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


Journal

Cell death discovery
ISSN: 2058-7716
Titre abrégé: Cell Death Discov
Pays: United States
ID NLM: 101665035

Informations de publication

Date de publication:
15 Mar 2021
Historique:
received: 27 09 2020
accepted: 04 12 2020
revised: 14 11 2020
entrez: 16 3 2021
pubmed: 17 3 2021
medline: 17 3 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 33723251
doi: 10.1038/s41420-021-00429-9
pii: 10.1038/s41420-021-00429-9
pmc: PMC7958587
doi:

Types de publication

Journal Article

Langues

eng

Pagination

55

Subventions

Organisme : U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
ID : AI120698
Organisme : amfAR, The Foundation for AIDS Research (amfAR)
ID : 109593-62-RGRL

Références

Br J Pharmacol. 2011 May;163(1):29-43
pubmed: 21198556
Immunol Rev. 2017 Mar;276(1):5-8
pubmed: 28258698
Hematology Am Soc Hematol Educ Program. 2016 Dec 2;2016(1):366-378
pubmed: 27913503
Nat Rev Immunol. 2017 Apr;17(4):233-247
pubmed: 28192415
N Engl J Med. 2020 Jun 11;382(24):2372-2374
pubmed: 32302078
EClinicalMedicine. 2020 Jun 20;24:100418
pubmed: 32766537
Lancet. 2020 Feb 15;395(10223):473-475
pubmed: 32043983
Med Mal Infect. 2020 Jun;50(4):382-383
pubmed: 32259560
Infect Dis Poverty. 2020 Apr 28;9(1):45
pubmed: 32345362
Int J Oral Sci. 2020 Feb 24;12(1):8
pubmed: 32094336
Nat Med. 2020 Jun;26(6):842-844
pubmed: 32398875
Lancet. 2020 May 2;395(10234):1417-1418
pubmed: 32325026
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
Front Immunol. 2019 Aug 27;10:2028
pubmed: 31507614
N Engl J Med. 2020 Jul 9;383(2):120-128
pubmed: 32437596
N Engl J Med. 2020 Sep 3;383(10):994
pubmed: 32649078
Endocrinology. 2016 Nov;157(11):4257-4265
pubmed: 27649090
Lancet. 2020 May 16;395(10236):1569-1578
pubmed: 32423584
J Clin Invest. 1974 Dec;54(6):1337-43
pubmed: 4612058
N Engl J Med. 2020 Aug 6;383(6):517-525
pubmed: 32492293
Elife. 2020 Jul 07;9:
pubmed: 32633720
FASEB J. 2019 Dec;33(12):14067-14082
pubmed: 31657630
Cell. 2020 May 28;181(5):1016-1035.e19
pubmed: 32413319
Sci Rep. 2016 Mar 14;6:23002
pubmed: 26972611
Elife. 2020 May 28;9:
pubmed: 32463365
Eur J Immunol. 1990 Nov;20(11):2439-43
pubmed: 2253684
BMC Genet. 2019 Feb 8;20(1):16
pubmed: 30736733
N Engl J Med. 2020 Dec 10;383(24):2333-2344
pubmed: 33085857
Blood. 2012 Apr 12;119(15):3383-93
pubmed: 22323450
Nat Rev Immunol. 2020 Jul;20(7):389-391
pubmed: 32439870
Mol Cell Endocrinol. 2011 Mar 15;335(1):2-13
pubmed: 20398732
QJM. 2000 Feb;93(2):105-11
pubmed: 10700481
Proc Natl Acad Sci U S A. 2020 May 19;117(20):10970-10975
pubmed: 32350134
Lancet Rheumatol. 2020 Aug;2(8):e465-e473
pubmed: 32835256
Clin Exp Immunol. 1980 Apr;40(1):83-8
pubmed: 7389219

Auteurs

Samir Awasthi (S)

nference, Cambridge, MA, 02142, USA.

Tyler Wagner (T)

nference, Cambridge, MA, 02142, USA.

A J Venkatakrishnan (AJ)

nference, Cambridge, MA, 02142, USA.

Arjun Puranik (A)

nference, Cambridge, MA, 02142, USA.

Matthew Hurchik (M)

nference, Cambridge, MA, 02142, USA.

Vineet Agarwal (V)

nference, Cambridge, MA, 02142, USA.

Ian Conrad (I)

nference, Cambridge, MA, 02142, USA.

Christian Kirkup (C)

nference, Cambridge, MA, 02142, USA.

Raman Arunachalam (R)

nference Labs, Bangalore, India.

John O'Horo (J)

Mayo Clinic, Rochester, MN, 55905, USA.

Walter Kremers (W)

Mayo Clinic, Rochester, MN, 55905, USA.

Rahul Kashyap (R)

Mayo Clinic, Rochester, MN, 55905, USA.

William Morice (W)

Mayo Clinic, Rochester, MN, 55905, USA.
Mayo Clinic Laboratories, Rochester, MN, 55905, USA.

John Halamka (J)

Mayo Clinic, Rochester, MN, 55905, USA.
Mayo Clinic Platform, Rochester, MN, 55905, USA.

Amy W Williams (AW)

Mayo Clinic, Rochester, MN, 55905, USA.

William A Faubion (WA)

Mayo Clinic, Rochester, MN, 55905, USA.

Andrew D Badley (AD)

Mayo Clinic, Rochester, MN, 55905, USA.

Gregory J Gores (GJ)

Mayo Clinic, Rochester, MN, 55905, USA.

Venky Soundararajan (V)

nference, Cambridge, MA, 02142, USA. venky@nference.net.

Classifications MeSH