Exercise-induced cytokine changes in antigen stimulated whole-blood cultures compared to serum

J Immunol Methods. 2017 Jan:440:58-66. doi: 10.1016/j.jim.2016.11.007. Epub 2016 Nov 19.

Abstract

Strenuous exercise is followed by an elevation of many cytokines with inflammation regulating properties. Since most cytokines act at pico- or nanomolar concentrations many investigations failed to detect their concentrations in vivo. Hence, the aim of this study was to evaluate the significance of cytokine measurements (IL-1β, TNF-α, IL-1ra, IL-6, CCL2 and CXCL8) in a stimulated whole-blood culture (sWBC) compared to serum with respect to their exercise-induced kinetics and detection rates. 40 male volunteers (age: 25,5±4,3years, BMI: 24,00±2,24, VO2peak: 46,9±4,1mL/kg×min) performed 60min of intensive bicycle exercise (80% VO2peak). Blood samples were taken before and for up to 24h after exercise. All cytokines were determined by a multiplex ELISA. There were weak to moderate correlations between cytokines in sWBC and serum. While exercise did not affect pro-inflammatory cytokines in serum, in sWBC only IL-1β was increased 1.2-fold at 3h (p<0,05). All other cytokines increased both in sWBC and serum. The detection rate was superior in sWBC vs serum for most cytokines. Exercise-induced cytokine kinetics in sWBC do not reflect systemic changes. Both approaches provide a synergistic insight into inflammatory processes on the cytokine level.

Keywords: Cytokines; Exercise; Inflammation; Whole-blood culture.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Antigens / immunology*
  • Bicycling
  • Blood Cells / immunology*
  • Blood Cells / metabolism
  • Blood Chemical Analysis / methods*
  • Cells, Cultured
  • Cytokines / blood*
  • Enzyme-Linked Immunosorbent Assay
  • Exercise / physiology*
  • Flow Cytometry
  • Humans
  • Inflammation Mediators / blood*
  • Kinetics
  • Leukocyte Count
  • Male
  • Prospective Studies
  • Reproducibility of Results
  • Serum / immunology*
  • Specimen Handling / methods*
  • Up-Regulation
  • Young Adult

Substances

  • Antigens
  • Cytokines
  • Inflammation Mediators