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High generation of reactive oxygen species from neutrophils in patients with severe COVID-19

Neutrophilia and an elevated neutrophil:lymphocyte ratio are both characteristic features of severe COVID-19 infection. However, functional neutrophil responses have been poorly investigated in this setting. We utilised a novel PMA-based stimulation assay to determine neutrophil-derived reactive oxy...

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Autores principales: Veenith, Tonny, Martin, Helena, Le Breuilly, Martin, Whitehouse, Tony, Gao-Smith, Fang, Duggal, Niharika, Lord, Janet M., Mian, Rubina, Sarphie, David, Moss, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9212205/
https://www.ncbi.nlm.nih.gov/pubmed/35729319
http://dx.doi.org/10.1038/s41598-022-13825-7
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author Veenith, Tonny
Martin, Helena
Le Breuilly, Martin
Whitehouse, Tony
Gao-Smith, Fang
Duggal, Niharika
Lord, Janet M.
Mian, Rubina
Sarphie, David
Moss, Paul
author_facet Veenith, Tonny
Martin, Helena
Le Breuilly, Martin
Whitehouse, Tony
Gao-Smith, Fang
Duggal, Niharika
Lord, Janet M.
Mian, Rubina
Sarphie, David
Moss, Paul
author_sort Veenith, Tonny
collection PubMed
description Neutrophilia and an elevated neutrophil:lymphocyte ratio are both characteristic features of severe COVID-19 infection. However, functional neutrophil responses have been poorly investigated in this setting. We utilised a novel PMA-based stimulation assay to determine neutrophil-derived reactive oxygen species (ROS) generation in patients with severe COVID-19 infection, non-COVID related sepsis and healthy study participants. ROS production was markedly elevated in COVID-19 patients with median values ninefold higher than in healthy controls and was particularly high in patients on mechanical ventilation. ROS generation correlated strongly with neutrophil count and elevated levels were also seen in patients with non-COVID related sepsis. Relative values, adjusted for neutrophil count, were high in both groups but extreme low or high values were seen in two patients who died shortly after testing, potentially indicating a predictive value for neutrophil function. Our results show that the high levels of neutrophils observed in patients with COVID-19 and sepsis exhibit functional capacity for ROS generation. This may contribute to the clinical features of acute disease and represents a potential novel target for therapeutic intervention.
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spelling pubmed-92122052022-06-22 High generation of reactive oxygen species from neutrophils in patients with severe COVID-19 Veenith, Tonny Martin, Helena Le Breuilly, Martin Whitehouse, Tony Gao-Smith, Fang Duggal, Niharika Lord, Janet M. Mian, Rubina Sarphie, David Moss, Paul Sci Rep Article Neutrophilia and an elevated neutrophil:lymphocyte ratio are both characteristic features of severe COVID-19 infection. However, functional neutrophil responses have been poorly investigated in this setting. We utilised a novel PMA-based stimulation assay to determine neutrophil-derived reactive oxygen species (ROS) generation in patients with severe COVID-19 infection, non-COVID related sepsis and healthy study participants. ROS production was markedly elevated in COVID-19 patients with median values ninefold higher than in healthy controls and was particularly high in patients on mechanical ventilation. ROS generation correlated strongly with neutrophil count and elevated levels were also seen in patients with non-COVID related sepsis. Relative values, adjusted for neutrophil count, were high in both groups but extreme low or high values were seen in two patients who died shortly after testing, potentially indicating a predictive value for neutrophil function. Our results show that the high levels of neutrophils observed in patients with COVID-19 and sepsis exhibit functional capacity for ROS generation. This may contribute to the clinical features of acute disease and represents a potential novel target for therapeutic intervention. Nature Publishing Group UK 2022-06-21 /pmc/articles/PMC9212205/ /pubmed/35729319 http://dx.doi.org/10.1038/s41598-022-13825-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Veenith, Tonny
Martin, Helena
Le Breuilly, Martin
Whitehouse, Tony
Gao-Smith, Fang
Duggal, Niharika
Lord, Janet M.
Mian, Rubina
Sarphie, David
Moss, Paul
High generation of reactive oxygen species from neutrophils in patients with severe COVID-19
title High generation of reactive oxygen species from neutrophils in patients with severe COVID-19
title_full High generation of reactive oxygen species from neutrophils in patients with severe COVID-19
title_fullStr High generation of reactive oxygen species from neutrophils in patients with severe COVID-19
title_full_unstemmed High generation of reactive oxygen species from neutrophils in patients with severe COVID-19
title_short High generation of reactive oxygen species from neutrophils in patients with severe COVID-19
title_sort high generation of reactive oxygen species from neutrophils in patients with severe covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9212205/
https://www.ncbi.nlm.nih.gov/pubmed/35729319
http://dx.doi.org/10.1038/s41598-022-13825-7
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