22–23 Jul 2026
Heidelberg Congress Center
Europe/Berlin timezone

Acute Exercise Preferentially Increases B-Cell-Derived Cell-Free DNA In Adults with Chronic Lymphocytic Leukaemia

23 Jul 2026, 11:45
1h 15m
Heidelberg Congress Center ( Heidelberg Congress Center )

Heidelberg Congress Center

Heidelberg Congress Center

Czernyring 20 69115 Heidelberg Germany
1 - Scientific Poster Poster Session

Speaker

David Bartlett

Description

Background. Elevated and impaired cell-free DNA (cfDNA) clearance are associated with increased tumour burden in chronic lymphocytic leukaemia (CLL). Although exercise has anti-tumour effects, the mechanisms underlying these effects are unclear. In healthy adults, acute exercise induces biphasic increases in cfDNA, followed by reductions upon completion. We aimed to understand the cfDNA response to acute exercise in patients with CLL.
Methods. Five treatment-naïve CLL (CLL: 65±11 years), five age- and sex-matched (OLD: 60±2 years) and seven young (YOUNG: 21±1 years) healthy adults completed a 30-minute high-intensity interval exercise session with blood taken before (PRE), immediately after (POST) and 30 minutes after (P30) exercise. We assessed complete blood counts (WBC, lymphocytes, monocytes, and neutrophils), while cfDNA in serum was assessed using RT-PCR for DNA fragments from neutrophils, lymphocytes, monocytes, and B-cells.
Results. As expected, immune cell Group x Time interactions were observed for counts of WBC (F=9.8, p<0.001, η²=.620), lymphocytes (F=6.6, p<0.001, η²=.524) and monocytes (F=3.6, p=0.020, η²=.373). These were characterised by all groups increasing immune cell counts from PRE to POST and returning to PRE levels at P30. CLL had ~8-10 times more monocytes and lymphocytes at each timepoint (all p<0.05). Lymphocyte cfDNA increases were characterised by CLL having 38.2±12% higher B-cell specific cfDNA at POST compared to YOUNG (p<0.001) and OLD (p<0.001). A group x time interaction was observed for neutrophil cfDNA (F=8.28, p<0.001, ŋ²=0.580) with similar increases PRE-to-POST in CLL and OLD (mean group diff.=12±14%, p=0.072) but higher expression at POST in the YOUNG compared to CLL (mean group diff.=38±14%, p=0.004).
Conclusion. Exercise elicits an exaggerated transient B-cell-derived cfDNA response in CLL, suggesting that exercise damages CLL cells. These cfDNA dynamics could support immune modulation and disease management in CLL. Further investigation is warranted.

Keywords

Leukaemia cfDNA; acute exercise; CLL;

Abstract submitters declaration yes
Conflict of Interest & Ethical Approval yes

Author

David Bartlett

Co-authors

Ellie Miles (University of Surrey) Eleanor Stratton (University of Surrey) Andrew Hulton (University of Surrey) Caitlin Jeary (University of Surrey) Long Li (University of Surrey) Barbara Fielding (University of Surrey) Uzma Zaheer (University of Surrey) Ralpn Manders (University of Surrey) Renata Walewska (University Hospitals Dorset) Sunil Iyengar (Haemato-Oncology Unit, Royal Marsden Hospital) Erik Hanson (Department of Exercise & Sport Science, University of North Carolina) Andrea Sitlinger (Department of Hematologic Malignancies and Cellular Therapies, Duke University)

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