4.6 Article

CMV high-risk status and posttransplant outcomes in kidney transplant recipients treated with belatacept

期刊

AMERICAN JOURNAL OF TRANSPLANTATION
卷 21, 期 1, 页码 208-221

出版社

WILEY
DOI: 10.1111/ajt.16132

关键词

clinical research; practice; complication; infectious; immunosuppressant - fusion proteins and monoclonal antibodies; belatacept; immunosuppression; immune modulation; immunosuppressive regimens - maintenance; infection and infectious agents - viral; Cytomegalovirus (CMV); infectious disease; kidney (allograft) function; dysfunction; kidney transplantation; nephrology; translational research; science

资金

  1. James M. Cox Foundation
  2. Carlos and Marguerite Mason Trust

向作者/读者索取更多资源

In CMV high-risk kidney transplant recipients, belatacept-based maintenance immunosuppression may increase the risk of primary CMV infection and prolong the course of viral replication. While patients treated with belatacept showed a trend towards lower graft survival, this conclusion was not statistically significant. Further studies are needed to confirm these findings and explore the relationship between belatacept treatment and CMV outcomes.
Introduction Cytomegalovirus (CMV) remains associated with poor outcomes after kidney transplantation (kTx). The impact of belatacept on CMV infection remains understudied. In this study, we assessed the impact of belatacept on patient and graft survivals. Methods CMV seronegative kTx recipients were included. Patient and graft survival were studied using Kaplan-Meier method, log-rank test. Cox models were used to compare outcomes by CMV risk and immunosuppressive regimen. Incidence and persistence of CMV viremia under belatacept vs tacrolimus were compared. Results Among 308 CMV seronegative recipients, 168 CMV high-risk and 203 belatacept-treated patients were included. High-risk CMV status was associated with lower patient survival and graft survival. Among the CMV high-risk group, patients treated with belatacept presented a higher incidence of CMV viremia, a higher rate of first-line treatment failure and a longer time to virus clearance. They had a nonsignificant trend toward a lower graft survival. Conclusion Belatacept-based maintenance immunosuppression is associated with an increased risk of CMV primary-infection and a prolonged course of viral replication in CMV high-risk patients. Further studies are needed to confirm the nonsignificant trend towards a lower graft survival in CMV high-risk patients treated with belatacept and whether it is explained by the higher risk of CMV reactivation and infection.

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