Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in Vivo

Background: It is important to study differential inflammatory cellular migration, particularly of eosinophils and neutrophils, in asthma and how this is influenced by environmental stimuli such as allergen exposure and the effects of anti asthma therapy. Methods: We isolated blood neutrophils and e...

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Main Authors: Joanna J. Lukawska, Lefteris Livieratos, Barbara M. Sawyer, Tak Lee, Michael O'Doherty, Philip J. Blower, Martin Kofi, James R. Ballinger, Christopher J. Corrigan, Gopinath Gnanasegaran, Ehsan Sharif-Paghaleh, Gregory E.D. Mullen
Format: Article
Language:English
Published: Elsevier 2014-12-01
Series:EBioMedicine
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396414000164
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language English
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author Joanna J. Lukawska
Lefteris Livieratos
Barbara M. Sawyer
Tak Lee
Michael O'Doherty
Philip J. Blower
Martin Kofi
James R. Ballinger
Christopher J. Corrigan
Gopinath Gnanasegaran
Ehsan Sharif-Paghaleh
Gregory E.D. Mullen
spellingShingle Joanna J. Lukawska
Lefteris Livieratos
Barbara M. Sawyer
Tak Lee
Michael O'Doherty
Philip J. Blower
Martin Kofi
James R. Ballinger
Christopher J. Corrigan
Gopinath Gnanasegaran
Ehsan Sharif-Paghaleh
Gregory E.D. Mullen
Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in Vivo
EBioMedicine
Asthma
Eosinophils
Neutrophils
Migration kinetics
Radioisotope
Allergen challenge
author_facet Joanna J. Lukawska
Lefteris Livieratos
Barbara M. Sawyer
Tak Lee
Michael O'Doherty
Philip J. Blower
Martin Kofi
James R. Ballinger
Christopher J. Corrigan
Gopinath Gnanasegaran
Ehsan Sharif-Paghaleh
Gregory E.D. Mullen
author_sort Joanna J. Lukawska
title Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in Vivo
title_short Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in Vivo
title_full Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in Vivo
title_fullStr Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in Vivo
title_full_unstemmed Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in Vivo
title_sort imaging inflammation in asthma: real time, differential tracking of human neutrophil and eosinophil migration in allergen challenged, atopic asthmatics in vivo
publisher Elsevier
series EBioMedicine
issn 2352-3964
publishDate 2014-12-01
description Background: It is important to study differential inflammatory cellular migration, particularly of eosinophils and neutrophils, in asthma and how this is influenced by environmental stimuli such as allergen exposure and the effects of anti asthma therapy. Methods: We isolated blood neutrophils and eosinophils from 12 atopic asthmatic human volunteers (Group 1 — four Early Allergic Responders unchallenged (EAR); Group 2 — four Early and Late Allergic Responders (LAR) challenged; Group 3 — four EAR and LAR challenged and treated with systemic corticosteroids) using cGMP CD16 CliniMACS. Cells were isolated prior to allergen challenge where applicable, labelled with 99mTc-HMPAO and then re-infused intravenously. The kinetics of cellular influx/efflux into the lungs and other organs were imaged via scintigraphy over 4 h, starting at 5 to 6 h following allergen challenge where applicable. Results: Neutrophils and eosinophils were isolated to a mean (SD) purity of 98.36% (1.09) and 96.31% (3.0), respectively. Asthmatic neutrophils were activated at baseline, mean (SD) CD11bHigh cells 46 (10.50) %. Isolation and radiolabelling significantly increased their activation to >98%. Eosinophils were not activated at baseline, CD69+ cells 1.9 (0.6) %, increasing to 38 (3.46) % following isolation and labelling. Analysis of the kinetics of net eosinophil and neutrophil lung influx/efflux conformed to a net exponential clearance with respective mean half times of clearance 6.98 (2.18) and 14.01 (2.63) minutes for Group 1, 6.03 (0.72) and 16.04 (2.0) minutes for Group 2 and 5.63 (1.20) and 14.56 (3.36) minutes for Group 3. These did not significantly differ between the three asthma groups (p > 0.05). Conclusions: Isolation and radiolabelling significantly increased activation of eosinophils (CD69) and completely activated neutrophils (CD11bHigh) in all asthma groups. Net lung neutrophil efflux was significantly slower than that of eosinophils in all asthma study groups. There was a trend for pre-treatment with systemic corticosteroids to reduce lung retention of eosinophils following allergen challenge.
