Table 2 Proteins dysregulated in critical disease and modulated by imatinib

From: Longitudinal plasma proteomics reveals biomarkers of alveolar-capillary barrier disruption in critically ill COVID-19 patients

Protein

GeneID

Change in critical disease

Imatinib effect

Angiopoietin-related protein 3

ANGPTL3

Increase

Decrease

Collagen alpha-1(XXVIII) chain

COL28A1

Increase

Decrease

Collagen alpha-1(I) chain:C-term propeptide

COL1A1

Increase

Decrease

Collagen alpha-3(VI) chain:Bovine pancreatic trypsin inhibitor/Kunitz inhibitor domain, isoform 1

COL6A3

Increase

Decrease

Serine protease 27

PRSS27

Decrease

Increase

Serpin B13

SERPINB13

Decrease

Increase

Collagen Type III

COL3A1

Increase

Decrease

Calcipressin-3

RCAN3

Increase

Decrease

Collagen alpha-1(V) chain

COL5A1

Increase

Decrease

Interleukin-6

IL6

Increase

Decrease

Luteinizing hormone

CGA|LHB

Decrease

Increase

Tumour necrosis factor ligand superfamily member 15

TNFSF15

Increase

Decrease

Biglycan

BGN

Increase

Decrease

Thrombospondin-2

THBS2

Increase

Decrease

Urokinase-type plasminogen activator

PLAU

Increase

Decrease

Repulsive guidance molecule A

RGMA

Decrease

Increase

Apolipoprotein D

APOD

Decrease

Increase

Olfactomedin-like protein 3

OLFML3

Increase

Decrease

Platelet-derived growth factor D

PDGFD

Decrease

Increase

  1. Proteins that changed over time in patients who developed critical illness and were modulated by imatinib treatment are shown. The direction and significance levels were established in linear mixed models. This was achieved by applying an interaction term between time and critical disease, and time and imatinib treatment, respectively. Benjamini-Hochberg correction was applied to correct for multiple testing with a false discovery rate (FDR) of 0.05. A complete overview of changes over time of alle proteins are presented in Supplementary data SDF4 and SDF7.