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The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models
BACKGROUND: Kidney transplantation is the optimal treatment to cure the patients with end-stage renal disease (ESRD). However, the infectious complication, especially pneumonia, is the main cause of mortality in the early stage. Immune monitoring by relevant biomarkers provides direct evidence of im...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526199/ https://www.ncbi.nlm.nih.gov/pubmed/32993687 http://dx.doi.org/10.1186/s12967-020-02542-2 |
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author | Peng, Bo Gong, Hang Tian, Han Zhuang, Quan Li, Junhui Cheng, Ke Ming, Yingzi |
author_facet | Peng, Bo Gong, Hang Tian, Han Zhuang, Quan Li, Junhui Cheng, Ke Ming, Yingzi |
author_sort | Peng, Bo |
collection | PubMed |
description | BACKGROUND: Kidney transplantation is the optimal treatment to cure the patients with end-stage renal disease (ESRD). However, the infectious complication, especially pneumonia, is the main cause of mortality in the early stage. Immune monitoring by relevant biomarkers provides direct evidence of immune status. We aimed to study the association between immune monitoring and pneumonia in kidney transplant patients through machine learning models. METHODS: A total of 146 patients receiving the immune monitoring panel in our center, including 46 pneumonia recipients and 100 stable recipients, were retrospectively reviewed to develop the models. All the models were validated by external data containing 10 pneumonia recipients and 32 stable recipients. The immune monitoring panel consisted of the percentages and absolute cell counts of CD3(+)CD4(+) T cells, CD3(+)CD8(+) T cells, CD19(+) B cells and natural killer (NK) cells, and median fluorescence intensity (MFI) of human leukocyte antigen (HLA)-DR on monocytes and CD64 on neutrophils. The machine learning models including support vector machine (SVM), logistic regression (LR), multi-layer perceptron (MLP) and random forest (RF) were applied for analysis. RESULTS: The pneumonia and stable groups showed significant difference in cell counts of each subpopulation and MFI of monocyte HLA-DR and neutrophil CD64. The SVM model by monocyte HLA-DR (MFI), neutrophil CD64 (MFI), CD8(+) T cells (cells/μl), NK cells (cell/μl) and TBNK (T cells, B cells and NK cells, cells/μl) had the best performance with the average area under the curve (AUC) of 0.940. The RF model best predicted the patients who would progress into severe pneumonia, with the average AUC of 0.760. All the models had good performance validated by external data. CONCLUSIONS: The immune monitoring panel was tightly associated with pneumonia in kidney transplant recipients. The models developed by machine learning techniques identified patients at risk and predicted the prognosis. Based on the results of immune monitoring, better individualized therapy might be achieved. |
format | Online Article Text |
id | pubmed-7526199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75261992020-09-30 The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models Peng, Bo Gong, Hang Tian, Han Zhuang, Quan Li, Junhui Cheng, Ke Ming, Yingzi J Transl Med Research BACKGROUND: Kidney transplantation is the optimal treatment to cure the patients with end-stage renal disease (ESRD). However, the infectious complication, especially pneumonia, is the main cause of mortality in the early stage. Immune monitoring by relevant biomarkers provides direct evidence of immune status. We aimed to study the association between immune monitoring and pneumonia in kidney transplant patients through machine learning models. METHODS: A total of 146 patients receiving the immune monitoring panel in our center, including 46 pneumonia recipients and 100 stable recipients, were retrospectively reviewed to develop the models. All the models were validated by external data containing 10 pneumonia recipients and 32 stable recipients. The immune monitoring panel consisted of the percentages and absolute cell counts of CD3(+)CD4(+) T cells, CD3(+)CD8(+) T cells, CD19(+) B cells and natural killer (NK) cells, and median fluorescence intensity (MFI) of human leukocyte antigen (HLA)-DR on monocytes and CD64 on neutrophils. The machine learning models including support vector machine (SVM), logistic regression (LR), multi-layer perceptron (MLP) and random forest (RF) were applied for analysis. RESULTS: The pneumonia and stable groups showed significant difference in cell counts of each subpopulation and MFI of monocyte HLA-DR and neutrophil CD64. The SVM model by monocyte HLA-DR (MFI), neutrophil CD64 (MFI), CD8(+) T cells (cells/μl), NK cells (cell/μl) and TBNK (T cells, B cells and NK cells, cells/μl) had the best performance with the average area under the curve (AUC) of 0.940. The RF model best predicted the patients who would progress into severe pneumonia, with the average AUC of 0.760. All the models had good performance validated by external data. CONCLUSIONS: The immune monitoring panel was tightly associated with pneumonia in kidney transplant recipients. The models developed by machine learning techniques identified patients at risk and predicted the prognosis. Based on the results of immune monitoring, better individualized therapy might be achieved. BioMed Central 2020-09-29 /pmc/articles/PMC7526199/ /pubmed/32993687 http://dx.doi.org/10.1186/s12967-020-02542-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Peng, Bo Gong, Hang Tian, Han Zhuang, Quan Li, Junhui Cheng, Ke Ming, Yingzi The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models |
title | The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models |
title_full | The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models |
title_fullStr | The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models |
title_full_unstemmed | The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models |
title_short | The study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models |
title_sort | study of the association between immune monitoring and pneumonia in kidney transplant recipients through machine learning models |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526199/ https://www.ncbi.nlm.nih.gov/pubmed/32993687 http://dx.doi.org/10.1186/s12967-020-02542-2 |
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