Tacrolimus Trough Concentrations are Not Impacted by Epstein-Barr Virus Serology and Viral Load in Pediatric Liver Transplant Recipients
- PMID: 40528069
- DOI: 10.1007/s13318-025-00954-3
Tacrolimus Trough Concentrations are Not Impacted by Epstein-Barr Virus Serology and Viral Load in Pediatric Liver Transplant Recipients
Abstract
Background and objectives: Epstein-Barr virus (EBV) is a common herpesvirus among pediatric liver transplant recipients, but it can have serious complications, such as post-transplant lymphoproliferative disease. EBV is hypothesized to influence tacrolimus concentrations by increasing inflammatory cytokines that regulate the expression of cytochrome-P-450 enzymes involved in tacrolimus pharmacokinetics. This study aims to examine the association between EBV serostatus and viral load, and tacrolimus trough concentrations corrected for the dose and recipient weight [weight-adjusted concentration-to-dose (C/D) ratios].
Materials and methods: This retrospective study includes pediatric liver transplant recipients aged 0-18 years old, transplanted at the University Medical Center Groningen between January 2008 and September 2021. This study utilized two cohorts: a cross-sectional and a longitudinal study database.
Results: The association between EBV serostatus and the tacrolimus pharmacokinetics was examined using 45 recipients from both cohorts. The effect of EBV viral load on tacrolimus pharmacokinetics was examined using the longitudinal study database, which included 25 EBV-positive recipients. No significant effect of EBV on the tacrolimus weight-adjusted C/D ratios was found, for either EBV serostatus (p = 0.85) or EBV viral load (p = 0.85).
Conclusions: This study suggests that the standard protocol of tacrolimus dosing does not seem to require adjustments due to changes in EBV serostatus or viral load.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Conflict of Interest: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. Ethics Approval: This is a retrospective and descriptive study. The Medical Ethics Review Board of the University Medical Center Groningen (METc UMCG) has confirmed that this study does not fall under the scope of the Medical Research Involving Human Subjects Act (WMO), and therefore, no WMO required (METc 2019/621). Consent to Participate: Due to the retrospective and descriptive nature of this study, the need for informed consent was waived by the UMCG METc (METc 2019/621). Consent for Publication: No identifiable personal data is included in this study; therefore, consent for publication was not required. Code Availability: The data used in this study is owned by the UMCG and is not publicly available. No custom code was developed for this study. Authors’ Contribution Statements: Amber M. B. te Lintelo and Lisa F. van Wier contributed equally to this work. They were responsible for literature research, data extraction, data analysis, and writing the initial draft of the manuscript. Paola Mian, Daan J. Touw, and Hubert P. J. van der Doef contributed to the conceptualization of the study, data analysis, and writing and reviewing the manuscript. Coretta C. van Leer, René Scheenstra, Arno R. Bourgonje, and Jos. G. W. Kosterink contributed to reviewing the manuscript. All authors approved the final version of the manuscript.
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References
-
- Spada M, Riva S, Maggiore G, Cintorino D, Gridelli B. Pediatric liver transplantation. World J Gastroenterol: WJG. 2009;15(6):648. https://doi.org/10.3748/WJG.15.648 . - DOI - PubMed - PMC
-
- Mogul DB, Luo X, Bowring MG, et al. Fifteen-year trends in pediatric liver transplants: split, whole deceased, and living donor grafts. J Pediatr. 2018;196:148-153.e2. https://doi.org/10.1016/J.JPEDS.2017.11.015 . - DOI - PubMed - PMC
-
- Cuenca AG, Kim HB, Vakili K. Pediatric liver transplantation. Semin Pediatr Surg. 2017;26(4):217–23. https://doi.org/10.1053/J.SEMPEDSURG.2017.07.014 . - DOI - PubMed
-
- Dufour JF, Fey MF. What is the current treatment of PTLD after liver transplantation? J Hepatol. 2006;44(1):23–6. https://doi.org/10.1016/j.jhep.2005.10.009 . - DOI - PubMed
-
- Wiesner RH, Fung JJ. Present state of immunosuppressive therapy in liver transplant recipients. Liver Transpl. 2011;17(S3):S1–9. https://doi.org/10.1002/lt.22410 . - DOI - PubMed
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