Laboratory of Immunohematology, Division of Hematology, Department of Internal Medicine, Medical School, University of Patras, Patras, Greece.
Department of Respiratory Medicine, General Hospital of Pyrgos "Andreas Papandreou", Pyrgos, Greece.
Front Immunol. 2023 Jan 13;13:1009065. doi: 10.3389/fimmu.2022.1009065. eCollection 2022.
Marathon is a running event in which athletes must cover a distance of 42.195 km. In addition to participating in marathons, marathoners have incorporated extensive running into their lifestyle. In the present study, we investigated the effect of long-term strenuous exercise in the form of marathon running on the immune system.
METHODS & RESULTS: We collected peripheral blood samples from 37 male marathoners before/after a race and 37 age/sex/body mass index (BMI)-matched healthy sedentary controls. Hematological and biochemical tests revealed race-induced leukocytosis attributable to neutrophilia and significant increases in plasma lactate dehydrogenase (LDH), creatine phosphokinase (CPK), and cortisol concentrations. Phenotypic analysis of lymphocytes revealed race-induced significant decrease in the number of lymphocytes, memory helper T (Th) cells, naive, memory and activated cytotoxic T (Tc) cells, natural killer (NK), NKT, and B1 cells, and a significant increase in the number of activated Th and regulatory Th cells (Tregs). Compared with controls, marathoners maintained significantly lower levels of memory and activated Th cells and higher levels of activated Tc and B1 cells. Measurement of plasma cytokine levels revealed a pro-inflammatory cytokine polarization that increased after the race. Examination of gene expression of cytokines and Th-cell signature transcription factors in peripheral blood mononuclear cells revealed a significant decrease in tumor necrosis factor α (TNF-α) and interleukin (IL)-17, and a significant increase in IL-6, IL-10 and forkhead box P3 (FoxP3) after the race. Compared with controls, marathoners maintained significantly higher levels of TNF-α. Assessment of the suppressive capacity of Tregs in co-cultures of isolated effector Th cells and Tregs showed significantly increased suppressive capacity of marathoners' Tregs after the race.
Compared with controls, marathoners live with permanent changes in certain immune parameters. Marathoners exhibit a stable pro-inflammatory cytokine polarization that increases after the race and is counterbalanced by increased numbers of Tregs overexpressing FoxP3 and having increased suppressive capacity.
马拉松是一项运动员需完成 42.195 公里长跑的跑步项目。除了参加马拉松比赛,马拉松运动员还将大量跑步融入他们的生活方式。在本研究中,我们调查了以马拉松长跑形式进行的长期剧烈运动对免疫系统的影响。
我们收集了 37 名男性马拉松运动员比赛前后和 37 名年龄/性别/体重指数(BMI)匹配的健康久坐对照者的外周血样本。血液学和生化测试显示,比赛引起的白细胞增多归因于中性粒细胞增多和血浆乳酸脱氢酶(LDH)、肌酸磷酸激酶(CPK)和皮质醇浓度的显著升高。淋巴细胞表型分析显示,比赛引起的淋巴细胞、记忆辅助 T(Th)细胞、幼稚、记忆和激活细胞毒性 T(Tc)细胞、自然杀伤(NK)、NKT 和 B1 细胞数量显著减少,而激活的 Th 和调节性 Th 细胞(Tregs)数量显著增加。与对照组相比,马拉松运动员保持的记忆性和激活性 Th 细胞水平显著降低,而激活性 Tc 和 B1 细胞水平显著升高。测量血浆细胞因子水平显示,比赛后促炎细胞因子极化增加。外周血单个核细胞中细胞因子和 Th 细胞特征转录因子的基因表达检测显示,比赛后肿瘤坏死因子-α(TNF-α)和白细胞介素(IL)-17 显著减少,IL-6、IL-10 和叉头框 P3(FoxP3)显著增加。与对照组相比,马拉松运动员 TNF-α 水平显著升高。在分离的效应 Th 细胞和 Tregs 共培养物中评估 Tregs 的抑制能力显示,比赛后马拉松运动员的 Tregs 抑制能力显著增强。
与对照组相比,马拉松运动员的某些免疫参数存在永久性变化。马拉松运动员表现出稳定的促炎细胞因子极化,比赛后增加,并通过过度表达 FoxP3 且抑制能力增强的 Tregs 数量增加来平衡。