• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

心理应激会在肺部产生免疫抑制环境,增加老年小鼠感染的易感性。

Psychological stress creates an immune suppressive environment in the lung that increases susceptibility of aged mice to infection.

机构信息

Department of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, United States.

Host Pathogen Interactions Program, Texas Biomedical Research Institute, San Antonio, TX, United States.

出版信息

Front Cell Infect Microbiol. 2022 Sep 16;12:990402. doi: 10.3389/fcimb.2022.990402. eCollection 2022.

DOI:10.3389/fcimb.2022.990402
PMID:36189368
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9523253/
Abstract

Age is a major risk factor for chronic infections, including tuberculosis (TB). Elderly TB patients also suffer from elevated levels of psychological stress. It is not clear how psychological stress impacts immune response to ( In this study, we used social disruption stress (SDR) to investigate effects of psychological stress in young and old mice. Unexpectedly, we found that SDR suppresses lung inflammation in old mice as evidenced by lower pro-inflammatory cytokine levels in bronchial lavage fluid and decreased cytokine mRNA expression by alveolar macrophages. To investigate effects of stress on infection, mice were subjected to SDR and then infected with . As previously reported, old mice were better at controlling infection at 30 days than young mice. This control was transient as CFUs at 60 days were higher in old control mice compared to young mice. Consistently, SDR significantly increased growth at 60 days in old mice compared to young mice. In addition, SDR in old mice resulted in accumulation of IL-10 mRNA and decreased IFN-γ mRNA at 60 days. Also, confocal microscopy of lung sections from old SDR mice showed increased number of CD4 T cells which express LAG3 and CD49b, markers of IL-10 secreting regulatory T cells. Further, we also demonstrated that CD4 T cells from old SDR mice express IL-10. Thus, we conclude that psychological stress in old mice prior to infection, increases differentiation of IL-10 secreting T cells, which over time results in loss of control of the infection.

摘要

年龄是慢性感染(包括肺结核)的一个主要危险因素。老年肺结核患者还承受着更高水平的心理压力。目前尚不清楚心理压力如何影响对 的免疫反应。在这项研究中,我们使用社交扰乱应激(SDR)来研究心理应激对年轻和老年小鼠的影响。出乎意料的是,我们发现 SDR 抑制了老年小鼠的肺部炎症,支气管灌洗液中的促炎细胞因子水平较低,肺泡巨噬细胞中的细胞因子 mRNA 表达降低。为了研究应激对 感染的影响,将小鼠进行 SDR 处理,然后感染 。如前所述,老年小鼠在 30 天时比年轻小鼠更能控制感染。这种控制是短暂的,因为 60 天时老年对照小鼠的 CFU 高于年轻小鼠。同样,与年轻小鼠相比,SDR 显著增加了老年小鼠在 60 天时的 生长。此外,老年 SDR 小鼠在 60 天时 IL-10 mRNA 的积累增加,IFN-γ mRNA 减少。此外,来自老年 SDR 小鼠的肺组织切片的共聚焦显微镜显示,表达 LAG3 和 CD49b 的 CD4 T 细胞数量增加,这些标志物是分泌 IL-10 的调节性 T 细胞。此外,我们还证明了老年 SDR 小鼠的 CD4 T 细胞表达 IL-10。因此,我们得出结论,感染前老年小鼠的心理应激增加了分泌 IL-10 的 T 细胞的分化,随着时间的推移,导致感染失控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/b2242d40d613/fcimb-12-990402-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/1330f5a0ba5c/fcimb-12-990402-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/5a46214dcf0d/fcimb-12-990402-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/727fc7b64733/fcimb-12-990402-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/c7ee9f1b2639/fcimb-12-990402-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/e04738f0bf94/fcimb-12-990402-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/bda0b9111b0a/fcimb-12-990402-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/57a3b3ab4c1c/fcimb-12-990402-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/b2242d40d613/fcimb-12-990402-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/1330f5a0ba5c/fcimb-12-990402-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/5a46214dcf0d/fcimb-12-990402-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/727fc7b64733/fcimb-12-990402-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/c7ee9f1b2639/fcimb-12-990402-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/e04738f0bf94/fcimb-12-990402-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/bda0b9111b0a/fcimb-12-990402-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/57a3b3ab4c1c/fcimb-12-990402-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec2/9523253/b2242d40d613/fcimb-12-990402-g008.jpg

