Proteomic blood profiling in mild, severe and critical COVID-19 patients

Abstract The recent SARS-CoV-2 pandemic manifests itself as a mild respiratory tract infection in most individuals, leading to COVID-19 disease. However, in some infected individuals, this can progress to severe pneumonia and acute respiratory distress syndrome (ARDS), leading to multi-organ failure...

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Autores principales: Hamel Patel, Nicholas J. Ashton, Richard J. B. Dobson, Lars-Magnus Andersson, Aylin Yilmaz, Kaj Blennow, Magnus Gisslen, Henrik Zetterberg
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/85741894ac0a46b49312bed2836a1782
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spelling oai:doaj.org-article:85741894ac0a46b49312bed2836a17822021-12-02T17:05:46ZProteomic blood profiling in mild, severe and critical COVID-19 patients10.1038/s41598-021-85877-02045-2322https://doaj.org/article/85741894ac0a46b49312bed2836a17822021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-85877-0https://doaj.org/toc/2045-2322Abstract The recent SARS-CoV-2 pandemic manifests itself as a mild respiratory tract infection in most individuals, leading to COVID-19 disease. However, in some infected individuals, this can progress to severe pneumonia and acute respiratory distress syndrome (ARDS), leading to multi-organ failure and death. This study explores the proteomic differences between mild, severe, and critical COVID-19 positive patients to further understand the disease progression, identify proteins associated with disease severity, and identify potential therapeutic targets. Blood protein profiling was performed on 59 COVID-19 mild (n = 26), severe (n = 9) or critical (n = 24) cases and 28 controls using the OLINK inflammation, autoimmune, cardiovascular and neurology panels. Differential expression analysis was performed within and between disease groups to generate nine different analyses. From the 368 proteins measured per individual, more than 75% were observed to be significantly perturbed in COVID-19 cases. Six proteins (IL6, CKAP4, Gal-9, IL-1ra, LILRB4 and PD-L1) were identified to be associated with disease severity. The results have been made readily available through an interactive web-based application for instant data exploration and visualization, and can be accessed at https://phidatalab-shiny.rosalind.kcl.ac.uk/COVID19/ . Our results demonstrate that dynamic changes in blood proteins associated with disease severity can potentially be used as early biomarkers to monitor disease severity in COVID-19 and serve as potential therapeutic targets.Hamel PatelNicholas J. AshtonRichard J. B. DobsonLars-Magnus AnderssonAylin YilmazKaj BlennowMagnus GisslenHenrik ZetterbergNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hamel Patel
Nicholas J. Ashton
Richard J. B. Dobson
Lars-Magnus Andersson
Aylin Yilmaz
Kaj Blennow
Magnus Gisslen
Henrik Zetterberg
Proteomic blood profiling in mild, severe and critical COVID-19 patients
description Abstract The recent SARS-CoV-2 pandemic manifests itself as a mild respiratory tract infection in most individuals, leading to COVID-19 disease. However, in some infected individuals, this can progress to severe pneumonia and acute respiratory distress syndrome (ARDS), leading to multi-organ failure and death. This study explores the proteomic differences between mild, severe, and critical COVID-19 positive patients to further understand the disease progression, identify proteins associated with disease severity, and identify potential therapeutic targets. Blood protein profiling was performed on 59 COVID-19 mild (n = 26), severe (n = 9) or critical (n = 24) cases and 28 controls using the OLINK inflammation, autoimmune, cardiovascular and neurology panels. Differential expression analysis was performed within and between disease groups to generate nine different analyses. From the 368 proteins measured per individual, more than 75% were observed to be significantly perturbed in COVID-19 cases. Six proteins (IL6, CKAP4, Gal-9, IL-1ra, LILRB4 and PD-L1) were identified to be associated with disease severity. The results have been made readily available through an interactive web-based application for instant data exploration and visualization, and can be accessed at https://phidatalab-shiny.rosalind.kcl.ac.uk/COVID19/ . Our results demonstrate that dynamic changes in blood proteins associated with disease severity can potentially be used as early biomarkers to monitor disease severity in COVID-19 and serve as potential therapeutic targets.
format article
author Hamel Patel
Nicholas J. Ashton
Richard J. B. Dobson
Lars-Magnus Andersson
Aylin Yilmaz
Kaj Blennow
Magnus Gisslen
Henrik Zetterberg
author_facet Hamel Patel
Nicholas J. Ashton
Richard J. B. Dobson
Lars-Magnus Andersson
Aylin Yilmaz
Kaj Blennow
Magnus Gisslen
Henrik Zetterberg
author_sort Hamel Patel
title Proteomic blood profiling in mild, severe and critical COVID-19 patients
title_short Proteomic blood profiling in mild, severe and critical COVID-19 patients
title_full Proteomic blood profiling in mild, severe and critical COVID-19 patients
title_fullStr Proteomic blood profiling in mild, severe and critical COVID-19 patients
title_full_unstemmed Proteomic blood profiling in mild, severe and critical COVID-19 patients
title_sort proteomic blood profiling in mild, severe and critical covid-19 patients
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/85741894ac0a46b49312bed2836a1782
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