Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS. / Jonassen, Trine B.; Jørgensen, Sofie E.; Mitchell, Nikki H.; Mogensen, Trine H.; Berg, Ronan M. G.; Ronit, Andreas; Plovsing, Ronni R.

I: Frontiers in Immunology, Bind 15, 1353012, 2024.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jonassen, TB, Jørgensen, SE, Mitchell, NH, Mogensen, TH, Berg, RMG, Ronit, A & Plovsing, RR 2024, 'Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS', Frontiers in Immunology, bind 15, 1353012. https://doi.org/10.3389/fimmu.2024.1353012

APA

Jonassen, T. B., Jørgensen, S. E., Mitchell, N. H., Mogensen, T. H., Berg, R. M. G., Ronit, A., & Plovsing, R. R. (2024). Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS. Frontiers in Immunology, 15, [1353012]. https://doi.org/10.3389/fimmu.2024.1353012

Vancouver

Jonassen TB, Jørgensen SE, Mitchell NH, Mogensen TH, Berg RMG, Ronit A o.a. Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS. Frontiers in Immunology. 2024;15. 1353012. https://doi.org/10.3389/fimmu.2024.1353012

Author

Jonassen, Trine B. ; Jørgensen, Sofie E. ; Mitchell, Nikki H. ; Mogensen, Trine H. ; Berg, Ronan M. G. ; Ronit, Andreas ; Plovsing, Ronni R. / Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS. I: Frontiers in Immunology. 2024 ; Bind 15.

Bibtex

@article{6fd7c4c0ed6a4a84bcb967c8f8b14c8f,
title = "Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS",
abstract = "Background: Type I interferon (IFN-I) and IFN autoantibodies play a crucial role in controlling SARS-CoV-2 infection. The levels of these mediators have only rarely been studied in the alveolar compartment in patients with COVID-19 acute respiratory distress syndrome (CARDS) but have not been compared across different ARDS etiologies, and the potential effect of dexamethasone (DXM) on these mediators is not known. Methods: We assessed the integrity of the alveolo-capillary membrane, interleukins, type I, II, and III IFNs, and IFN autoantibodies by studying the epithelial lining fluid (ELF) volumes, alveolar concentration of protein, and ELF-corrected concentrations of cytokines in two patient subgroups and controls. Results: A total of 16 patients with CARDS (four without and 12 with DXM treatment), eight with non-CARDS, and 15 healthy controls were included. The highest ELF volumes and protein levels were observed in CARDS. Systemic and ELF-corrected alveolar concentrations of interleukin (IL)-6 appeared to be particularly low in patients with CARDS receiving DXM, whereas alveolar levels of IL-8 were high regardless of DXM treatment. Alveolar levels of IFNs were similar between CARDS and non-CARDS patients, and IFNα and IFNω autoantibody levels were higher in patients with CARDS and non-CARDS than in healthy controls. Conclusions: Patients with CARDS exhibited greater alveolo-capillary barrier disruption with compartmentalization of IL-8, regardless of DXM treatment, whereas systemic and alveolar levels of IL-6 were lower in the DXM-treated subgroup. IFN-I autoantibodies were higher in the BALF of CARDS patients, independent of DXM, whereas IFN autoantibodies in plasma were similar to those in controls.",
keywords = "acute respiratory distress syndrome, autoantibodies, bronchoalveolar lavage fluid, coronavirus disease 2019, inflammation, interferons",
author = "Jonassen, {Trine B.} and J{\o}rgensen, {Sofie E.} and Mitchell, {Nikki H.} and Mogensen, {Trine H.} and Berg, {Ronan M. G.} and Andreas Ronit and Plovsing, {Ronni R.}",
note = "Publisher Copyright: Copyright {\textcopyright} 2024 Jonassen, J{\o}rgensen, Mitchell, Mogensen, Berg, Ronit and Plovsing.",
year = "2024",
doi = "10.3389/fimmu.2024.1353012",
language = "English",
volume = "15",
journal = "Frontiers in Immunology",
issn = "1664-3224",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Alveolar cytokines and interferon autoantibodies in COVID-19 ARDS

AU - Jonassen, Trine B.

AU - Jørgensen, Sofie E.

