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衰老与免疫:古老的探戈舞。

Aging and immunity: the age-old tango.

作者信息

Fernández Maestre Inés, Harris Alexander S, Amor Corina

机构信息

Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.

Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA

出版信息

Genes Dev. 2025 Aug 1;39(15-16):948-974. doi: 10.1101/gad.352644.125.


DOI:10.1101/gad.352644.125
PMID:40436627
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12315898/
Abstract

The rising global demographic aging and the subsequent increase in the prevalence of age-related diseases highlight the need to understand aging biology. A key player in organismal aging is the immune system, which has broad systemic effects. On the one hand, immune aging involves the decline of hematopoietic stem cells and significant alterations in the functionality and composition of both innate and adaptive immunity. On the other hand, the aged immune system contributes to chronic inflammation and disrupted tissue homeostasis, thereby driving systemic aging processes. In this review, we examine the close interaction between aging and the immune system and discuss emerging therapeutic strategies aimed at modulating immune function to mitigate age-related pathologies.

摘要

全球人口老龄化加剧以及随之而来的与年龄相关疾病患病率的上升,凸显了理解衰老生物学的必要性。机体衰老的一个关键因素是免疫系统,它具有广泛的全身效应。一方面,免疫衰老涉及造血干细胞的衰退以及固有免疫和适应性免疫在功能和组成上的显著改变。另一方面,衰老的免疫系统会导致慢性炎症和组织稳态破坏,从而推动全身衰老进程。在这篇综述中,我们研究了衰老与免疫系统之间的密切相互作用,并讨论了旨在调节免疫功能以减轻与年龄相关病理状况的新兴治疗策略。

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本文引用的文献

[1]
Cardiolipin-mimic lipid nanoparticles without antibody modification delivered senolytic in vivo CAR-T therapy for inflamm-aging.

Cell Rep Med. 2025-7-15

[2]
Elevated mitochondrial membrane potential is a therapeutic vulnerability in Dnmt3a-mutant clonal hematopoiesis.

Nat Commun. 2025-4-16

[3]
Single-cell immune aging clocks reveal inter-individual heterogeneity during infection and vaccination.

Nat Aging. 2025-4

[4]
Clonal dynamics and somatic evolution of haematopoiesis in mouse.

Nature. 2025-5

[5]
Reducing functionally defective old HSCs alleviates aging-related phenotypes in old recipient mice.

Cell Res. 2025-1

[6]
A chimeric peptide promotes immune surveillance of senescent cells in injury, fibrosis, tumorigenesis and aging.

Nat Aging. 2025-1

[7]
Plasma protein-based organ-specific aging and mortality models unveil diseases as accelerated aging of organismal systems.

Cell Metab. 2025-1-7

[8]
Targeting immunosenescence for improved tumor immunotherapy.

MedComm (2020). 2024-10-28

[9]
Senescence landscape in the liver following sepsis and senolytics as potential therapeutics.

Aging Cell. 2025-1

[10]
Age-associated imbalance in immune cell regeneration varies across individuals and arises from a distinct subset of stem cells.

Cell Mol Immunol. 2024-12

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