topic Asthma
Eosinophils
Neutrophils
Migration kinetics
Radioisotope
Allergen challenge
url http://www.sciencedirect.com/science/article/pii/S2352396414000164
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spelling doaj-db5e7305c53c4d27937ec104ef3c74d82020-11-25T01:22:42ZengElsevierEBioMedicine2352-39642014-12-011217318010.1016/j.ebiom.2014.10.014Imaging Inflammation in Asthma: Real Time, Differential Tracking of Human Neutrophil and Eosinophil Migration in Allergen Challenged, Atopic Asthmatics in VivoJoanna J. Lukawska0Lefteris Livieratos1Barbara M. Sawyer2Tak Lee3Michael O'Doherty4Philip J. Blower5Martin Kofi6James R. Ballinger7Christopher J. Corrigan8Gopinath Gnanasegaran9Ehsan Sharif-Paghaleh10Gregory E.D. Mullen11Kings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKKings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKKings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKKing's College London, Department of Asthma, Allergy & Respiratory Science, 5th Floor, Tower Wing, Guy's Hospital, London SE1 9RT, UKKings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKKings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKDepartment of Nuclear Medicine, Guy's and St. Thomas' Hospitals, London SE1 9RT, UKKings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKKing's College London, Department of Asthma, Allergy & Respiratory Science, 5th Floor, Tower Wing, Guy's Hospital, London SE1 9RT, UKDepartment of Nuclear Medicine, Guy's and St. Thomas' Hospitals, London SE1 9RT, UKKings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKKings College London, Division of Imaging Sciences and Bioengineering, St. Thomas' Hospital, London SE1 7EH, UKBackground: It is important to study differential inflammatory cellular migration, particularly of eosinophils and neutrophils, in asthma and how this is influenced by environmental stimuli such as allergen exposure and the effects of anti asthma therapy. Methods: We isolated blood neutrophils and eosinophils from 12 atopic asthmatic human volunteers (Group 1 — four Early Allergic Responders unchallenged (EAR); Group 2 — four Early and Late Allergic Responders (LAR) challenged; Group 3 — four EAR and LAR challenged and treated with systemic corticosteroids) using cGMP CD16 CliniMACS. Cells were isolated prior to allergen challenge where applicable, labelled with 99mTc-HMPAO and then re-infused intravenously. The kinetics of cellular influx/efflux into the lungs and other organs were imaged via scintigraphy over 4 h, starting at 5 to 6 h following allergen challenge where applicable. Results: Neutrophils and eosinophils were isolated to a mean (SD) purity of 98.36% (1.09) and 96.31% (3.0), respectively. Asthmatic neutrophils were activated at baseline, mean (SD) CD11bHigh cells 46 (10.50) %. Isolation and radiolabelling significantly increased their activation to >98%. Eosinophils were not activated at baseline, CD69+ cells 1.9 (0.6) %, increasing to 38 (3.46) % following isolation and labelling. Analysis of the kinetics of net eosinophil and neutrophil lung influx/efflux conformed to a net exponential clearance with respective mean half times of clearance 6.98 (2.18) and 14.01 (2.63) minutes for Group 1, 6.03 (0.72) and 16.04 (2.0) minutes for Group 2 and 5.63 (1.20) and 14.56 (3.36) minutes for Group 3. These did not significantly differ between the three asthma groups (p > 0.05). Conclusions: Isolation and radiolabelling significantly increased activation of eosinophils (CD69) and completely activated neutrophils (CD11bHigh) in all asthma groups. Net lung neutrophil efflux was significantly slower than that of eosinophils in all asthma study groups. There was a trend for pre-treatment with systemic corticosteroids to reduce lung retention of eosinophils following allergen challenge.http://www.sciencedirect.com/science/article/pii/S2352396414000164AsthmaEosinophilsNeutrophilsMigration kineticsRadioisotopeAllergen challenge