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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.

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/7ec2/9523253/1330f5a0ba5c/fcimb-12-990402-g001.jpg

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