An Integrated Approach Using HLAMatchmaker and Pirche II for Epitopic Matching in Pediatric Kidney Transplant-A Romanian Single-Center Study

被引:3
作者
Aldea, Paul Luchian [1 ]
Santionean, Maria Diana [2 ]
Elec, Alina [1 ]
Munteanu, Adriana [1 ]
Antal, Oana [1 ,3 ]
Loga, Luminita [1 ]
Moisoiu, Tudor [1 ,3 ]
Elec, Florin Ioan [1 ,3 ]
Delean, Dan [4 ]
Bulata, Bogdan [4 ]
Rachisan , Andreea Liana [4 ]
机构
[1] Clin Inst Urol & Renal Transplantat, Cluj Napoca 400006, Romania
[2] Iuliu Hatieganu Univ Med & Pharm, Dept Mother & Child, Cluj Napoca 400347, Romania
[3] Iuliu Hatieganu Univ Med & Pharm, Dept Urol, Cluj Napoca 400347, Romania
[4] Iuliu Hatieganu Univ Med & Pharm, Dept Mother & Child, Discipline Pediat 2, Cluj Napoca 400347, Romania
来源
CHILDREN-BASEL | 2023年 / 10卷 / 11期
关键词
kidney; transplantation; epitope; pediatric; renal; graft; HLAMatchmaker; PIRCHE II; mismatch; HLA EPITOPES; EPLET MISMATCHES; ANTIBODIES; CORRELATE;
D O I
10.3390/children10111756
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
(1) Background: Renal transplantation (KT) is the most efficient treatment for chronic kidney disease among pediatric patients. Antigenic matching and epitopic load should be the main criteria for choosing a renal graft in pediatric transplantation. Our study aims to compare the integration of new histocompatibility predictive algorithms with classical human leukocyte antigen (HLA) matching regarding different types of pediatric renal transplants. (2) Methods: We categorized our cohort of pediatric patients depending on their risk level, type of donor and type of transplantation, delving into discussions surrounding their mismatching values in relation to both the human leukocyte antigen Matchmaker software (versions 4.0. and 3.1.) and the most recent version of the predicted indirectly identifiable HLA epitopes (PIRCHE) II score. (3) Results: We determined that the higher the antigen mismatch, the higher the epitopic load for both algorithms. The HLAMatchmaker algorithm reveals a noticeable difference in eplet load between living and deceased donors, whereas PIRCHE II does not show the same distinction. Dialysis recipients have a higher count of eplet mismatches, which demonstrates a significant difference according to the transplantation type. Our results are similar to those of four similar studies available in the current literature. (4) Conclusions: We suggest that an integrated data approach employing PIRCHE II and HLAMatchmaker algorithms better predicts histocompatibility in KT than classical HLA matching.
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页数:11
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