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

HLAMatchmaker PIRCHE II epitope graft kidney mismatch pediatric renal transplantation

Journal

Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936

Informations de publication

Date de publication:
30 Oct 2023
Historique:
received: 07 09 2023
revised: 20 09 2023
accepted: 25 10 2023
medline: 25 11 2023
pubmed: 25 11 2023
entrez: 25 11 2023
Statut: epublish

Résumé

(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.

Identifiants

pubmed: 38002848
pii: children10111756
doi: 10.3390/children10111756
pmc: PMC10670802
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Paul Luchian Aldea (PL)

Clinical Institute of Urology and Renal Transplantation, 400006 Cluj-Napoca, Romania.

Maria Diana Santionean (MD)

Department of Mother and Child, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.

Alina Elec (A)

Clinical Institute of Urology and Renal Transplantation, 400006 Cluj-Napoca, Romania.

Adriana Munteanu (A)

Clinical Institute of Urology and Renal Transplantation, 400006 Cluj-Napoca, Romania.

Oana Antal (O)

Clinical Institute of Urology and Renal Transplantation, 400006 Cluj-Napoca, Romania.
Department of Urology, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.

Luminita Loga (L)

Clinical Institute of Urology and Renal Transplantation, 400006 Cluj-Napoca, Romania.

Tudor Moisoiu (T)

Clinical Institute of Urology and Renal Transplantation, 400006 Cluj-Napoca, Romania.
Department of Urology, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.

Florin Ioan Elec (FI)

Clinical Institute of Urology and Renal Transplantation, 400006 Cluj-Napoca, Romania.
Department of Urology, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.

Dan Delean (D)

Department of Mother and Child, Discipline of Pediatrics II, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.

Bogdan Bulata (B)

Department of Mother and Child, Discipline of Pediatrics II, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.

Andreea Liana Rachisan Bot (AL)

Department of Mother and Child, Discipline of Pediatrics II, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.

Classifications MeSH