TY - JOUR
T1 - Dynamics of circulating dendritic cells and cytokines after kidney transplantation - no effect of remote ischaemic conditioning
AU - Nielsen, Marie B
AU - Ravlo, Kristian
AU - Eijken, Marco
AU - Krogstrup, Nicoline V
AU - Svendsen, Morten Bue
AU - Abdel-Halim, Chadi
AU - Petersen, Mikkel Steen
AU - Birn, Henrik
AU - Oltean, Mihai
AU - Jespersen, Bente
AU - Møller, Bjarne K
N1 - This article is protected by copyright. All rights reserved.
PY - 2021/11
Y1 - 2021/11
N2 - 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 randomised CONTEXT study. Three circulating dendritic cell (DC) subtypes identified in peripheral blood from kidney transplant recipients (myeloid DCs, plasmacytoid DCs, and ILT3+ DCs) were measured at baseline, Day 1, Day 3, Day 5, one month, and three months after transplantation. We also quantified twenty-one cytokines at baseline, Day 1, Day 5, and three 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.
AB - 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 randomised CONTEXT study. Three circulating dendritic cell (DC) subtypes identified in peripheral blood from kidney transplant recipients (myeloid DCs, plasmacytoid DCs, and ILT3+ DCs) were measured at baseline, Day 1, Day 3, Day 5, one month, and three months after transplantation. We also quantified twenty-one cytokines at baseline, Day 1, Day 5, and three 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.
KW - cytokines
KW - dendritic cells
KW - immunology
KW - kidney transplantation
KW - remote ischaemic conditioning
U2 - 10.1111/cei.13658
DO - 10.1111/cei.13658
M3 - Journal article
C2 - 34473350
VL - 206
SP - 226
EP - 236
JO - Clinical and Experimental Immunology
JF - Clinical and Experimental Immunology
SN - 0009-9104
IS - 2
ER -