相似文献

1
Psychological stress creates an immune suppressive environment in the lung that increases susceptibility of aged mice to infection.心理应激会在肺部产生免疫抑制环境,增加老年小鼠感染的易感性。
Front Cell Infect Microbiol. 2022 Sep 16;12:990402. doi: 10.3389/fcimb.2022.990402. eCollection 2022.
2
T Cell-Derived IL-10 Impairs Host Resistance to Infection.T细胞衍生的白细胞介素-10会损害宿主对感染的抵抗力。
J Immunol. 2017 Jul 15;199(2):613-623. doi: 10.4049/jimmunol.1601340. Epub 2017 Jun 5.
3
Protection against Mycobacterium tuberculosis infection offered by a new multistage subunit vaccine correlates with increased number of IFN-γ+ IL-2+ CD4+ and IFN-γ+ CD8+ T cells.一种新型多阶段亚单位疫苗提供的针对结核分枝杆菌感染的保护作用与IFN-γ+ IL-2+ CD4+和IFN-γ+ CD8+ T细胞数量增加相关。
PLoS One. 2015 Mar 30;10(3):e0122560. doi: 10.1371/journal.pone.0122560. eCollection 2015.
4
Mycobacterium tuberculosis multi-drug-resistant strain M induces IL-17 IFNγ CD4 T cell expansion through an IL-23 and TGF-β-dependent mechanism in patients with MDR-TB tuberculosis.结核分枝杆菌多重耐药菌株M通过IL-23和TGF-β依赖机制诱导耐多药结核病患者的IL-17 IFNγ CD4 T细胞扩增。
Clin Exp Immunol. 2017 Jan;187(1):160-173. doi: 10.1111/cei.12873. Epub 2016 Nov 2.
5
IL-4 subverts mycobacterial containment in -infected human macrophages.IL-4 颠覆了感染人类巨噬细胞中的分枝杆菌控制。
Eur Respir J. 2019 Aug 8;54(2). doi: 10.1183/13993003.02242-2018. Print 2019 Aug.
6
Altered monocyte phenotypes but not impaired peripheral T cell immunity may explain susceptibility of the elderly to develop tuberculosis.改变的单核细胞表型,但未受损的外周 T 细胞免疫可能解释老年人易患结核病的原因。
Exp Gerontol. 2018 Oct 1;111:35-44. doi: 10.1016/j.exger.2018.06.029. Epub 2018 Jul 3.
7
Protection against an aerogenic Mycobacterium tuberculosis infection in BCG-immunized and DNA-vaccinated mice is associated with early type I cytokine responses.卡介苗免疫和DNA疫苗接种小鼠对气源性结核分枝杆菌感染的保护作用与早期I型细胞因子反应有关。
Vaccine. 2006 Apr 24;24(17):3522-9. doi: 10.1016/j.vaccine.2006.02.005. Epub 2006 Feb 20.
8
Role of tissue factor in Mycobacterium tuberculosis-induced inflammation and disease pathogenesis.组织因子在结核分枝杆菌诱导的炎症和疾病发病机制中的作用。
PLoS One. 2014 Dec 2;9(12):e114141. doi: 10.1371/journal.pone.0114141. eCollection 2014.
9
Prolonged B-Lymphocyte-Mediated Immune and Inflammatory Responses to Tuberculosis Infection in the Lungs of TB-Resistant Mice.耐结核感染小鼠肺部结核分枝杆菌感染引起的 B 淋巴细胞介导的免疫和炎症反应持续存在。
Int J Mol Sci. 2023 Jan 6;24(2):1140. doi: 10.3390/ijms24021140.
10
IL-37 Expression is Upregulated in Patients with Tuberculosis and Induces Macrophages Towards an M2-like Phenotype.白细胞介素-37在结核病患者中表达上调,并诱导巨噬细胞向M2样表型转变。
Scand J Immunol. 2015 Oct;82(4):370-9. doi: 10.1111/sji.12326.

