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Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms
Allele specific antibody response against the polymorphic system of HLA is the allogeneic response marker determining the immunological risk for graft acceptance before and after organ transplantation and therefore routinely studied during the patient's workup. Experimentally, bead bound antige...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399170/ https://www.ncbi.nlm.nih.gov/pubmed/32849576 http://dx.doi.org/10.3389/fimmu.2020.01667 |
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author | Vittoraki, Angeliki G. Fylaktou, Asimina Tarassi, Katerina Tsinaris, Zafeiris Petasis, George Ch. Gerogiannis, Demetris Kheav, Vissal-David Carmagnat, Maryvonnick Lehmann, Claudia Doxiadis, Ilias Iniotaki, Aliki G. Theodorou, Ioannis |
author_facet | Vittoraki, Angeliki G. Fylaktou, Asimina Tarassi, Katerina Tsinaris, Zafeiris Petasis, George Ch. Gerogiannis, Demetris Kheav, Vissal-David Carmagnat, Maryvonnick Lehmann, Claudia Doxiadis, Ilias Iniotaki, Aliki G. Theodorou, Ioannis |
author_sort | Vittoraki, Angeliki G. |
collection | PubMed |
description | Allele specific antibody response against the polymorphic system of HLA is the allogeneic response marker determining the immunological risk for graft acceptance before and after organ transplantation and therefore routinely studied during the patient's workup. Experimentally, bead bound antigen- antibody reactions are detected using a special multicolor flow cytometer (Luminex). Routinely for each sample, antibody responses against 96 different HLA antigen groups are measured simultaneously and a 96-dimensional immune response vector is created. Under a common experimental protocol, using unsupervised clustering algorithms, we analyzed these immune intensity vectors of anti HLA class II responses from a dataset of 1,748 patients before or after renal transplantation residing in a single country. Each patient contributes only one serum sample in the analysis. A population view of linear correlations of hierarchically ordered fluorescence intensities reveals patterns in human immune responses with striking similarities with the previously described CREGs but also brings new information on the antigenic properties of class II HLA molecules. The same analysis affirms that “public” anti-DP antigenic responses are not correlated to anti DR and anti DQ responses which tend to cluster together. Principal Component Analysis (PCA) projections also demonstrate ordering patterns clearly differentiating anti DP responses from anti DR and DQ on several orthogonal planes. We conclude that a computer vision of human alloresponse by use of several dimensionality reduction algorithms rediscovers proven patterns of immune reactivity without any a priori assumption and might prove helpful for a more accurate definition of public immunogenic antigenic structures of HLA molecules. Furthermore, the use of Eigen decomposition on the Immune Response generates new hypotheses that may guide the design of more effective patient monitoring tests. |
format | Online Article Text |
id | pubmed-7399170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73991702020-08-25 Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms Vittoraki, Angeliki G. Fylaktou, Asimina Tarassi, Katerina Tsinaris, Zafeiris Petasis, George Ch. Gerogiannis, Demetris Kheav, Vissal-David Carmagnat, Maryvonnick Lehmann, Claudia Doxiadis, Ilias Iniotaki, Aliki G. Theodorou, Ioannis Front Immunol Immunology Allele specific antibody response against the polymorphic system of HLA is the allogeneic response marker determining the immunological risk for graft acceptance before and after organ transplantation and therefore routinely studied during the patient's workup. Experimentally, bead bound antigen- antibody reactions are detected using a special multicolor flow cytometer (Luminex). Routinely for each sample, antibody responses against 96 different HLA antigen groups are measured simultaneously and a 96-dimensional immune response vector is created. Under a common experimental protocol, using unsupervised clustering algorithms, we analyzed these immune intensity vectors of anti HLA class II responses from a dataset of 1,748 patients before or after renal transplantation residing in a single country. Each patient contributes only one serum sample in the analysis. A population view of linear correlations of hierarchically ordered fluorescence intensities reveals patterns in human immune responses with striking similarities with the previously described CREGs but also brings new information on the antigenic properties of class II HLA molecules. The same analysis affirms that “public” anti-DP antigenic responses are not correlated to anti DR and anti DQ responses which tend to cluster together. Principal Component Analysis (PCA) projections also demonstrate ordering patterns clearly differentiating anti DP responses from anti DR and DQ on several orthogonal planes. We conclude that a computer vision of human alloresponse by use of several dimensionality reduction algorithms rediscovers proven patterns of immune reactivity without any a priori assumption and might prove helpful for a more accurate definition of public immunogenic antigenic structures of HLA molecules. Furthermore, the use of Eigen decomposition on the Immune Response generates new hypotheses that may guide the design of more effective patient monitoring tests. Frontiers Media S.A. 2020-07-28 /pmc/articles/PMC7399170/ /pubmed/32849576 http://dx.doi.org/10.3389/fimmu.2020.01667 Text en Copyright © 2020 Vittoraki, Fylaktou, Tarassi, Tsinaris, Petasis, Gerogiannis, Kheav, Carmagnat, Lehmann, Doxiadis, Iniotaki and Theodorou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Vittoraki, Angeliki G. Fylaktou, Asimina Tarassi, Katerina Tsinaris, Zafeiris Petasis, George Ch. Gerogiannis, Demetris Kheav, Vissal-David Carmagnat, Maryvonnick Lehmann, Claudia Doxiadis, Ilias Iniotaki, Aliki G. Theodorou, Ioannis Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms |
title | Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms |
title_full | Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms |
title_fullStr | Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms |
title_full_unstemmed | Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms |
title_short | Patterns of 1,748 Unique Human Alloimmune Responses Seen by Simple Machine Learning Algorithms |
title_sort | patterns of 1,748 unique human alloimmune responses seen by simple machine learning algorithms |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399170/ https://www.ncbi.nlm.nih.gov/pubmed/32849576 http://dx.doi.org/10.3389/fimmu.2020.01667 |
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