Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Feb;35(2):e70020.
doi: 10.1111/sms.70020.

Effects of Exercise Training on the Bone Marrow Immune Microenvironment and Minimal Residual Disease in Multiple Myeloma Patients Following First-Line Treatment

Affiliations

Effects of Exercise Training on the Bone Marrow Immune Microenvironment and Minimal Residual Disease in Multiple Myeloma Patients Following First-Line Treatment

Polyxeni Spiliopoulou et al. Scand J Med Sci Sports. 2025 Feb.

Abstract

The purpose of the study was to investigate the effects of exercise training on the bone marrow immune microenvironment and on minimal residual disease of multiple myeloma patients who completed first-line induction treatment. Eight multiple myeloma patients underwent 5 months of exercise training along with standard medical treatment. Eight age- and sex-matched patients who received medical treatment only, served as controls. Before and after the intervention, white blood cells, red blood cells, and platelets, as well as the percentages of neutrophils, lymphocytes, monocytes, eosinophils, and basophils, were measured in the peripheral blood. Abnormal plasma cells, normal plasma cells, B cells, T cells, NK/NKT cells, monocytes, neutrophils, eosinophils, basophils, mast cells, myeloid progenitors, erythroid progenitors, and erythroblasts were assessed in the bone marrow. Exercise training increased the percentage of blood monocytes (mean difference 3.5% ± 2.6%; p = 0.006), while no change was detected in the control group. In the bone marrow, the CD27+ T cell subset increased (mean difference 18.2% ± 21.9%; p = 0.043) and the ratio of CD27-/CD27+ T lymphocytes decreased (pre: 1.06 ± 0.59; post: 0.76 ± 0.47; p = 0.049) in the exercise group, but remained unaltered in the control group. In conclusion, the study provides evidence that 5 months of exercise training can induce an increase in the percentage of activated T lymphocytes, as shown by the higher expression of the costimulatory CD27 marker. It also suggests that exercise-induced changes in the bone marrow microenvironment may be beneficial in the control of clonal cell proliferation.

Keywords: CD27 receptor; bone marrow immunity; exercise immunology; exercise oncology immunology; exercise training; minimal residual disease; multiple myeloma; sports medicine.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Percentages of erythroblasts, neutrophils, eosinophils, mast cells, monocytes, B cells, T cells, and NK/NKT cells on the bone marrow before (pre) and after (post) ~5 months of exercise training or control intervention in multiple myeloma patients after first‐line treatment. Values from the same patient are connected with a line. *p < 0.05.
FIGURE 2
FIGURE 2
Changes in CD27+ T and NK/NKT cell subsets, monocytes, and neutrophils, and CD27−/CD27+ ratios in the bone marrow before (pre) and after (post) ~5 months of exercise training or control intervention in multiple myeloma patients after first‐line treatment. Values from the same patient are connected with a line. *p < 0.05. IMiD, immunomodulatory drug; w/o, without.
FIGURE 3
FIGURE 3
Level of MRD before (pre) and after (post) ~5 months of exercise training or control intervention in multiple myeloma patients after first‐line treatment. Values from the same patient are connected with a line. MRD, minimal residual disease.

Similar articles

References

    1. Kumar S., Paiva B., Anderson K. C., et al., “International Myeloma Working Group Consensus Criteria for Response and Minimal Residual Disease Assessment in Multiple Myeloma,” Lancet Oncology 17 (2016): e328–e346. - PubMed
    1. Rajkumar S. V., Dimopoulos M. A., Palumbo A., et al., “International Myeloma Working Group Updated Criteria for the Diagnosis of Multiple Myeloma,” Lancet Oncology 15 (2014): e538–e548. - PubMed
    1. Rajkumar S. V. and Kumar S., “Multiple Myeloma: Diagnosis and Treatment,” Mayo Clinic Proceedings 91 (2016): 101–119. - PMC - PubMed
    1. Manier S., Sacco A., Leleu X., Ghobrial I. M., and Roccaro A. M., “Bone Marrow Microenvironment in Multiple Myeloma Progression,” BioMed Research International 2012 (2012): 157496. - PMC - PubMed
    1. Lopes R., Caetano J., Ferreira B., Barahona F., Carneiro E. A., and João C., “The Immune Microenvironment in Multiple Myeloma: Friend or Foe?,” Cancers 13 (2021): 625. - PMC - PubMed