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Introduction: During the coronavirus disease 2019 (Covid-19) pandemic, several physicians have questioned pursuing belatacept in kidney-transplant patients in order to reduce the risk of nosocomial transmission during the monthly infusion. The effect of the conversion from belatacept to another immunosuppressive regimen is underreported. The aim of the present retrospective study was to assess the effect on kidney function and the clinical outcome of the conversion from belatacept to another regimen.
Methods: We have identified 44 maintenance kidney transplantation patients from five French kidney transplantation centers who were converted from belatacept to another regimen either because of a complication (n = 28) or another reason (patients' request or belatacept shortage, n = 13). The follow-up after the conversion from belatacept was 27.5 ± 25.3 months.
Results: Overall, mean estimated glomerular filtration rate (eGFR) decreased from 44.2 ± 16 ml/min per 1.73 m at conversion from belatacept to 35.7 ± 18.4 ml/min per 1.73 m at last follow-up ( = 0.0002). eGFR significantly decreased in patients who had been given belatacept at transplantation as well as in those who had been converted to belatacept earlier. The decrease was less significant in patients who had stopped belatacept without having experienced any complications. Finally, eGFR decreased more severely in patients who were converted to calcineurin inhibitors (CNIs), compared to those who received mammalian target of rapamycin inhibitor (mTORi). Few patients also developed diabetes and hypertension.
Conclusions: Thus, transplantation physicians should avoid stopping belatacept when not clinically required.
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http://dx.doi.org/10.1016/j.ekir.2020.09.036 | DOI Listing |
Transplantation
September 2025
Department of Nephrology, Hemodialysis, Apheresis and Kidney Transplantation, Centre Hospitalier Universitaire Grenoble-Alpes, University Grenoble Alpes, Grenoble, France.
Although maintenance immunosuppression with calcineurin inhibitors (CNIs) has greatly reduced rejection rates in renal transplant recipients, long-term use can contribute to eventual nephrotoxicity, potentially leading to allograft injury and loss. Several clinical trials have shown that, compared with CNIs, belatacept-based maintenance immunosuppression can improve renal function, reduce the incidence of de novo donor-specific antibodies, and improve long-term patient/graft survival. However, the US Food and Drug Administration-approved belatacept-based regimen is also associated with higher acute rejection (AR) rates than CNI-based immunosuppression.
View Article and Find Full Text PDFClin Transplant
July 2025
Nephrology Associates of Utah, Salt Lake City, Utah, USA.
Belatacept (Bt) conversion is associated with increased rejection risk in kidney transplant patients (KTxP). The study included patients who underwent kidney transplant and were converted to Bt. Induction was given, followed by maintenance with a calcineurin inhibitor (CNI), antimetabolite, and steroid.
View Article and Find Full Text PDFKidney Int Rep
June 2025
Pediatric Nephrology Department, Emory School of Medicine and Children's Healthcare of Atlanta, Georgia, USA.
Introduction: Belatacept (CTLA4-Ig) has shown efficacy in adult kidney transplantation (KT) recipients (improved graft and patient survival and reduced donor-specific antibody [DSA]) compared with calcineurin inhibitors (CNIs). Its long-term benefits and monthly i.v.
View Article and Find Full Text PDFKidney Int Rep
June 2025
Nephrology, Dialysis and Kidney Transplantation Department, Rouen University Hospital, Rouen, France.
Transpl Int
June 2025
Department of Nephrology, Transplantation and Hemodialysis, Rouen University Hospital, Rouen, France.
Calcineurin inhibitors (CNIs) are a cornerstone of post-transplant immunosuppressive regimens. However, their use is associated with adverse effects, most notably chronic nephrotoxicity, which remains a leading cause of long-term allograft dysfunction. Belatacept, a selective costimulation blocker, offers a promising alternative to CNIs by aiming to reduce nephrotoxicity while maintaining efficacy in preventing acute rejection.
View Article and Find Full Text PDF