Human immune cell mobilization during exercise: effect of IL-6 receptor blockade

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

New Findings: What is the central question of this study? Does blockade of the IL-6 receptor by tocilizumab inhibit immune cell mobilization to the blood stream in humans during an acute bout of exercise? What is the main finding and its importance? Blockade of IL-6 receptor signalling by tocilizumab attenuates mobilization of NK cells and dendritic cells to the blood stream during exercise. This implies an inhibitory effect of tocilizumab on the innate immune response to physical stress, which could be considered in clinical settings. Abstract: Immune cells are recruited from their storage organs and the endothelial walls to the blood stream in response to physiological stress. This is essential for the recognition and clearing of infected, transformed or damaged cells. One of the most potent stimuli to recruit immune cells to the circulation is exercise. Accordingly, exercise has proven beneficial in disease settings, such as cancer and diabetes. Interleukin-6 (IL-6) is released from contracting skeletal muscle in response to exercise, and rodent studies have established a link between exercise-induced IL-6 and recruitment of natural killer (NK) cells. Whether exercise-induced IL-6 is involved in regulating NK cell mobilization in humans is unclear. This study explored the effect of IL-6 receptor blockade on immune cell mobilization during an acute bout of exercise in humans. In a randomized, placebo-controlled clinical study, abdominally obese humans receiving placebo infusions or tocilizumab infusions performed an acute bout of exercise before and after the intervention. Immune cell recruitment was measured by flow cytometry. IL-6 receptor blockade attenuated the increase of NK cells by 53% (mean difference −0.49 (95% CI: −0.89 to −0.08) × 109 cells L−1, P < 0.001) and dendritic cells by 66% (mean difference −0.14 (95% CI: −0.28 to 0.010) נ109 cells L−1, P < 0.001) induced by an acute bout of exercises. No changes were observed for T cells, monocytes and neutrophils. Treatments which interact with the exercise-mediated immune surveillance provide relevant clinical information in pursuing the ‘exercise as medicine’ concept.

OriginalsprogEngelsk
TidsskriftExperimental Physiology
Vol/bind105
Udgave nummer12
Sider (fra-til)2086-2098
Antal sider13
ISSN0958-0670
DOI
StatusUdgivet - 2020

Bibliografisk note

Funding Information:
We thank Anne‐Kristine Lundby and Lene Foged for assistance with catecholamine analyses by radioimmune‐assay. The Centre for Physical Activity Research (CFAS) is supported by a grant from TrygFonden (grant ID 101390 and 20045), and the Centre of Inflammation and Metabolism (CIM) is a member of DD2 – the Danish Centre for Strategic Research in Type 2 Diabetes (the Danish Council for Strategic Research, grant no. 09‐067009 and 09‐075724). L.L.L. was partly financed by a grant from the Danish Diabetes Academy, which is supported by the Novo Nordisk Foundation. R.H.C. was supported by the Danish Heart Foundation (grant ID 16‐R107‐A6704‐22970). M.L.B. and T.S. were supported by the Lundbeck Foundation (grant IDs R230‐2016‐3196 and R238‐2016‐2821, respectively). S.H., A.S.W.N., P.Ø.J., R.K.M. and H.E. did not receive further funding for this study.

Publisher Copyright:
© 2020 The Authors. Experimental Physiology © 2020 The Physiological Society

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