoma.

Front Aging Neurosci. 2025-2-13

[5]
The Endothelial Cell-Related Genes and Contribute to the Pathogenesis of Alzheimer's Disease by Modulating Peripheral Immunoinflammatory Responses.

Brain Sci. 2025-2-16

[6]
Integrating Bulk and Single-Cell Transcriptomic Data to Identify Ferroptosis-Associated Inflammatory Gene in Alzheimer's Disease.

J Inflamm Res. 2025-2-10

[7]
Single-cell sequencing reveals that AK5 inhibits apoptosis in AD oligodendrocytes by regulating the AMPK signaling pathway.

Mol Biol Rep. 2025-2-8

[8]
Single-cell RNA sequencing and immune microenvironment analysis reveal PLOD2-driven malignant transformation in cervical cancer.

Front Immunol. 2025-1-7

[9]
Single-cell analysis unveils cell subtypes of acral melanoma cells at the early and late differentiation stages.

J Cancer. 2025-1-1

[10]
The cellular signaling crosstalk between memory B cells and tumor cells in nasopharyngeal carcinoma cannot be overlooked: Their involvement in tumor progression and treatment strategy is significant.

J Cancer. 2025-1-1

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