CD28
CD8型
细胞毒性T细胞
趋化因子受体
免疫学
免疫系统
趋化因子
T细胞
T细胞受体
生物
流式细胞术
CCL5
受体
CXCR3型
医学
白细胞介素2受体
趋化因子受体CCR5
细胞生物学
白细胞介素21
CD3型
受体表达
细胞
炎症
间歇训练
ZAP70型
自然杀伤性T细胞
C-C趋化因子受体6型
趋化因子受体
内科学
作者
Katharina Leuchte,Thy Viet Luu,Sara Fresnillo Saló,Kasper Madsen,Lise Heide-Ottosen,Signe K. Skadborg,Janine Kemming,Morten Orebo Holmström,Hongjin Chen,Lars Rønn Olsen,Anders Vinther,Mads Hald Andersen,Sine Reker Hadrup,thor Straten Per,Gitte Holmen Olofsson
标识
DOI:10.3389/fimmu.2025.1739657
摘要
Introduction Physical activity induces rapid and selective leukocyte mobilization. Among the most responsive cell types to high-intensity exercise are CD8 + T cells, key effectors of immune defense against infected cells and cancer. However, comprehensive profiling of acute high-intensity interval training (HIIT)-induced modulation of the CD8 + T cell compartment remains lacking. Methods We assessed the effects of a supervised, group-based HIIT session on the CD8+ T cell compartment in 23 healthy participants. Blood was collected at baseline, immediately post-exercise (ex02), and one hour post-exercise (ex60). CD8 + T cells were analyzed for virus peptide reactivity using DNA-barcoded peptide-MHC multimer staining targeting 250 peptides. Differentiation status, chemokine receptor expression, and ligand regulation were assessed by flow cytometry and Olink proteomics, and finally, associations between individual characteristics and CD8 + T cell mobilization were analyzed. Results A single HIIT bout induced robust CD8 + T cell mobilization followed by substantial egress, which were consistent across fitness levels, body composition and age. Circulating virus-reactive T cells significantly increased in peripheral blood in response to exercise across virus types, including EBV-, SARS-CoV-2- and CMV-specific T cells. HIIT modulated chemokine receptor profiles, and memory subsets were reorganized, reducing terminally differentiated and CD57 + , PD-1 + , and CD28 neg cells at ex60 post-exercise. Notably, catecholamines NE and EPI peaked post-exercise, and NE was selectively associated with CD8 + T cell mobilization. Discussion In conclusion, acute HIIT mobilizes functional, virus-reactive CD8 + T cells with features indicative of enhanced migratory and activation potential, supporting translational use from tumor immunology to infectious disease. The study is registered at clinicaltrials.gov (NCT05826496).
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