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Activated neutrophil fluorescent imaging technique for human lungs
Neutrophil activation is an integral process to acute inflammation and is associated with adverse clinical sequelae. Identification of neutrophil activation in real time in the lungs of patients may permit biological stratification of patients in otherwise heterogenous cohorts typically defined by c...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806726/ https://www.ncbi.nlm.nih.gov/pubmed/33441792 http://dx.doi.org/10.1038/s41598-020-80083-w |
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author | Craven, Thomas H. Walton, Tashfeen Akram, Ahsan R. Scholefield, Emma McDonald, Neil Marshall, Adam D.L. Humphries, Duncan C. Mills, Bethany Campbell, Thane A. Bruce, Annya Mair, Joanne Dear, James W. Newby, David E. Hill, Adam T. Walsh, Timothy S. Haslett, Chris Dhaliwal, Kevin |
author_facet | Craven, Thomas H. Walton, Tashfeen Akram, Ahsan R. Scholefield, Emma McDonald, Neil Marshall, Adam D.L. Humphries, Duncan C. Mills, Bethany Campbell, Thane A. Bruce, Annya Mair, Joanne Dear, James W. Newby, David E. Hill, Adam T. Walsh, Timothy S. Haslett, Chris Dhaliwal, Kevin |
author_sort | Craven, Thomas H. |
collection | PubMed |
description | Neutrophil activation is an integral process to acute inflammation and is associated with adverse clinical sequelae. Identification of neutrophil activation in real time in the lungs of patients may permit biological stratification of patients in otherwise heterogenous cohorts typically defined by clinical criteria. No methods for identifying neutrophil activation in real time in the lungs of patients currently exist. We developed a bespoke molecular imaging probe targeting three characteristic signatures of neutrophil activation: pinocytosis, phagosomal alkalinisation, and human neutrophil elastase (HNE) activity. The probe functioned as designed in vitro and ex vivo. We evaluated optical endomicroscopy imaging of neutrophil activity using the probe in real-time at the bedside of healthy volunteers, patients with bronchiectasis, and critically unwell mechanically ventilated patients. We detected a range of imaging responses in vivo reflecting heterogeneity of condition and severity. We corroborated optical signal was due to probe function and neutrophil activation. |
format | Online Article Text |
id | pubmed-7806726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78067262021-01-14 Activated neutrophil fluorescent imaging technique for human lungs Craven, Thomas H. Walton, Tashfeen Akram, Ahsan R. Scholefield, Emma McDonald, Neil Marshall, Adam D.L. Humphries, Duncan C. Mills, Bethany Campbell, Thane A. Bruce, Annya Mair, Joanne Dear, James W. Newby, David E. Hill, Adam T. Walsh, Timothy S. Haslett, Chris Dhaliwal, Kevin Sci Rep Article Neutrophil activation is an integral process to acute inflammation and is associated with adverse clinical sequelae. Identification of neutrophil activation in real time in the lungs of patients may permit biological stratification of patients in otherwise heterogenous cohorts typically defined by clinical criteria. No methods for identifying neutrophil activation in real time in the lungs of patients currently exist. We developed a bespoke molecular imaging probe targeting three characteristic signatures of neutrophil activation: pinocytosis, phagosomal alkalinisation, and human neutrophil elastase (HNE) activity. The probe functioned as designed in vitro and ex vivo. We evaluated optical endomicroscopy imaging of neutrophil activity using the probe in real-time at the bedside of healthy volunteers, patients with bronchiectasis, and critically unwell mechanically ventilated patients. We detected a range of imaging responses in vivo reflecting heterogeneity of condition and severity. We corroborated optical signal was due to probe function and neutrophil activation. Nature Publishing Group UK 2021-01-13 /pmc/articles/PMC7806726/ /pubmed/33441792 http://dx.doi.org/10.1038/s41598-020-80083-w Text en © The Author(s) 2021 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/. |
spellingShingle | Article Craven, Thomas H. Walton, Tashfeen Akram, Ahsan R. Scholefield, Emma McDonald, Neil Marshall, Adam D.L. Humphries, Duncan C. Mills, Bethany Campbell, Thane A. Bruce, Annya Mair, Joanne Dear, James W. Newby, David E. Hill, Adam T. Walsh, Timothy S. Haslett, Chris Dhaliwal, Kevin Activated neutrophil fluorescent imaging technique for human lungs |
title | Activated neutrophil fluorescent imaging technique for human lungs |
title_full | Activated neutrophil fluorescent imaging technique for human lungs |
title_fullStr | Activated neutrophil fluorescent imaging technique for human lungs |
title_full_unstemmed | Activated neutrophil fluorescent imaging technique for human lungs |
title_short | Activated neutrophil fluorescent imaging technique for human lungs |
title_sort | activated neutrophil fluorescent imaging technique for human lungs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806726/ https://www.ncbi.nlm.nih.gov/pubmed/33441792 http://dx.doi.org/10.1038/s41598-020-80083-w |
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