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A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls

Cytokines and chemokines are key signaling molecules of the immune system. Recent technological advances enable measurement of multiplexed cytokine profiles in biological samples. These profiles can then be used to identify potential biomarkers of a variety of clinical phenotypes. However, testing f...

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Autores principales: Cohen, Liel, Fiore-Gartland, Andrew, Randolph, Adrienne G., Panoskaltsis-Mortari, Angela, Wong, Sook-San, Ralston, Jacqui, Wood, Timothy, Seeds, Ruth, Huang, Q. Sue, Webby, Richard J., Thomas, Paul G., Hertz, Tomer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594355/
https://www.ncbi.nlm.nih.gov/pubmed/31275311
http://dx.doi.org/10.3389/fimmu.2019.01338
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author Cohen, Liel
Fiore-Gartland, Andrew
Randolph, Adrienne G.
Panoskaltsis-Mortari, Angela
Wong, Sook-San
Ralston, Jacqui
Wood, Timothy
Seeds, Ruth
Huang, Q. Sue
Webby, Richard J.
Thomas, Paul G.
Hertz, Tomer
author_facet Cohen, Liel
Fiore-Gartland, Andrew
Randolph, Adrienne G.
Panoskaltsis-Mortari, Angela
Wong, Sook-San
Ralston, Jacqui
Wood, Timothy
Seeds, Ruth
Huang, Q. Sue
Webby, Richard J.
Thomas, Paul G.
Hertz, Tomer
author_sort Cohen, Liel
collection PubMed
description Cytokines and chemokines are key signaling molecules of the immune system. Recent technological advances enable measurement of multiplexed cytokine profiles in biological samples. These profiles can then be used to identify potential biomarkers of a variety of clinical phenotypes. However, testing for such associations for each cytokine separately ignores the highly context-dependent covariation in cytokine secretion and decreases statistical power to detect associations due to multiple hypothesis testing. Here we present CytoMod—a novel data-driven approach for analysis of cytokine profiles that uses unsupervised clustering and regression to identify putative functional modules of co-signaling cytokines. Each module represents a biosignature of co-signaling cytokines. We applied this approach to three independent clinical cohorts of subjects naturally infected with influenza in which cytokine profiles and clinical phenotypes were collected. We found that in two out of three cohorts, cytokine modules were significantly associated with clinical phenotypes, and in many cases these associations were stronger than the associations of the individual cytokines within them. By comparing cytokine modules across datasets, we identified cytokine “cores”—specific subsets of co-expressed cytokines that clustered together across the three cohorts. Cytokine cores were also associated with clinical phenotypes. Interestingly, most of these cores were also co-expressed in a cohort of healthy controls, suggesting that in part, patterns of cytokine co-signaling may be generalizable. CytoMod can be readily applied to any cytokine profile dataset regardless of measurement technology, increases the statistical power to detect associations with clinical phenotypes and may help shed light on the complex co-signaling networks of cytokines in both health and infection.
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spelling pubmed-65943552019-07-03 A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls Cohen, Liel Fiore-Gartland, Andrew Randolph, Adrienne G. Panoskaltsis-Mortari, Angela Wong, Sook-San Ralston, Jacqui Wood, Timothy Seeds, Ruth Huang, Q. Sue Webby, Richard J. Thomas, Paul G. Hertz, Tomer Front Immunol Immunology Cytokines and chemokines are key signaling molecules of the immune system. Recent technological advances enable measurement of multiplexed cytokine profiles in biological samples. These profiles can then be used to identify potential biomarkers of a variety of clinical phenotypes. However, testing for such associations for each cytokine separately ignores the highly context-dependent covariation in cytokine secretion and decreases statistical power to detect associations due to multiple hypothesis testing. Here we present CytoMod—a novel data-driven approach for analysis of cytokine profiles that uses unsupervised clustering and regression to identify putative functional modules of co-signaling cytokines. Each module represents a biosignature of co-signaling cytokines. We applied this approach to three independent clinical cohorts of subjects naturally infected with influenza in which cytokine profiles and clinical phenotypes were collected. We found that in two out of three cohorts, cytokine modules were significantly associated with clinical phenotypes, and in many cases these associations were stronger than the associations of the individual cytokines within them. By comparing cytokine modules across datasets, we identified cytokine “cores”—specific subsets of co-expressed cytokines that clustered together across the three cohorts. Cytokine cores were also associated with clinical phenotypes. Interestingly, most of these cores were also co-expressed in a cohort of healthy controls, suggesting that in part, patterns of cytokine co-signaling may be generalizable. CytoMod can be readily applied to any cytokine profile dataset regardless of measurement technology, increases the statistical power to detect associations with clinical phenotypes and may help shed light on the complex co-signaling networks of cytokines in both health and infection. Frontiers Media S.A. 2019-06-18 /pmc/articles/PMC6594355/ /pubmed/31275311 http://dx.doi.org/10.3389/fimmu.2019.01338 Text en Copyright © 2019 Cohen, Fiore-Gartland, Randolph, Panoskaltsis-Mortari, Wong, Ralston, Wood, Seeds, Huang, Webby, Thomas and Hertz. 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
Cohen, Liel
Fiore-Gartland, Andrew
Randolph, Adrienne G.
Panoskaltsis-Mortari, Angela
Wong, Sook-San
Ralston, Jacqui
Wood, Timothy
Seeds, Ruth
Huang, Q. Sue
Webby, Richard J.
Thomas, Paul G.
Hertz, Tomer
A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls
title A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls
title_full A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls
title_fullStr A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls
title_full_unstemmed A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls
title_short A Modular Cytokine Analysis Method Reveals Novel Associations With Clinical Phenotypes and Identifies Sets of Co-signaling Cytokines Across Influenza Natural Infection Cohorts and Healthy Controls
title_sort modular cytokine analysis method reveals novel associations with clinical phenotypes and identifies sets of co-signaling cytokines across influenza natural infection cohorts and healthy controls
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594355/
https://www.ncbi.nlm.nih.gov/pubmed/31275311
http://dx.doi.org/10.3389/fimmu.2019.01338
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