Respiratory Diseases Group, Respiratory Service, La Paz University Hospital, IdiPAZ, Madrid, Spain.
Biomedical Research Networking Centre on Respiratory Diseases (CIBERES), Madrid, Spain.
Am J Physiol Lung Cell Mol Physiol. 2024 Oct 1;327(4):L464-L472. doi: 10.1152/ajplung.00151.2024. Epub 2024 Aug 6.
Chronic obstructive pulmonary disease (COPD) is regarded as an accelerated-age disease in which chronic inflammation, maladaptive immune responses, and senescence cell burden coexist. Accordingly, cellular senescence has emerged as a potential mechanism involved in COPD pathophysiology. In this study, 25 stable patients with COPD underwent a daily physical activity promotion program for 6 mo. We reported that increase of physical activity was related to a reduction of the senescent cell burden in circulating lymphocytes of patients with COPD. Senescent T-lymphocyte population, characterized by absence of surface expression of CD28, was reduced after physical activity intervention, and the reduction was associated to the increase of physical activity level. In addition, the mRNA expression of cyclin-dependent kinase inhibitors, a hallmark of cell senescence, was reduced and, in accordance, the proliferative capacity of lymphocytes was improved postintervention. Moreover, we observed an increase in functionality in T cells from patients after intervention, including improved markers of activation, enhanced cytotoxicity, and altered cytokine secretions in response to viral challenge. Lastly, physical activity intervention reduced the potential of lymphocytes' secretome to induce senescence in human primary fibroblasts. In conclusion, our study provides, for the first time, evidence of the potential of physical activity intervention in patients with COPD to reduce the senescent burden in circulating immune cells. For the first time, we identified in patients with COPD a relation between physical activity intervention with respiratory function improvement and cellular senescence burden in lymphocytes that improved the T cell functionality and proliferative capacity of patients. In addition, our experiments highlight the possible impact of T-cell senescence in other cell types which could be related to some of the clinical lung complications observed in COPD.
慢性阻塞性肺疾病(COPD)被认为是一种加速衰老的疾病,其中慢性炎症、适应性免疫反应和衰老细胞负担并存。因此,细胞衰老已成为 COPD 病理生理学中涉及的潜在机制。在这项研究中,25 名稳定的 COPD 患者接受了为期 6 个月的日常体力活动促进计划。我们报告说,体力活动的增加与 COPD 患者循环淋巴细胞中衰老细胞负担的减少有关。衰老 T 淋巴细胞群体的特征是缺乏表面表达 CD28,在体力活动干预后减少,并且减少与体力活动水平的增加有关。此外,细胞衰老的标志 cyclin 依赖性激酶抑制剂的 mRNA 表达减少,并且淋巴细胞的增殖能力在干预后得到改善。此外,我们观察到干预后患者 T 细胞的功能增加,包括改善的激活标志物、增强的细胞毒性以及对病毒挑战的细胞因子分泌的改变。最后,体力活动干预减少了淋巴细胞分泌组诱导人原代成纤维细胞衰老的潜力。总之,我们的研究首次提供了证据,证明 COPD 患者的体力活动干预有可能减轻循环免疫细胞中的衰老负担。我们首次在 COPD 患者中确定了体力活动干预与呼吸功能改善和淋巴细胞中细胞衰老负担之间的关系,改善了患者的 T 细胞功能和增殖能力。此外,我们的实验强调了 T 细胞衰老对其他细胞类型的可能影响,这可能与 COPD 中观察到的一些临床肺部并发症有关。