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评估呼吸道病毒感染中免疫衰老 CD8 T 细胞的方法。

Method to Assess Immunosenescent CD8 T Cells in Respiratory Viral Infections.

机构信息

Department of Pediatrics, Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

Institute for Infection, Inflammation, and Immunity in Children (i4Kids), Pittsburgh, PA, USA.

出版信息

Methods Mol Biol. 2025;2857:33-43. doi: 10.1007/978-1-0716-4128-6_4.

DOI:10.1007/978-1-0716-4128-6_4
PMID:39348053
Abstract

Immunosenescence is a well-characterized phenomenon that occurs with increasing age in all immune and somatic cells. In order to best study immunosenescence, it is imperative to develop methods to accurately identify immunosenescent cells. Elderly patients are known to have impaired immune responses to respiratory viruses, and it is hypothesized that this is due, in part, to immunosenescent, terminally exhausted CD8 T cells. To test this hypothesis, we developed an aged mouse model and a flow cytometry protocol using the Cytek Aurora to assess the CD8 T-cell response during respiratory viral infection and identify immunosenescent CD8 T cells. This protocol and our aged mouse model have great potential to be incredibly valuable for future studies elucidating how to rejuvenate and possibly reverse immunosenescent CD8 T cells, which could improve the immune response to respiratory viruses in this at-risk population.

摘要

免疫衰老(Immunosenescence)是一种随着年龄增长而在所有免疫和体细胞中发生的特征明显的现象。为了能够最好地研究免疫衰老,开发准确识别免疫衰老细胞的方法是当务之急。众所周知,老年患者对呼吸道病毒的免疫反应受损,据推测,这部分是由于免疫衰老、终末衰竭的 CD8 T 细胞所致。为了验证这一假说,我们开发了一种老年小鼠模型和一种使用 Cytek Aurora 的流式细胞术方案,以评估呼吸道病毒感染过程中的 CD8 T 细胞反应,并鉴定免疫衰老的 CD8 T 细胞。该方案和我们的老年小鼠模型具有很大的潜力,对于未来阐明如何使免疫衰老的 CD8 T 细胞恢复活力并可能逆转的研究将具有非常重要的价值,这可能会改善该高危人群对呼吸道病毒的免疫反应。

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Method to Assess Immunosenescent CD8 T Cells in Respiratory Viral Infections.评估呼吸道病毒感染中免疫衰老 CD8 T 细胞的方法。
Methods Mol Biol. 2025;2857:33-43. doi: 10.1007/978-1-0716-4128-6_4.
2
Chronic alcohol increases CD8+ T-cell immunosenescence in simian immunodeficiency virus-infected rhesus macaques.慢性酒精会加剧感染猿猴免疫缺陷病毒的恒河猴体内CD8 + T细胞的免疫衰老。
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Aging and CD8+ T cell immunity to respiratory virus infections.衰老与CD8 + T细胞对呼吸道病毒感染的免疫
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The chemokine receptor CCR5 plays a key role in the early memory CD8+ T cell response to respiratory virus infections.趋化因子受体CCR5在呼吸道病毒感染早期记忆性CD8 + T细胞反应中起关键作用。
Immunity. 2008 Jul 18;29(1):101-13. doi: 10.1016/j.immuni.2008.05.011.
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Methods used to study respiratory virus infection.用于研究呼吸道病毒感染的方法。
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本文引用的文献

1
Terminally exhausted CD8 T cells contribute to age-dependent severity of respiratory virus infection.终末耗竭的CD8 T细胞导致呼吸道病毒感染的年龄依赖性严重程度。
Immun Ageing. 2023 Aug 1;20(1):40. doi: 10.1186/s12979-023-00365-5.
2
Human Metapneumovirus Reinfection in Aged Mice Recapitulates Increased Disease Severity in Elderly Humans Infected with Human Metapneumovirus.老年人中人类偏肺病毒再感染重现了老年人中人类偏肺病毒感染后疾病严重程度增加的现象。
Immunohorizons. 2023 Jun 1;7(6):398-411. doi: 10.4049/immunohorizons.2300026.
3
Neonatal Immune Responses to Respiratory Viruses.
新生儿对呼吸道病毒的免疫反应。
Front Immunol. 2022 Apr 14;13:863149. doi: 10.3389/fimmu.2022.863149. eCollection 2022.
4
Granzyme B: a double-edged sword in the response to influenza infection in vaccinated older adults.颗粒酶B:接种疫苗的老年人应对流感感染时的双刃剑。
Front Aging. 2021;2. doi: 10.3389/fragi.2021.753767. Epub 2021 Nov 11.
5
Novel HLA-B7-restricted human metapneumovirus epitopes enhance viral clearance in mice and are recognized by human CD8 T cells.新型 HLA-B7 限制性人类偏肺病毒表位增强小鼠体内病毒清除能力,并可被人类 CD8 T 细胞识别。
Sci Rep. 2021 Oct 21;11(1):20769. doi: 10.1038/s41598-021-00023-0.
6
Comprehensive Profiling of an Aging Immune System Reveals Clonal GZMK CD8 T Cells as Conserved Hallmark of Inflammaging.全面分析衰老免疫系统揭示克隆性 GZMK CD8 T 细胞是炎症衰老的保守标志。
Immunity. 2021 Jan 12;54(1):99-115.e12. doi: 10.1016/j.immuni.2020.11.005. Epub 2020 Dec 2.
7
Distinct Age-Related Epigenetic Signatures in CD4 and CD8 T Cells.CD4 和 CD8 T 细胞中独特的与年龄相关的表观遗传特征。
Front Immunol. 2020 Nov 11;11:585168. doi: 10.3389/fimmu.2020.585168. eCollection 2020.
8
High Levels of Eomes Promote Exhaustion of Anti-tumor CD8 T Cells.高水平的 Eomes 促进抗肿瘤 CD8 T 细胞耗竭。
Front Immunol. 2018 Dec 18;9:2981. doi: 10.3389/fimmu.2018.02981. eCollection 2018.
9
Inflammaging: a new immune-metabolic viewpoint for age-related diseases.慢性炎症:与年龄相关疾病的新免疫代谢观点。
Nat Rev Endocrinol. 2018 Oct;14(10):576-590. doi: 10.1038/s41574-018-0059-4.
10
Multiple Inhibitory Pathways Contribute to Lung CD8+ T Cell Impairment and Protect against Immunopathology during Acute Viral Respiratory Infection.多种抑制性途径导致肺部CD8 + T细胞功能受损,并在急性病毒性呼吸道感染期间预防免疫病理损伤。
J Immunol. 2016 Jul 1;197(1):233-43. doi: 10.4049/jimmunol.1502115. Epub 2016 Jun 3.