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Residual lung abnormality following COVID-19 hospitalisation is characterised by biomarkers of epithelial injury

Residual lung abnormality following COVID-19 hospitalisation is characterised by biomarkers of epithelial injury
Residual lung abnormality following COVID-19 hospitalisation is characterised by biomarkers of epithelial injury

Background: long term respiratory symptoms are reported following recovery of acute COVID-19 infection and residual lung abnormalities (RLA) on follow-up thoracic computed tomography (CT) after COVID-19 hospitalisation have been observed. It is unknown whether RLA are associated with epithelial lung injury.

Methods: plasma was sampled from the observational Post HOSPitalisation-COVID cohort at five months post-hospitalisation. Epithelial injury biomarkers Krebs von den Lungen-6 (KL-6), matrix metalloproteinase 7 (MMP-7), surfactant protein-D (SP-D) and surfactant protein-A (SP-A) were assayed. In those without follow-up CT, RLA at-risk was defined by percent predicted DL CO <80% and/or abnormal chest X-ray, otherwise they were considered low-risk. Follow-up CT RLA was defined as combined involvement of ground glass opacity and reticulation ≥10%. 

Findings: a total of 957 people were included, 846 people with no CT (at-risk n = 103; 12.2%), 111 people with follow-up CT (RLA ≥10% n = 85; 76.6%). All epithelial injury biomarkers were significantly elevated in people at-risk of RLA compared with low-risk. KL-6 and MMP-7 were significantly higher in people with ≥10% RLA than those with <10%, SP-D and SP-A did not reach significance. SP-D and SP-A were associated with percent involvement of reticulation (3.22%, 95% CI 1.19–5.24; 3.03%, 95% CI 0.76–5.30, respectively). 

Interpretation: RLA after acute COVID-19 infection were consistent with elevated epithelial injury biomarkers and pro-fibrotic signalling. Future studies should address the temporal association between fibrotic biomarkers and resolution or progression of radiological involvement. 

Funding: MRC-UK Research and Innovation and National Institute for Health Research (NIHR) rapid response panel to tackle COVID-19 (MR/V027859/1; COV0319; MR/W006111/1).

Biomarker, COVID-19, Epithelial, Hospitalisation, Lung injury
2352-3964
Stewart, Iain
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Jacob, Joseph
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Porter, Joanna C.
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Liu, Bin
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Tatler, Amanda L.
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Gomez, Nancy
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Allen, Richard J.
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Blaikley, John F.
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Chaudhuri, Nazia
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Denneny, Emma
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Johnson, Simon
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Jones, Mark G.
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Khan, Fasihul
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Mehta, Puja
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Mitchell, Jane
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Molyneaux, Philip L
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Pearl, John E
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Piper Hanley, Karen
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Platé, Manuela
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Quinn, Valerie
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Rivera-Ortega, Pilar
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Saunders, Laura C.
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Smith, David J.F.
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Spears, Mark
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Spencer, Lisa G.
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Stanel, Stefan C.
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Thompson, A.A. Roger
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Walsh, Simon
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Wild, Jim M.
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Wootton, Dan G.
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Docherty, Annemarie B.
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Gleeson, Fergus
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Greenhalf, William
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Harrison, Ewen M.
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Lone, Nazir
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Quint, Jennifer
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Maslova, Anastasia
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Pohl, Moritz
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Richardson, Matthew
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PHOSP-COVID Collaborative Group and the UKILD Consortium
Stewart, Iain
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Jacob, Joseph
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Porter, Joanna C.
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Liu, Bin
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Tatler, Amanda L.
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Gomez, Nancy
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Pugh, Matthew R.
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John, Alison E.
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Allen, Richard J.
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Blaikley, John F.
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Chaudhuri, Nazia
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Denneny, Emma
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Fabbri, Laura
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George, Peter M.
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Guillen-Guio, Beatriz
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Gooptu, Bibek
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Hall, Ian P
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Khan, Fasihul
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Mehta, Puja
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Mitchell, Jane
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Molyneaux, Philip L
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Pearl, John E
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Piper Hanley, Karen
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Platé, Manuela
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Quinn, Valerie
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Rivera-Ortega, Pilar
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Spears, Mark
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Stanel, Stefan C.
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Thompson, A.A. Roger
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Walsh, Simon
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Wild, Jim M.
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Wootton, Dan G.
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Docherty, Annemarie B.
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Gleeson, Fergus
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Greenhalf, William
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Harrison, Ewen M.
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Lone, Nazir
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Quint, Jennifer
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Maslova, Anastasia
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Stewart, Iain, Jacob, Joseph, Porter, Joanna C. and Jones, Mark G. , PHOSP-COVID Collaborative Group and the UKILD Consortium (2026) Residual lung abnormality following COVID-19 hospitalisation is characterised by biomarkers of epithelial injury. EBioMedicine, 124, [106134]. (doi:10.1016/j.ebiom.2026.106134).

