Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsis

Highly heterogeneous cell populations require multiple flow cytometric markers for appropriate phenotypic characterization. This exponentially increases the complexity of 2D scatter plot analyses and exacerbates human errors due to variations in manual gating of flow data. We describe a semi-automat...

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Main Authors: Anthony S. Bonavia, Abigail Samuelsen, Joshua Luthy, E. Scott Halstead
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-11-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.1007016/full
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author Anthony S. Bonavia
Anthony S. Bonavia
Abigail Samuelsen
Joshua Luthy
E. Scott Halstead
author_facet Anthony S. Bonavia
Anthony S. Bonavia
Abigail Samuelsen
Joshua Luthy
E. Scott Halstead
author_sort Anthony S. Bonavia
collection DOAJ
description Highly heterogeneous cell populations require multiple flow cytometric markers for appropriate phenotypic characterization. This exponentially increases the complexity of 2D scatter plot analyses and exacerbates human errors due to variations in manual gating of flow data. We describe a semi-automated workflow, based entirely on the Flowjo Graphical User Interface (GUI), that involves the stepwise integration of several, newly available machine learning tools for the analysis of myeloid-derived suppressor cells (MDSCs) in septic and non-septic critical illness. Supervised clustering of flow cytometric data showed correlation with, but significantly different numbers of, MDSCs as compared with the cell numbers obtained by manual gating. Neither quantification method predicted 30-day clinical outcomes in a cohort of 16 critically ill and septic patients and 5 critically ill and non-septic patients. Machine learning identified a significant decrease in the proportion of PMN-MDSC in critically ill and septic patients as compared with healthy controls. There was no difference between the proportion of these MDSCs in septic and non-septic critical illness.
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spelling doaj.art-263bece57cb74cbeb38ef89a98bf31532022-12-22T04:14:47ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-11-011310.3389/fimmu.2022.10070161007016Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsisAnthony S. Bonavia0Anthony S. Bonavia1Abigail Samuelsen2Joshua Luthy3E. Scott Halstead4Division of Critical Care Medicine, Department of Anesthesiology and Perioperative Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA, United StatesDepartment of Anesthesiology and Perioperative Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA, United StatesDivision of Critical Care Medicine, Department of Anesthesiology and Perioperative Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA, United StatesProduct Innovation Division, BD Life Sciences - FlowJo, Ashland, OR, United StatesDivision of Pediatric Critical Care Medicine, Department of Pediatrics, Penn State Milton S. Hershey Medical Center, Hershey, PA, United StatesHighly heterogeneous cell populations require multiple flow cytometric markers for appropriate phenotypic characterization. This exponentially increases the complexity of 2D scatter plot analyses and exacerbates human errors due to variations in manual gating of flow data. We describe a semi-automated workflow, based entirely on the Flowjo Graphical User Interface (GUI), that involves the stepwise integration of several, newly available machine learning tools for the analysis of myeloid-derived suppressor cells (MDSCs) in septic and non-septic critical illness. Supervised clustering of flow cytometric data showed correlation with, but significantly different numbers of, MDSCs as compared with the cell numbers obtained by manual gating. Neither quantification method predicted 30-day clinical outcomes in a cohort of 16 critically ill and septic patients and 5 critically ill and non-septic patients. Machine learning identified a significant decrease in the proportion of PMN-MDSC in critically ill and septic patients as compared with healthy controls. There was no difference between the proportion of these MDSCs in septic and non-septic critical illness.https://www.frontiersin.org/articles/10.3389/fimmu.2022.1007016/fullhigh parameter flow cytometrysepsis - diagnosticsclustering analysisclinical immunologymyeloid-derived suppressor cells (MDSC)
spellingShingle Anthony S. Bonavia
Anthony S. Bonavia
Abigail Samuelsen
Joshua Luthy
E. Scott Halstead
Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsis
Frontiers in Immunology
high parameter flow cytometry
sepsis - diagnostics
clustering analysis
clinical immunology
myeloid-derived suppressor cells (MDSC)
title Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsis
title_full Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsis
title_fullStr Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsis
title_full_unstemmed Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsis
title_short Integrated machine learning approaches for flow cytometric quantification of myeloid-derived suppressor cells in acute sepsis
title_sort integrated machine learning approaches for flow cytometric quantification of myeloid derived suppressor cells in acute sepsis
topic high parameter flow cytometry
sepsis - diagnostics
clustering analysis
clinical immunology
myeloid-derived suppressor cells (MDSC)
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.1007016/full
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