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衰老过程中的免疫系统调节:分子机制和治疗靶点。

Immune system modulation in aging: Molecular mechanisms and therapeutic targets.

机构信息

Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados, Instituto Politécnico Nacional, Ciudad de México, Mexico.

Departamento de Bioingeniería, Escuela de Ingeniería y Ciencias, Tecnologico de Monterrey, Ciudad de México, Mexico.

出版信息

Front Immunol. 2022 Dec 15;13:1059173. doi: 10.3389/fimmu.2022.1059173. eCollection 2022.


DOI:10.3389/fimmu.2022.1059173
PMID:36591275
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9797513/
Abstract

The function of the immune system declines during aging, compromising its response against pathogens, a phenomenon termed as "immunosenescence." Alterations of the immune system undergone by aged individuals include thymic involution, defective memory T cells, impaired activation of naïve T cells, and weak memory response. Age-linked alterations of the innate immunity comprise perturbed chemotactic, phagocytic, and natural killing functions, as well as impaired antigen presentation. Overall, these alterations result in chronic low-grade inflammation (inflammaging) that negatively impacts health of elderly people. In this review, we address the most relevant molecules and mechanisms that regulate the relationship between immunosenescence and inflammaging and provide an updated description of the therapeutic strategies aimed to improve immunity in aged individuals.

摘要

免疫系统的功能随着年龄的增长而下降,使其对病原体的反应受到损害,这种现象被称为“免疫衰老”。老年人的免疫系统发生的改变包括胸腺萎缩、记忆 T 细胞缺陷、幼稚 T 细胞激活受损以及记忆反应减弱。先天免疫的年龄相关改变包括趋化、吞噬和自然杀伤功能紊乱,以及抗原呈递受损。总的来说,这些改变导致慢性低度炎症(炎症衰老),对老年人的健康产生负面影响。在这篇综述中,我们讨论了调节免疫衰老和炎症衰老之间关系的最相关分子和机制,并对旨在改善老年人免疫功能的治疗策略进行了更新描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/9797513/574a6d1d6806/fimmu-13-1059173-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/9797513/574a6d1d6806/fimmu-13-1059173-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/9797513/574a6d1d6806/fimmu-13-1059173-g001.jpg

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Immune system modulation in aging: Molecular mechanisms and therapeutic targets.

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本文引用的文献

[1]
Protects against Hyperlipidemia by Inhibiting Oxidative Stress and Inflammation through Nrf2/NF-κB Signaling in High Fat Diet Fed Mice.

Nutrients. 2022-8-24

[2]
Hypoxia in Aging and Aging-Related Diseases: Mechanism and Therapeutic Strategies.

Int J Mol Sci. 2022-7-25

[3]
Long-term caloric restriction ameliorates T cell immunosenescence in mice.

Mech Ageing Dev. 2022-9

[4]
Centenarians Alleviate Inflammaging by Changing the Ratio and Secretory Phenotypes of T Helper 17 and Regulatory T Cells.

Front Pharmacol. 2022-6-2

[5]
Developmental dynamics of two bipotent thymic epithelial progenitor types.

Nature. 2022-6

[6]
The mTOR inhibitor Rapamycin protects from premature cellular senescence early after experimental kidney transplantation.

PLoS One. 2022

[7]
Interconnections between Inflammageing and Immunosenescence during Ageing.

Cells. 2022-1-21

[8]
Rapamycin, Acarbose and 17α-estradiol share common mechanisms regulating the MAPK pathways involved in intracellular signaling and inflammation.

Immun Ageing. 2022-2-1

[9]
How Immunosenescence and Inflammaging May Contribute to Hyperinflammatory Syndrome in COVID-19.

Int J Mol Sci. 2021-11-21

[10]
Mechanisms underpinning poor antibody responses to vaccines in ageing.

Immunol Lett. 2022-1

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