Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.

Coronavirus disease (COVID)-19, as a result of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection, has been the direct cause of over 2.2 million deaths worldwide. A timely coordinated host-immune response represents the leading driver for restraining SARS-CoV-2 infection. Indeed,...

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Main Authors: Francesco Palmas, Jennifer Clarke, Romain A Colas, Esteban A Gomez, Aoife Keogh, Maria Boylan, Natalie McEvoy, Oliver J McElvaney, Oisin McElvaney, Razi Alalqam, Noel G McElvaney, Gerard F Curley, Jesmond Dalli
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0256226
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author Francesco Palmas
Jennifer Clarke
Romain A Colas
Esteban A Gomez
Aoife Keogh
Maria Boylan
Natalie McEvoy
Oliver J McElvaney
Oisin McElvaney
Razi Alalqam
Noel G McElvaney
Gerard F Curley
Jesmond Dalli
author_facet Francesco Palmas
Jennifer Clarke
Romain A Colas
Esteban A Gomez
Aoife Keogh
Maria Boylan
Natalie McEvoy
Oliver J McElvaney
Oisin McElvaney
Razi Alalqam
Noel G McElvaney
Gerard F Curley
Jesmond Dalli
author_sort Francesco Palmas
collection DOAJ
description Coronavirus disease (COVID)-19, as a result of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection, has been the direct cause of over 2.2 million deaths worldwide. A timely coordinated host-immune response represents the leading driver for restraining SARS-CoV-2 infection. Indeed, several studies have described dysregulated immunity as the crucial determinant for critical illness and the failure of viral control. Improved understanding and management of COVID-19 could greatly reduce the mortality and morbidity caused by SARS-CoV-2. One aspect of the immune response that has to date been understudied is whether lipid mediator production is dysregulated in critically ill patients. In the present study, plasma from COVID-19 patients with either severe disease and those that were critically ill was collected and lipid mediator profiles were determined using liquid chromatography tandem mass spectrometry. Results from these studies indicated that plasma concentrations of both pro-inflammatory and pro-resolving lipid mediator were reduced in critically ill patients when compared with those with severe disease. Furthermore, plasma concentrations of a select group of mediators that included the specialized pro-resolving mediators (SPM) Resolvin (Rv) D1 and RvE4 were diagnostic of disease severity. Interestingly, peripheral blood SPM concentrations were also linked with outcome in critically ill patients, where we observed reduced overall concentrations of these mediators in those patients that did not survive. Together the present findings establish a link between plasma lipid mediators and disease severity in patients with COVID-19 and indicate that plasma SPM concentrations may be linked with survival in these patients.
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spelling doaj.art-7f9563a15fbe4d7892bc459854e426852022-12-21T19:54:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01168e025622610.1371/journal.pone.0256226Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.Francesco PalmasJennifer ClarkeRomain A ColasEsteban A GomezAoife KeoghMaria BoylanNatalie McEvoyOliver J McElvaneyOisin McElvaneyRazi AlalqamNoel G McElvaneyGerard F CurleyJesmond DalliCoronavirus disease (COVID)-19, as a result of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection, has been the direct cause of over 2.2 million deaths worldwide. A timely coordinated host-immune response represents the leading driver for restraining SARS-CoV-2 infection. Indeed, several studies have described dysregulated immunity as the crucial determinant for critical illness and the failure of viral control. Improved understanding and management of COVID-19 could greatly reduce the mortality and morbidity caused by SARS-CoV-2. One aspect of the immune response that has to date been understudied is whether lipid mediator production is dysregulated in critically ill patients. In the present study, plasma from COVID-19 patients with either severe disease and those that were critically ill was collected and lipid mediator profiles were determined using liquid chromatography tandem mass spectrometry. Results from these studies indicated that plasma concentrations of both pro-inflammatory and pro-resolving lipid mediator were reduced in critically ill patients when compared with those with severe disease. Furthermore, plasma concentrations of a select group of mediators that included the specialized pro-resolving mediators (SPM) Resolvin (Rv) D1 and RvE4 were diagnostic of disease severity. Interestingly, peripheral blood SPM concentrations were also linked with outcome in critically ill patients, where we observed reduced overall concentrations of these mediators in those patients that did not survive. Together the present findings establish a link between plasma lipid mediators and disease severity in patients with COVID-19 and indicate that plasma SPM concentrations may be linked with survival in these patients.https://doi.org/10.1371/journal.pone.0256226
spellingShingle Francesco Palmas
Jennifer Clarke
Romain A Colas
Esteban A Gomez
Aoife Keogh
Maria Boylan
Natalie McEvoy
Oliver J McElvaney
Oisin McElvaney
Razi Alalqam
Noel G McElvaney
Gerard F Curley
Jesmond Dalli
Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.
PLoS ONE
title Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.
title_full Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.
title_fullStr Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.
title_full_unstemmed Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.
title_short Dysregulated plasma lipid mediator profiles in critically ill COVID-19 patients.
title_sort dysregulated plasma lipid mediator profiles in critically ill covid 19 patients
url https://doi.org/10.1371/journal.pone.0256226
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