Acute exercise impacts AhR and PD-1 levels of CD8+ T-cells-Exploratory results from a randomized cross-over trial comparing endurance versus resistance exercise

Eur J Appl Physiol. 2021 Feb;121(2):637-644. doi: 10.1007/s00421-020-04552-w. Epub 2020 Nov 19.

Abstract

Purpose: The programmed cell death protein 1 (PD-1) has become a promising target in cancer immunotherapy. PD-1 expression of CD8+ T-cells may be increased via the exploitation of aryl hydrocarbon receptor (AhR) signaling with kynurenine (KYN) as a ligand. Since exercise affects KYN metabolism, we exploratory investigated the influence of acute exercise bouts on AhR and PD-1 levels of CD8+ T-cells.

Method: In this study, 24 healthy males (age: 24.6 ± 3.9 years; weight 83.9 ± 10.5 kg; height: 182.4 ± 6.2 cm) completed a single bout of endurance (EE) and resistance exercise (RE) in a randomly assigned order on separate days. Blood samples were drawn before (t0), after (t1), and 1 h after (t2) both conditions. T-cell populations, the level of cytoplasmic AhR, and surface PD-1 were assessed by flow cytometry.

Results: T-cell populations changed over time, indicated by an increase in the absolute numbers of CD3+ lymphocytes after EE (p < .001) and RE (p = .036) and in PD-1+ CD8+ T-cells after EE (p = .021). Proportions of T-cell populations changed only after EE (t0-t2: p = .029; t1-t2: p = .006). The level of cytoplasmic AhR decreased immediately after exercise in both exercise conditions (EE: p = .009; RE: p = .036). The level of surface PD-1 decreased 1 h after EE (p = .005).

Conclusion: We analyzed the level of surface PD-1 and cytoplasmic AhR following acute physical exercise for the first time. Especially EE was observed to impact both AhR and PD-1 levels, undermining its role as the AhR-PD-1 axis modulator. These results provide new insights into the impact of exercise on AhR-signaling, which could potentially be relevant for various chronic diseases.

Keywords: Acute exercise; AhR; Kynurenine; PD-1; T-cell.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • CD8-Positive T-Lymphocytes / metabolism*
  • CD8-Positive T-Lymphocytes / physiology*
  • Cross-Over Studies
  • Exercise / physiology*
  • Humans
  • Male
  • Physical Endurance / physiology*
  • Programmed Cell Death 1 Receptor / metabolism*
  • Receptors, Aryl Hydrocarbon / metabolism*
  • Resistance Training / methods
  • Signal Transduction / physiology
  • Young Adult

Substances

  • AHR protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Receptors, Aryl Hydrocarbon