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In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
Comparable outcomes with anti-thymocyte globulins versus basiliximab in kidney transplantation from controlled
Martin Deslais1, Alice Koenig1,2, Fanny Buron1
1Department of Transplantation, Nephrology and Clinical Immunology, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.
Insights
Basiliximab is a cost-effective alternative to anti-thymocyte globulin (ATG) for kidney transplants using donation after circulatory death (DCD) grafts in low-risk patients. This study found similar graft outcomes and safety profiles between the two induction therapies.
Area of Science:
- Nephrology
- Transplantation Immunology
- Organ Donation
Background:
- Donation after circulatory death (DCD) kidney grafts are increasingly used due to organ shortages.
- DCD grafts have higher rates of delayed graft function (DGF), leading to specific management protocols.
- The French national protocol recommends hypothermic machine perfusion and anti-thymocyte globulin (ATG) for DCD kidney transplants.
Purpose of the Study:
- To compare the efficacy and safety of basiliximab versus ATG induction therapy in low immunological risk DCD kidney transplantation.
- To evaluate the cost-effectiveness of basiliximab as an alternative to ATG in this patient population.
Main Methods:
- Retrospective analysis of a single-center cohort (n=158) of low-risk DCD kidney transplant recipients (2015-2023).
- Comparison of outcomes between patients receiving ATG (pre-March 2020) and basiliximab (post-March 2020).
- Validation of findings in an independent French multicenter cohort (n=506).
Main Results:
- No significant differences in primary non-function, DGF rates (17% ATG vs. 12% basiliximab), rejection, one-year renal function, or graft survival.
- ATG was associated with prolonged Epstein-Barr virus (EBV) and BK viremia without increased complications.
- Basiliximab induction was associated with a 1.7-fold lower cost compared to ATG, with similar hospital stays.
Conclusions:
- Basiliximab is a viable and cost-effective alternative to ATG for low-immunological-risk DCD kidney transplant recipients.
- Current evidence does not strongly favor ATG over basiliximab for this specific patient group.
- This finding supports a potential shift in induction therapy protocols for DCD kidney transplantation.
Abstract:
Due to organ shortage, donation after circulatory death (DCD) has increased. As DCD kidney grafts have higher rates of delayed graft function (DGF), the French national protocol mandates the use of hypothermic machine perfusion and routine anti-thymocyte globulin (ATG) induction therapy. However, evidence favoring ATG over interleukin-2 receptor antagonists, such as basiliximab, remains scarce. We retrospectively analysed a single-center cohort of 158 low immunological risk patients who underwent DCD kidney transplantation between 2015 and 2023. Patients transplanted before March 2020 received ATG (n = 64), while those transplanted thereafter (during and after the COVID-19 pandemic) received basiliximab (n = 94). Baseline characteristics were comparable, except for recipient age (lower in the basiliximab group), and cold ischemia times were similar. There were no differences in primary non-function, DGF rates (17% after ATG versus 12% after basiliximab), biopsy-proven rejection, one-year renal function or graft survival. ATG was associated with prolonged EBV and BK viremia without increased complications. Hospital stays were similar, but ATG induction was 1.7 times more expensive. These findings were confirmed in an independent French multicenter cohort (n = 506). In conclusion, basiliximab appears to be a cost-effective alternative to ATG for low-immunological-risk patients receiving DCD kidney grafts, for whom ATG is not clearly indicated.
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