Purpose <p>Hematopoietic stem cell transplantation (HSCT) depends on effective HSC mobilization with granulocyte colony-stimulating factor (G-CSF), though some allogeneic donors experience severe side effects. This study compares G-CSF and acute maximal exercise for HSC collection and cellular composition in 10 healthy family donors, examining links to donor fitness and recipient outcomes.</p> Methods <p>Ten donors (3 females; 40.8 (18.3) years) and their recipients (<i>n</i> = 8; 3 females; 47.5 (18.5) years) were enrolled. Donors completed cardiopulmonary exercise testing with blood samples taken pre- and post-exercise and on apheresis day for flow cytometric analysis. Recipients were followed up on day ~ 30 post-transplant.</p> Results <p>Exercise significantly increased circulating total CD34+ cells (1.76-fold (0.51), <i>p</i> = 0.002) and select progenitor subsets (CD34+CD45dim, 1.74-fold (0.56), <i>p</i> = 0.006; and CD34+CD38+CD133+, 1.60-fold (0.46), <i>p</i> = 0.013), while other subsets showed no significant change (<i>p</i> &gt; 0.05). Compared with post-exercise, apheresis resulted in markedly higher concentrations of total CD34+ cells (20.7-fold (9.7), <i>p</i> &lt; 0.001) and all measured subsets. The largest enrichments were observed in CD34+ CD38−CD133+ (52.7-fold (69.3) <i>p</i> = 0.005) and CD34+CD38+CD133+ (38.2-fold (17.0), <i>p</i> &lt; 0.001) populations. HSC collection at apheresis contained a 186.1-fold (72.3) elevation of immature granulocytes (<i>p</i> &lt; 0.001) compared to the acute exercise (1.5-fold (0.3)). The proportions of apoptotic CD34+&#xa0;cells and their subpopulations were similar post-exercise to apheresis (<i>p</i> &gt; 0.05). Donor CD34+CD38- cell number was significantly negatively associated with recipient engrafting CD34+CD45dimCD90+ cells/µl (<i>r</i>=-0.70, <i>p</i> = 0.05, <i>n</i> = 8).</p> Conclusion <p>Exercise might complement pharmacological mobilization by enhancing key HSC subgroups, improving collection quality, and supporting transplantation success; future research should evaluate combined approaches and the role of CRF in donor suitability and recipient outcomes.</p>

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Cellular profile of hematopoietic stem cells mobilized by exercise versus G-CSF in healthy related donors

  • Elias Siebold,
  • Laura Infanti,
  • Hans-Jürgen Gruber,
  • Gregor T. Stehle,
  • Debbie Maurer,
  • Egbert T. Ritter,
  • Michael Medinger,
  • Francesca Matteazzi,
  • Arno Schmidt-Trucksäss,
  • Andreas Holbro,
  • Julia M. Kröpfl

摘要

Purpose

Hematopoietic stem cell transplantation (HSCT) depends on effective HSC mobilization with granulocyte colony-stimulating factor (G-CSF), though some allogeneic donors experience severe side effects. This study compares G-CSF and acute maximal exercise for HSC collection and cellular composition in 10 healthy family donors, examining links to donor fitness and recipient outcomes.

Methods

Ten donors (3 females; 40.8 (18.3) years) and their recipients (n = 8; 3 females; 47.5 (18.5) years) were enrolled. Donors completed cardiopulmonary exercise testing with blood samples taken pre- and post-exercise and on apheresis day for flow cytometric analysis. Recipients were followed up on day ~ 30 post-transplant.

Results

Exercise significantly increased circulating total CD34+ cells (1.76-fold (0.51), p = 0.002) and select progenitor subsets (CD34+CD45dim, 1.74-fold (0.56), p = 0.006; and CD34+CD38+CD133+, 1.60-fold (0.46), p = 0.013), while other subsets showed no significant change (p > 0.05). Compared with post-exercise, apheresis resulted in markedly higher concentrations of total CD34+ cells (20.7-fold (9.7), p < 0.001) and all measured subsets. The largest enrichments were observed in CD34+ CD38−CD133+ (52.7-fold (69.3) p = 0.005) and CD34+CD38+CD133+ (38.2-fold (17.0), p < 0.001) populations. HSC collection at apheresis contained a 186.1-fold (72.3) elevation of immature granulocytes (p < 0.001) compared to the acute exercise (1.5-fold (0.3)). The proportions of apoptotic CD34+ cells and their subpopulations were similar post-exercise to apheresis (p > 0.05). Donor CD34+CD38- cell number was significantly negatively associated with recipient engrafting CD34+CD45dimCD90+ cells/µl (r=-0.70, p = 0.05, n = 8).

Conclusion

Exercise might complement pharmacological mobilization by enhancing key HSC subgroups, improving collection quality, and supporting transplantation success; future research should evaluate combined approaches and the role of CRF in donor suitability and recipient outcomes.