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An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms

Current pre-transplantation routine matching involves serum anti-HLA antibodies quantification but cannot always preclude unfavorable graft outcomes. Epitope-based matching is proposed as a more precise approach, but to date no epitope-matching algorithm provides a satisfactory predictive tool for t...

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Autores principales: Fylaktou, Asimina, Lioulios, Georgios, Tarassi, Katerina, Siorenta, Alexandra, Petasis, George Ch, Gerogiannis, Demetris, Theodorou, Ioannis, Iniotaki, Aliki G., Vittoraki, Angeliki G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738260/
https://www.ncbi.nlm.nih.gov/pubmed/36498621
http://dx.doi.org/10.3390/jcm11237046
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author Fylaktou, Asimina
Lioulios, Georgios
Tarassi, Katerina
Siorenta, Alexandra
Petasis, George Ch
Gerogiannis, Demetris
Theodorou, Ioannis
Iniotaki, Aliki G.
Vittoraki, Angeliki G.
author_facet Fylaktou, Asimina
Lioulios, Georgios
Tarassi, Katerina
Siorenta, Alexandra
Petasis, George Ch
Gerogiannis, Demetris
Theodorou, Ioannis
Iniotaki, Aliki G.
Vittoraki, Angeliki G.
author_sort Fylaktou, Asimina
collection PubMed
description Current pre-transplantation routine matching involves serum anti-HLA antibodies quantification but cannot always preclude unfavorable graft outcomes. Epitope-based matching is proposed as a more precise approach, but to date no epitope-matching algorithm provides a satisfactory predictive tool for transplantation outcomes. In this study, anti-HLA-II loci responses from 1748 patients were analyzed with unsupervised machine learning algorithms, namely principal component analysis (PCA) and antigenic distances, projected as dendrograms. PCA for anti-HLA-DR anti-bodies revealed three main clusters of responses: anti-HLA-DR51 combined with anti-HLA-DRB1*01, anti-HLA-DR52 combined with anti-HLA-DRB1*08 and anti-HLA-DR53 combined with anti-HLA-DRB1*10. The dendrogram for anti-HLA-DR confirmed the pattern and showed further bisection of each cluster. Common epitopes present exclusively in all HLA molecules of each cluster were determined following the HLA epitope registry. Thus, we propose that 19 out of 123 HLA-DR epitopes are those that mainly lead anti-HLA-DR responses in the studied population. Likewise, we identified 22 out of 83 epitopes responsible for anti-HLA-DQ and 13 out of 62 responsible for anti-HLA-DP responses. Interpretation of these results may elucidate mechanisms of interlocus cross-reactivity, providing an alternative way of estimating the significance of each epitope in a population and thus suggesting a novel strategy towards optimal donor selection.
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spelling pubmed-97382602022-12-11 An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms Fylaktou, Asimina Lioulios, Georgios Tarassi, Katerina Siorenta, Alexandra Petasis, George Ch Gerogiannis, Demetris Theodorou, Ioannis Iniotaki, Aliki G. Vittoraki, Angeliki G. J Clin Med Article Current pre-transplantation routine matching involves serum anti-HLA antibodies quantification but cannot always preclude unfavorable graft outcomes. Epitope-based matching is proposed as a more precise approach, but to date no epitope-matching algorithm provides a satisfactory predictive tool for transplantation outcomes. In this study, anti-HLA-II loci responses from 1748 patients were analyzed with unsupervised machine learning algorithms, namely principal component analysis (PCA) and antigenic distances, projected as dendrograms. PCA for anti-HLA-DR anti-bodies revealed three main clusters of responses: anti-HLA-DR51 combined with anti-HLA-DRB1*01, anti-HLA-DR52 combined with anti-HLA-DRB1*08 and anti-HLA-DR53 combined with anti-HLA-DRB1*10. The dendrogram for anti-HLA-DR confirmed the pattern and showed further bisection of each cluster. Common epitopes present exclusively in all HLA molecules of each cluster were determined following the HLA epitope registry. Thus, we propose that 19 out of 123 HLA-DR epitopes are those that mainly lead anti-HLA-DR responses in the studied population. Likewise, we identified 22 out of 83 epitopes responsible for anti-HLA-DQ and 13 out of 62 responsible for anti-HLA-DP responses. Interpretation of these results may elucidate mechanisms of interlocus cross-reactivity, providing an alternative way of estimating the significance of each epitope in a population and thus suggesting a novel strategy towards optimal donor selection. MDPI 2022-11-29 /pmc/articles/PMC9738260/ /pubmed/36498621 http://dx.doi.org/10.3390/jcm11237046 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fylaktou, Asimina
Lioulios, Georgios
Tarassi, Katerina
Siorenta, Alexandra
Petasis, George Ch
Gerogiannis, Demetris
Theodorou, Ioannis
Iniotaki, Aliki G.
Vittoraki, Angeliki G.
An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms
title An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms
title_full An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms
title_fullStr An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms
title_full_unstemmed An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms
title_short An Approach to Identify HLA Class II Immunogenic Epitopes in the Greek Population through Machine Learning Algorithms
title_sort approach to identify hla class ii immunogenic epitopes in the greek population through machine learning algorithms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738260/
https://www.ncbi.nlm.nih.gov/pubmed/36498621
http://dx.doi.org/10.3390/jcm11237046
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