Plasma IL-6 levels following corticosteroid therapy as an indicator of ICU length of stay in critically ill COVID-19 patients

Intensive care unit (ICU) admissions and mortality in severe COVID-19 patients are driven by “cytokine storms” and acute respiratory distress syndrome (ARDS). Interim clinical trial results suggest that the corticosteroid dexamethasone displays better 28-day survival in severe COVID-19 patients requ...

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Veröffentlicht in:Cell death discovery 2021-03, Vol.7 (1), p.55-55, Article 55
Hauptverfasser: Awasthi, Samir, Wagner, Tyler, Venkatakrishnan, A. J., Puranik, Arjun, Hurchik, Matthew, Agarwal, Vineet, Conrad, Ian, Kirkup, Christian, Arunachalam, Raman, O’Horo, John, Kremers, Walter, Kashyap, Rahul, Morice, William, Halamka, John, Williams, Amy W., Faubion, William A., Badley, Andrew D., Gores, Gregory J., Soundararajan, Venky
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Sprache:eng
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Zusammenfassung:Intensive care unit (ICU) admissions and mortality in severe COVID-19 patients are driven by “cytokine storms” and acute respiratory distress syndrome (ARDS). Interim clinical trial results suggest that the corticosteroid dexamethasone displays better 28-day survival in severe COVID-19 patients requiring ventilation or oxygen. In this study, 10 out of 16 patients (62.5%) that had an average plasma IL-6 value over 10 pg/mL post administration of corticosteroids also had worse outcomes (i.e., ICU stay >15 days or death), compared to 8 out of 41 patients (19.5%) who did not receive corticosteroids ( p -value = 0.0024). Given this potential association between post-corticosteroid IL-6 levels and COVID-19 severity, we hypothesized that the glucocorticoid receptor (GR or NR3C1) may be coupled to IL-6 expression in specific cell types that govern cytokine release syndrome (CRS). Examining single-cell RNA-seq data from BALF of severe COVID-19 patients and nearly 2 million cells from a pan-tissue scan shows that alveolar macrophages, smooth muscle cells, and endothelial cells co-express NR3C1 and IL-6, motivating future studies on the links between the regulation of NR3C1 function and IL-6 levels.
ISSN:2058-7716
2058-7716
DOI:10.1038/s41420-021-00429-9