Abstract

Donor organ shortage still remains a serious obstacle for the access of wait-list patients to kidney transplantation, the best treatment for End-Stage Kidney Disease (ESKD). To expand the number of transplants, the use of lower quality organs from older ECD or DCD donors has become an established routine but at the price of increased incidence of Primary Non-Function, Delay Graft Function and lower-long term graft survival. In the last years, several improvements have been made in the field of renal transplantation from surgical procedure to preservation strategies. To improve renal outcomes, research has focused on development of innovative and dynamic preservation techniques, in order to assess graft function and promote regeneration by pharmacological intervention before transplantation. This review provides an overview of the current knowledge of these new preservation strategies by machine perfusions and pharmacological interventions at different timing possibilities: in the organ donor, ex-vivo during perfusion machine reconditioning or after implementation in the recipient. We will report therapies as anti-oxidant and anti-inflammatory agents, senolytics agents, complement inhibitors, HDL, siRNA and H2S supplementation. Renal delivery of pharmacologic agents during preservation state provides a window of opportunity to treat the organ in an isolated manner and a crucial route of administration. Even if few studies have been reported of transplantation after ex-vivo drugs administration, targeting the biological pathway associated to kidney failure (i.e. oxidative stress, complement system, fibrosis) might be a promising therapeutic strategy to improve the quality of various donor organs and expand organ availability.

Highlights

  • Kidney transplantation represents the best treatment for patient with End-Stage Kidney Disease (ESKD) [1]

  • Bang et al investigated whether Remote ischemic preconditioning (RIPC) performed in living kidney donors using a blood pressure cuff placed on upper arm (3 cycles of inflation to 200mmHg for 5 minutes followed by deflation of the cuff for 5 minutes) could improve kidney function and outcomes in both donors and recipients; serum creatinine levels for donors at discharge was significantly lower in donors who received RIPC, while no significant difference in serum creatinine, eGFR, risk for delayed graft function (DGF), acute rejection and graft failure between the recipients of the two groups [135]

  • Regardless donor type, IRI is an unavoidable consequence after kidney transplantation that could lead to graft failure

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Summary

INTRODUCTION

Kidney transplantation represents the best treatment for patient with End-Stage Kidney Disease (ESKD) [1]. The trial, called EMPIRIKAL, aims to evaluate the efficacy of Mirococept in reducing the incidence of DGF in renal transplants from deceased donors [74, 75] and provided evidences on safety and feasibility of this new drug These preliminary data warrant further validation, these observations suggest that complement-targeted regulation before, during and after organ retrieval could modulate aberrant inflammation, regulating the IRI cytokine storm limiting renal damage and improving the outcome of transplantation. In a recent retrospective study, including 214 consecutive recipients from 122 brain-dead donors, meeting optimal donor management goals (DMGs) at donor neurological death is associated with a lower risk for DGF, independent of the use of machine perfusion and donor quality [129] In this scenario, donor pre-treatments have been investigated in several experimental and clinical studies with the goal of prevention and early treatment of organ injury during IRI, while only few studies analyzed their impact on graft survival [130]. Remote ischemic preconditioning (RIPC) has been used as a strategy to reduce acute kidney injury in the setting of cardiac surgery; while promising data suggested a Frontiers in Immunology | www.frontiersin.org

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CONCLUSION AND FUTURE PERSPECTIVES
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