Record type: Article

Abstract

Background: long term respiratory symptoms are reported following recovery of acute COVID-19 infection and residual lung abnormalities (RLA) on follow-up thoracic computed tomography (CT) after COVID-19 hospitalisation have been observed. It is unknown whether RLA are associated with epithelial lung injury.

Methods: plasma was sampled from the observational Post HOSPitalisation-COVID cohort at five months post-hospitalisation. Epithelial injury biomarkers Krebs von den Lungen-6 (KL-6), matrix metalloproteinase 7 (MMP-7), surfactant protein-D (SP-D) and surfactant protein-A (SP-A) were assayed. In those without follow-up CT, RLA at-risk was defined by percent predicted DL CO <80% and/or abnormal chest X-ray, otherwise they were considered low-risk. Follow-up CT RLA was defined as combined involvement of ground glass opacity and reticulation ≥10%. 

Findings: a total of 957 people were included, 846 people with no CT (at-risk n = 103; 12.2%), 111 people with follow-up CT (RLA ≥10% n = 85; 76.6%). All epithelial injury biomarkers were significantly elevated in people at-risk of RLA compared with low-risk. KL-6 and MMP-7 were significantly higher in people with ≥10% RLA than those with <10%, SP-D and SP-A did not reach significance. SP-D and SP-A were associated with percent involvement of reticulation (3.22%, 95% CI 1.19–5.24; 3.03%, 95% CI 0.76–5.30, respectively). 

Interpretation: RLA after acute COVID-19 infection were consistent with elevated epithelial injury biomarkers and pro-fibrotic signalling. Future studies should address the temporal association between fibrotic biomarkers and resolution or progression of radiological involvement. 

Funding: MRC-UK Research and Innovation and National Institute for Health Research (NIHR) rapid response panel to tackle COVID-19 (MR/V027859/1; COV0319; MR/W006111/1).

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Accepted/In Press date: 9 January 2026
e-pub ahead of print date: 24 January 2026
Published date: February 2026
Keywords: Biomarker, COVID-19, Epithelial, Hospitalisation, Lung injury

Identifiers

Local EPrints ID: 511382
URI: http://eprints.soton.ac.uk/id/eprint/511382
ISSN: 2352-3964
PURE UUID: 8b43bdc2-e66e-429e-97f9-c0ba3650910b

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Date deposited: 13 May 2026 16:46
Last modified: 13 May 2026 16:47

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Contributors

Author: Iain Stewart
Author: Joseph Jacob
Author: Joanna C. Porter
Author: Bin Liu
Author: Amanda L. Tatler
Author: Nancy Gomez
Author: Matthew R. Pugh
Author: Alison E. John
Author: Richard J. Allen
Author: John F. Blaikley
Author: Nazia Chaudhuri
Author: Emma Denneny
Author: Laura Fabbri
Author: Peter M. George
Author: Beatriz Guillen-Guio
Author: Bibek Gooptu
Author: Ian P Hall
Author: Ling Pei Ho
Author: Ian Jarrold
Author: Simon Johnson
Author: Mark G. Jones
Author: Fasihul Khan
Author: Puja Mehta
Author: Jane Mitchell
Author: Philip L Molyneaux
Author: John E Pearl
Author: Karen Piper Hanley
Author: Manuela Platé
Author: Valerie Quinn
Author: Pilar Rivera-Ortega
Author: Laura C. Saunders
Author: David J.F. Smith
Author: Mark Spears
Author: Lisa G. Spencer
Author: Stefan C. Stanel
Author: A.A. Roger Thompson
Author: Simon Walsh
Author: Jim M. Wild
Author: Dan G. Wootton
Author: Annemarie B. Docherty
Author: Fergus Gleeson
Author: William Greenhalf
Author: Ewen M. Harrison
Author: Nazir Lone
Author: Jennifer Quint
Author: Anastasia Maslova
Author: Moritz Pohl
Author: Adam Stephens
Author: Simon Young
Author: Matthew Richardson
Corporate Author: PHOSP-COVID Collaborative Group and the UKILD Consortium

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