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A distinct dexamethasone-dependent gene expression profile in the lungs of COVID-19 patients.
Fahnøe, Ulrik; Ronit, Andreas; Berg, Ronan M G; Jørgensen, Sofie E; Mogensen, Trine H; Underwood, Alexander P; Scheel, Troels K H; Bukh, Jens; Plovsing, Ronni R.
  • Fahnøe U; Copenhagen Hepatitis C Program (CO-HEP), Department of Infectious Diseases, Hvidovre Hospital and Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Ronit A; Department of Infectious Diseases, Copenhagen University Hospital - Amager and Hvidovre Hospitals, Hvidovre, Denmark.
  • Berg RMG; Department of Infectious Diseases, Copenhagen University Hospital - Amager and Hvidovre Hospitals, Hvidovre, Denmark.
  • Jørgensen SE; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Mogensen TH; Department of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
  • Underwood AP; Centre for Physical Activity Research, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
  • Scheel TKH; Neurovascular Research Laboratory, Faculty of Life Sciences and Education, University of South Wales, UK.
  • Bukh J; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Plovsing RR; Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
J Infect Dis ; 2022 May 27.
Article in English | MEDLINE | ID: covidwho-1873928
ABSTRACT
The effects of dexamethasone (DXM) treatment on pulmonary immunity in COVID-19 associated acute respiratory distress syndrome (CARDS) remain insufficiently understood. We performed transcriptomic RNA-seq analysis of bronchoalveolar lavage fluid from 20 mechanically ventilated patients 12 with CARDS (DXM+ or DXM-) and 8 non-COVID-19 critically ill controls. CARDS (+DXM) was characterized by upregulation of genes related to B-cell and complement pathway activation, antigen presentation, phagocytosis and FC-gamma receptor signalling. Most ISGs were upregulated in CARDS, particularly in CARDS (-DXM). In conclusion, DXM treatment was not associated with regulation of pro-inflammatory pathways in CARDS but with regulation of other local immune responses.
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Full text: Available Collection: International databases Database: MEDLINE Language: English Year: 2022 Document Type: Article Affiliation country: Infdis

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Full text: Available Collection: International databases Database: MEDLINE Language: English Year: 2022 Document Type: Article Affiliation country: Infdis