Frontiers in Sports and Active Living (May 2023)

Acute exercise induces distinct quantitative and phenotypical T cell profiles in men with prostate cancer

  • Erik D. Hanson,
  • Erik D. Hanson,
  • Erik D. Hanson,
  • Erik D. Hanson,
  • Samy Sakkal,
  • Lauren C. Bates-Fraser,
  • Lauren C. Bates-Fraser,
  • Lauren C. Bates-Fraser,
  • Shadney Que,
  • Eunhan Cho,
  • Guillaume Spielmann,
  • Elif Kadife,
  • John A. Violet,
  • Claudio L. Battaglini,
  • Claudio L. Battaglini,
  • Claudio L. Battaglini,
  • Lee Stoner,
  • Lee Stoner,
  • David B. Bartlett,
  • Glenn K. McConell,
  • Alan Hayes,
  • Alan Hayes,
  • Alan Hayes

DOI
https://doi.org/10.3389/fspor.2023.1173377
Journal volume & issue
Vol. 5

Abstract

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BackgroundReduced testosterone levels can influence immune system function, particularly T cells. Exercise during cancer reduces treatment-related side effects and provide a stimulus to mobilize and redistribute immune cells. However, it is unclear how conventional and unconventional T cells (UTC) respond to acute exercise in prostate cancer survivors compared to healthy controls.MethodsAge-matched prostate cancer survivors on androgen deprivation therapy (ADT) and those without ADT (PCa) along with non-cancer controls (CON) completed ∼45 min of intermittent cycling with 3 min at 60% of peak power interspersed by 1.5 min of rest. Fresh, unstimulated immune cell populations and intracellular perforin were assessed before (baseline), immediately following (0 h), 2 h, and 24 h post-exercise.ResultsAt 0 h, conventional T cell counts increased by 45%–64% with no differences between groups. T cell frequency decreased by −3.5% for CD3+ and −4.5% for CD4+ cells relative to base at 0 h with CD8+ cells experiencing a delayed decrease of −4.5% at 2 h with no group differences. Compared to CON, the frequency of CD8+CD57+ cells was −18.1% lower in ADT. Despite a potential decrease in maturity, ADT increased CD8+perforin+ GMFI. CD3+Vα7.2+CD161+ counts, but not frequencies, increased by 69% post-exercise while CD3+CD56+ cell counts increased by 127% and were preferentially mobilized (+1.7%) immediately following the acute cycling bout. There were no UTC group differences. Cell counts and frequencies returned to baseline by 24 h.ConclusionFollowing acute exercise, prostate cancer survivors demonstrate normal T cell and UTC responses that were comparable to CON. Independent of exercise, ADT is associated with lower CD8+ cell maturity (CD57) and perforin frequency that suggests a less mature phenotype. However, higher perforin GMFI may attenuate these changes, with the functional implications of this yet to be determined.

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