| Literature DB >> 33723251 |
Samir Awasthi1, Tyler Wagner1, A J Venkatakrishnan1, Arjun Puranik1, Matthew Hurchik1, Vineet Agarwal1, Ian Conrad1, Christian Kirkup1, Raman Arunachalam2, John O'Horo3, Walter Kremers3, Rahul Kashyap3, William Morice3,4, John Halamka3,5, Amy W Williams3, William A Faubion3, Andrew D Badley3, Gregory J Gores3, Venky Soundararajan6.
Abstract
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.Entities:
Year: 2021 PMID: 33723251 PMCID: PMC7958587 DOI: 10.1038/s41420-021-00429-9
Source DB: PubMed Journal: Cell Death Discov ISSN: 2058-7716