Dynamics of circulating dendritic cells and cytokines after kidney transplantation-No effect of remote ischaemic conditioning

Clin Exp Immunol. 2021 Nov;206(2):226-236. doi: 10.1111/cei.13658. Epub 2021 Sep 29.

Abstract

Inflammation resulting from ischaemia/reperfusion injury can cause kidney graft dysfunction, increase the risk of delayed graft function and possibly reduce long-term graft survival. Remote ischaemic conditioning may protect against ischaemia/reperfusion injury and mitigate the immunological response to the graft. We investigated the immunological effects of remote ischaemic conditioning on kidney transplantation from deceased donors in the randomized CONTEXT study. Three circulating dendritic cell (DC) subtypes identified in peripheral blood from kidney transplant recipients [myeloid DCs, plasmacytoid DCs and immunoglobulin-like transcript (ILT)3+ DCs] were measured at baseline, days 1, 3 and 5 and 1 and 3 months after transplantation. We also quantified 21 cytokines at baseline, days 1 and 5 and 3 months after transplantation. Neither DC counts nor cytokine levels differed between patients receiving remote ischaemic conditioning and controls; however, several parameters exhibited dynamic and parallel alterations in the two groups over time, reflecting the immunological response to the kidney transplantation and immunosuppression.

Trial registration: ClinicalTrials.gov NCT01395719.

Keywords: cytokines; dendritic cells; immunology; kidney transplantation; remote ischaemic conditioning.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell Count
  • Cytokines* / blood
  • Cytokines* / immunology
  • Dendritic Cells* / immunology
  • Dendritic Cells* / metabolism
  • Female
  • Humans
  • Ischemic Preconditioning*
  • Kidney Transplantation*
  • Male
  • Middle Aged

Substances

  • Cytokines

Associated data

  • ClinicalTrials.gov/NCT01395719