引用本文的文献

1
CD4 Effective Memory T Cell Markers GBP2 and LAG3 Are Risk Factors for PTB and COVID-19 Infection: A Study Integrating Single-Cell Expression Quantitative Trait Locus and Mendelian Randomization Analyses.CD4 有效记忆 T 细胞标志物 GBP2 和 LAG3 是 PTB 和 COVID-19 感染的风险因素:一项整合单细胞表达数量性状基因座和孟德尔随机化分析的研究。
Int J Mol Sci. 2024 Sep 16;25(18):9971. doi: 10.3390/ijms25189971.

本文引用的文献

1
SARS-CoV-2 and COVID-19 in older adults: what we may expect regarding pathogenesis, immune responses, and outcomes.老年人中的 SARS-CoV-2 和 COVID-19:关于发病机制、免疫反应和结局,我们可能会有哪些预期。
Geroscience. 2020 Apr;42(2):505-514. doi: 10.1007/s11357-020-00186-0. Epub 2020 Apr 10.
2
Identification of an Increased Alveolar Macrophage Subpopulation in Old Mice That Displays Unique Inflammatory Characteristics and Is Permissive to Infection.鉴定老年小鼠中一种具有独特炎症特征且易于感染的肺泡巨噬细胞亚群。
J Immunol. 2019 Oct 15;203(8):2252-2264. doi: 10.4049/jimmunol.1900495. Epub 2019 Sep 11.
3
Effect of Mycobacterium tuberculosis Enhancement of Macrophage P-Glycoprotein Expression and Activity on Intracellular Survival During Antituberculosis Drug Treatment.
结核分枝杆菌增强巨噬细胞 P-糖蛋白表达和活性对抗结核药物治疗期间细胞内存活的影响。
J Infect Dis. 2019 Nov 6;220(12):1989-1998. doi: 10.1093/infdis/jiz405.
4
The Immunobiology of the Interleukin-12 Family: Room for Discovery.白细胞介素-12 家族的免疫生物学:探索的空间。
Immunity. 2019 Apr 16;50(4):851-870. doi: 10.1016/j.immuni.2019.03.011.
5
The Biology of T Regulatory Type 1 Cells and Their Therapeutic Application in Immune-Mediated Diseases.调节性 T 细胞 1 型的生物学特性及其在免疫介导性疾病中的治疗应用。
Immunity. 2018 Dec 18;49(6):1004-1019. doi: 10.1016/j.immuni.2018.12.001.
6
ADGRE1 (EMR1, F4/80) Is a Rapidly-Evolving Gene Expressed in Mammalian Monocyte-Macrophages.ADGRE1(EMR1,F4/80)是一种在哺乳动物单核细胞-巨噬细胞中迅速表达的基因。
Front Immunol. 2018 Oct 1;9:2246. doi: 10.3389/fimmu.2018.02246. eCollection 2018.
7
The β2-adrenergic receptor controls inflammation by driving rapid IL-10 secretion.β2 肾上腺素能受体通过驱动快速分泌白细胞介素 10 来控制炎症。
Brain Behav Immun. 2018 Nov;74:176-185. doi: 10.1016/j.bbi.2018.09.004. Epub 2018 Sep 5.
8
Tuberculosis in the elderly: Why inflammation matters.老年人结核病:炎症为何重要。
Exp Gerontol. 2018 May;105:32-39. doi: 10.1016/j.exger.2017.12.021. Epub 2017 Dec 26.
9
Reciprocal Expression of IL-35 and IL-10 Defines Two Distinct Effector Treg Subsets that Are Required for Maintenance of Immune Tolerance.IL-35 和 IL-10 的相互表达定义了两个不同的效应性 Treg 亚群,它们是维持免疫耐受所必需的。
Cell Rep. 2017 Nov 14;21(7):1853-1869. doi: 10.1016/j.celrep.2017.10.090.
10
T Cell-Derived IL-10 Impairs Host Resistance to Infection.T细胞衍生的白细胞介素-10会损害宿主对感染的抵抗力。
J Immunol. 2017 Jul 15;199(2):613-623. doi: 10.4049/jimmunol.1601340. Epub 2017 Jun 5.