AU - Mitchell, Nikki H.

AU - Mogensen, Trine H.

AU - Berg, Ronan M. G.

AU - Ronit, Andreas

AU - Plovsing, Ronni R.

N1 - Publisher Copyright: Copyright © 2024 Jonassen, Jørgensen, Mitchell, Mogensen, Berg, Ronit and Plovsing.

PY - 2024

Y1 - 2024

N2 - Background: Type I interferon (IFN-I) and IFN autoantibodies play a crucial role in controlling SARS-CoV-2 infection. The levels of these mediators have only rarely been studied in the alveolar compartment in patients with COVID-19 acute respiratory distress syndrome (CARDS) but have not been compared across different ARDS etiologies, and the potential effect of dexamethasone (DXM) on these mediators is not known. Methods: We assessed the integrity of the alveolo-capillary membrane, interleukins, type I, II, and III IFNs, and IFN autoantibodies by studying the epithelial lining fluid (ELF) volumes, alveolar concentration of protein, and ELF-corrected concentrations of cytokines in two patient subgroups and controls. Results: A total of 16 patients with CARDS (four without and 12 with DXM treatment), eight with non-CARDS, and 15 healthy controls were included. The highest ELF volumes and protein levels were observed in CARDS. Systemic and ELF-corrected alveolar concentrations of interleukin (IL)-6 appeared to be particularly low in patients with CARDS receiving DXM, whereas alveolar levels of IL-8 were high regardless of DXM treatment. Alveolar levels of IFNs were similar between CARDS and non-CARDS patients, and IFNα and IFNω autoantibody levels were higher in patients with CARDS and non-CARDS than in healthy controls. Conclusions: Patients with CARDS exhibited greater alveolo-capillary barrier disruption with compartmentalization of IL-8, regardless of DXM treatment, whereas systemic and alveolar levels of IL-6 were lower in the DXM-treated subgroup. IFN-I autoantibodies were higher in the BALF of CARDS patients, independent of DXM, whereas IFN autoantibodies in plasma were similar to those in controls.

AB - Background: Type I interferon (IFN-I) and IFN autoantibodies play a crucial role in controlling SARS-CoV-2 infection. The levels of these mediators have only rarely been studied in the alveolar compartment in patients with COVID-19 acute respiratory distress syndrome (CARDS) but have not been compared across different ARDS etiologies, and the potential effect of dexamethasone (DXM) on these mediators is not known. Methods: We assessed the integrity of the alveolo-capillary membrane, interleukins, type I, II, and III IFNs, and IFN autoantibodies by studying the epithelial lining fluid (ELF) volumes, alveolar concentration of protein, and ELF-corrected concentrations of cytokines in two patient subgroups and controls. Results: A total of 16 patients with CARDS (four without and 12 with DXM treatment), eight with non-CARDS, and 15 healthy controls were included. The highest ELF volumes and protein levels were observed in CARDS. Systemic and ELF-corrected alveolar concentrations of interleukin (IL)-6 appeared to be particularly low in patients with CARDS receiving DXM, whereas alveolar levels of IL-8 were high regardless of DXM treatment. Alveolar levels of IFNs were similar between CARDS and non-CARDS patients, and IFNα and IFNω autoantibody levels were higher in patients with CARDS and non-CARDS than in healthy controls. Conclusions: Patients with CARDS exhibited greater alveolo-capillary barrier disruption with compartmentalization of IL-8, regardless of DXM treatment, whereas systemic and alveolar levels of IL-6 were lower in the DXM-treated subgroup. IFN-I autoantibodies were higher in the BALF of CARDS patients, independent of DXM, whereas IFN autoantibodies in plasma were similar to those in controls.

KW - acute respiratory distress syndrome

KW - autoantibodies

KW - bronchoalveolar lavage fluid

KW - coronavirus disease 2019

KW - inflammation

KW - interferons

U2 - 10.3389/fimmu.2024.1353012

DO - 10.3389/fimmu.2024.1353012

M3 - Journal article

C2 - 38571960

AN - SCOPUS:85189170157

VL - 15

JO - Frontiers in Immunology

JF - Frontiers in Immunology

SN - 1664-3224

M1 - 1353012

ER -

ID: 388016102