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Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus

BACKGROUND: Evidence suggests that patients critically ill with COVID-19 have a dysregulated host immune response that contributes to end-organ damage. Extracorporeal membrane oxygenation (ECMO) has been used in this population with varying degrees of success. This study was performed to evaluate th...

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Autores principales: Smith, Deane E., Goparaju, Chandra M., Pass, Harvey I., James, Les, Alimi, Marjan, Chang, Stephanie, Grossi, Eugene A., Moazami, Nader, Galloway, Aubrey C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Inc. on behalf of The Society of Thoracic Surgeons. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103524/
https://www.ncbi.nlm.nih.gov/pubmed/37360841
http://dx.doi.org/10.1016/j.atssr.2023.04.003
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author Smith, Deane E.
Goparaju, Chandra M.
Pass, Harvey I.
James, Les
Alimi, Marjan
Chang, Stephanie
Grossi, Eugene A.
Moazami, Nader
Galloway, Aubrey C.
author_facet Smith, Deane E.
Goparaju, Chandra M.
Pass, Harvey I.
James, Les
Alimi, Marjan
Chang, Stephanie
Grossi, Eugene A.
Moazami, Nader
Galloway, Aubrey C.
author_sort Smith, Deane E.
collection PubMed
description BACKGROUND: Evidence suggests that patients critically ill with COVID-19 have a dysregulated host immune response that contributes to end-organ damage. Extracorporeal membrane oxygenation (ECMO) has been used in this population with varying degrees of success. This study was performed to evaluate the impact of ECMO on the host immunotranscriptomic response in these patients. METHODS: Eleven patients critically ill with COVID-19 requiring ECMO underwent an analysis of cytokines and immunotranscriptomic pathways before ECMO (T1), after ECMO for 24 hours (T2), and 2 hours after ECMO decannulation (T3). A Multiplex Human Cytokine panel was used to identify cytokine changes, and immunotranscriptomic changes in peripheral leukocytes were evaluated by PAXgene and NanoString nCounter. RESULTS: Differential gene expression of 11 host immune genes was noted at T2 compared with T1. The most significant genes were MD2 and MRC1, which code for binding ligands for the activation of toll-like receptors 2 and 4. Reactome analyses of differential gene expression demonstrated an impact on many of the body’s most important immune inflammatory pathways. CONCLUSIONS: These findings suggest a temporal impact of ECMO on the host immunotranscriptomic response in patients critically ill with COVID-19.
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spelling pubmed-101035242023-04-17 Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus Smith, Deane E. Goparaju, Chandra M. Pass, Harvey I. James, Les Alimi, Marjan Chang, Stephanie Grossi, Eugene A. Moazami, Nader Galloway, Aubrey C. Ann Thorac Surg Short Rep Science & Research Methods BACKGROUND: Evidence suggests that patients critically ill with COVID-19 have a dysregulated host immune response that contributes to end-organ damage. Extracorporeal membrane oxygenation (ECMO) has been used in this population with varying degrees of success. This study was performed to evaluate the impact of ECMO on the host immunotranscriptomic response in these patients. METHODS: Eleven patients critically ill with COVID-19 requiring ECMO underwent an analysis of cytokines and immunotranscriptomic pathways before ECMO (T1), after ECMO for 24 hours (T2), and 2 hours after ECMO decannulation (T3). A Multiplex Human Cytokine panel was used to identify cytokine changes, and immunotranscriptomic changes in peripheral leukocytes were evaluated by PAXgene and NanoString nCounter. RESULTS: Differential gene expression of 11 host immune genes was noted at T2 compared with T1. The most significant genes were MD2 and MRC1, which code for binding ligands for the activation of toll-like receptors 2 and 4. Reactome analyses of differential gene expression demonstrated an impact on many of the body’s most important immune inflammatory pathways. CONCLUSIONS: These findings suggest a temporal impact of ECMO on the host immunotranscriptomic response in patients critically ill with COVID-19. The Author(s). Published by Elsevier Inc. on behalf of The Society of Thoracic Surgeons. 2023-04-14 /pmc/articles/PMC10103524/ /pubmed/37360841 http://dx.doi.org/10.1016/j.atssr.2023.04.003 Text en © 2023 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Science & Research Methods
Smith, Deane E.
Goparaju, Chandra M.
Pass, Harvey I.
James, Les
Alimi, Marjan
Chang, Stephanie
Grossi, Eugene A.
Moazami, Nader
Galloway, Aubrey C.
Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus
title Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus
title_full Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus
title_fullStr Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus
title_full_unstemmed Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus
title_short Extracorporeal Membrane Oxygenation Impact on Host Transcriptomic Response in Severe Coronavirus
title_sort extracorporeal membrane oxygenation impact on host transcriptomic response in severe coronavirus
topic Science & Research Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103524/
https://www.ncbi.nlm.nih.gov/pubmed/37360841
http://dx.doi.org/10.1016/j.atssr.2023.04.003
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