Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783580811786715136 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7482580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhuyanfangpeipei cytofmasscytometryrevealsphenotypicallydistincthumanbloodneutrophilpopulationsdifferentiallycorrelatedwithmelanomastage AT eggerttobias cytofmasscytometryrevealsphenotypicallydistincthumanbloodneutrophilpopulationsdifferentiallycorrelatedwithmelanomastage AT araujodanielj cytofmasscytometryrevealsphenotypicallydistincthumanbloodneutrophilpopulationsdifferentiallycorrelatedwithmelanomastage AT vijayanandpandurangan cytofmasscytometryrevealsphenotypicallydistincthumanbloodneutrophilpopulationsdifferentiallycorrelatedwithmelanomastage AT ottensmeierchristianhermann cytofmasscytometryrevealsphenotypicallydistincthumanbloodneutrophilpopulationsdifferentiallycorrelatedwithmelanomastage AT hedrickcatherinec cytofmasscytometryrevealsphenotypicallydistincthumanbloodneutrophilpopulationsdifferentiallycorrelatedwithmelanomastage |