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CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage

BACKGROUND: Understanding neutrophil heterogeneity and its relationship to disease progression has become a recent focus of cancer research. Indeed, several studies have identified neutrophil subpopulations associated with protumoral or antitumoral functions. However, this work has been hindered by...

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Autores principales: Zhu, Yanfang Peipei, Eggert, Tobias, Araujo, Daniel J, Vijayanand, Pandurangan, Ottensmeier, Christian Hermann, Hedrick, Catherine C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482580/
https://www.ncbi.nlm.nih.gov/pubmed/32912924
http://dx.doi.org/10.1136/jitc-2019-000473
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author Zhu, Yanfang Peipei
Eggert, Tobias
Araujo, Daniel J
Vijayanand, Pandurangan
Ottensmeier, Christian Hermann
Hedrick, Catherine C
author_facet Zhu, Yanfang Peipei
Eggert, Tobias
Araujo, Daniel J
Vijayanand, Pandurangan
Ottensmeier, Christian Hermann
Hedrick, Catherine C
author_sort Zhu, Yanfang Peipei
collection PubMed
description BACKGROUND: Understanding neutrophil heterogeneity and its relationship to disease progression has become a recent focus of cancer research. Indeed, several studies have identified neutrophil subpopulations associated with protumoral or antitumoral functions. However, this work has been hindered by a lack of widely accepted markers with which to define neutrophil subpopulations. METHODS: To identify markers of neutrophil heterogeneity in cancer, we used single-cell cytometry by time-of-flight (CyTOF) coupled with high-dimensional analysis on blood samples from treatment-naïve patients with melanoma. RESULTS: Our efforts allowed us to identify seven blood neutrophil clusters, including two previously identified individual populations. Interrogation of these neutrophil subpopulations revealed a positive trend between specific clusters and disease stage. Finally, we recapitulated these seven blood neutrophil populations via flow cytometry and found that they exhibited diverse capacities for phagocytosis and reactive oxygen species production in vitro. CONCLUSIONS: Our data provide a refined consensus on neutrophil heterogeneity markers, enabling a prospective functional evaluation in patients with solid tumors.
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spelling pubmed-74825802020-09-18 CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage Zhu, Yanfang Peipei Eggert, Tobias Araujo, Daniel J Vijayanand, Pandurangan Ottensmeier, Christian Hermann Hedrick, Catherine C J Immunother Cancer Immunotherapy Biomarkers BACKGROUND: Understanding neutrophil heterogeneity and its relationship to disease progression has become a recent focus of cancer research. Indeed, several studies have identified neutrophil subpopulations associated with protumoral or antitumoral functions. However, this work has been hindered by a lack of widely accepted markers with which to define neutrophil subpopulations. METHODS: To identify markers of neutrophil heterogeneity in cancer, we used single-cell cytometry by time-of-flight (CyTOF) coupled with high-dimensional analysis on blood samples from treatment-naïve patients with melanoma. RESULTS: Our efforts allowed us to identify seven blood neutrophil clusters, including two previously identified individual populations. Interrogation of these neutrophil subpopulations revealed a positive trend between specific clusters and disease stage. Finally, we recapitulated these seven blood neutrophil populations via flow cytometry and found that they exhibited diverse capacities for phagocytosis and reactive oxygen species production in vitro. CONCLUSIONS: Our data provide a refined consensus on neutrophil heterogeneity markers, enabling a prospective functional evaluation in patients with solid tumors. BMJ Publishing Group 2020-09-09 /pmc/articles/PMC7482580/ /pubmed/32912924 http://dx.doi.org/10.1136/jitc-2019-000473 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See https://creativecommons.org/licenses/by/4.0/.
spellingShingle Immunotherapy Biomarkers
Zhu, Yanfang Peipei
Eggert, Tobias
Araujo, Daniel J
Vijayanand, Pandurangan
Ottensmeier, Christian Hermann
Hedrick, Catherine C
CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage
title CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage
title_full CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage
title_fullStr CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage
title_full_unstemmed CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage
title_short CyTOF mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage
title_sort cytof mass cytometry reveals phenotypically distinct human blood neutrophil populations differentially correlated with melanoma stage
topic Immunotherapy Biomarkers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482580/
https://www.ncbi.nlm.nih.gov/pubmed/32912924
http://dx.doi.org/10.1136/jitc-2019-000473
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