Evidence map›Paper›PMID 42877279›Full record

ArticleFrontiers in pharmacology2026

Dynamic kinetics of graft-derived cell-free DNA and personalized tacrolimus target ranges for acute rejection monitoring in pediatric liver transplantation.

Meiling Yan, Jia Zhao, Wei Gao, Yinpeng Qin, Jun Lu, Yi Zhang

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Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Meiling YanDepartment of Science and Education, Tianjin First Central Hospital, Tianjin, China.
Jia ZhaoDepartment of Pharmacy, Tianjin Chest Hospital, Tianjin, China.
Wei GaoDepartment of Liver Transplantation, Organ Transplantation Center, Tianjin First Central Hospital, Tianjin, China.
Yinpeng QinDepartment of Science and Education, Tianjin First Central Hospital, Tianjin, China.
Jun LuS&KM Biotechnology Co., Ltd., Chengdu, Sichuan, China.
Yi ZhangDepartment of Science and Education, Tianjin First Central Hospital, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Acute rejection remains the most common complication during the early post-transplantation period for pediatric patients. Given the limitations of current diagnostic strategies, there is an urgent need to develop accurate and noninvasive biomarkers for allograft monitoring. Tacrolimus-based immunosuppression represents the cornerstone regimen following liver transplantation. However, for pediatric patients, current evidence remains insufficient to establish well-defined therapeutic target ranges for personalized tacrolimus therapy in pediatric patients. We investigated perioperative graft-derived cell-free DNA (GcfDNA) kinetics in pediatric recipients to establish the utility of GcfDNA for monitoring acute rejection and to explore the tacrolimus target concentration range in this population. Methods: Forty children (age ≤ 3 years) with biliary atresia who underwent liver transplantation were enrolled. All received a tacrolimus-based immunosuppressive regimen on postoperative day (POD) 1 and were followed for at least 1 month. GcfDNA levels were measured by droplet digital PCR. Results: GcfDNA (%) declined significantly during the first month. Median percentages on POD 1, 7, 14, 21, and 28 were 41.40%, 12.93%, 6.86%, 5.95%, and 3.23%, respectively. The acute rejection group maintained higher GcfDNA levels, with significant differences observed at POD 14, 21, and 28 ( Conclusion: We suggest that GcfDNA may serve as a potential biomarker for acute rejection monitoring in pediatric liver transplantation, with an exploratory predictive cutoff value of 10.21% identified in this single-center cohort. Our findings also tentatively point to a minimal effective tacrolimus C

Indexed as

acute rejectiongraft-derived cell-free DNAmonitoringpediatric liver transplantationtacrolimus trough concentration

Identifiers

PMID42877279
PMCPMC13662168

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