Evidence map›Paper›PMID 35081105›Full record

ArticlePloS one2022

RNA Sequencing in COVID-19 patients identifies neutrophil activation biomarkers as a promising diagnostic platform for infections.

Richard Wargodsky, Philip Dela Cruz, John LaFleur, David Yamane, Justin Sungmin Kim, Ivy Benjenk, Eric Heinz, Obinna Ome Irondi, Katherine Farrar, Ian Toma and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Richard WargodskyDepartment of Medicine, Division of Genomic Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
Philip Dela CruzDepartment Anesthesiology and Critical Care Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
John LaFleurDepartment of Emergency Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
David YamaneDepartment Anesthesiology and Critical Care Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
Justin Sungmin KimDepartment Anesthesiology and Critical Care Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
Ivy BenjenkDepartment Anesthesiology and Critical Care Medicine, The George Washington University Medical Center, Washington, DC, United States of America.ORCID 0000-0002-5057-9300
Eric HeinzDepartment Anesthesiology and Critical Care Medicine, The George Washington University Medical Center, Washington, DC, United States of America.ORCID 0000-0002-3194-8553
Obinna Ome IrondiDepartment Anesthesiology and Critical Care Medicine, The George Washington University Medical Center, Washington, DC, United States of America.ORCID 0000-0001-5453-9456
Katherine FarrarDepartment Anesthesiology and Critical Care Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
Ian TomaDepartment of Medicine, Division of Genomic Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
Tristan JordanDepartment of Medicine, Division of Genomic Medicine, The George Washington University Medical Center, Washington, DC, United States of America.ORCID 0000-0003-0943-5935
Jennifer GoldmanDepartment of Medicine, Division of Genomic Medicine, The George Washington University Medical Center, Washington, DC, United States of America.
Timothy A McCaffreyDepartment of Medicine, Division of Genomic Medicine, The George Washington University Medical Center, Washington, DC, United States of America.ORCID 0000-0002-4648-7833
George Washington University · US

Funding

Clinical and Translational Science Institute at Childrens NationalUL1TR001876 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI BELL, MICHAEL J · 2016 to 2021
$25.6M
Acquisition of the BioRad QX200 AutoDG Droplet Digital PCR SystemS10OD021622 · OD · GEORGE WASHINGTON UNIVERSITY · PI JONES, R. BRAD · 2016 to 2016
$125k
NCATS NIH HHS UL1 TR001876NIH HHS S10 OD021622
6 · The paper itself

Abstract

Infection with the SARS-CoV2 virus can vary from asymptomatic, or flu-like with moderate disease, up to critically severe. Severe disease, termed COVID-19, involves acute respiratory deterioration that is frequently fatal. To understand the highly variable presentation, and identify biomarkers for disease severity, blood RNA from COVID-19 patient in an intensive care unit was analyzed by whole transcriptome RNA sequencing. Both SARS-CoV2 infection and the severity of COVID-19 syndrome were associated with up to 25-fold increased expression of neutrophil-related transcripts, such as neutrophil defensin 1 (DEFA1), and 3-5-fold reductions in T cell related transcripts such as the T cell receptor (TCR). The DEFA1 RNA level detected SARS-CoV2 viremia with 95.5% sensitivity, when viremia was measured by ddPCR of whole blood RNA. Purified CD15+ neutrophils from COVID-19 patients were increased in abundance and showed striking increases in nuclear DNA staining by DAPI. Concurrently, they showed >10-fold higher elastase activity than normal controls, and correcting for their increased abundance, still showed 5-fold higher elastase activity per cell. Despite higher CD15+ neutrophil elastase activity, elastase activity was extremely low in plasma from the same patients. Collectively, the data supports the model that increased neutrophil and decreased T cell activity is associated with increased COVID-19 severity, and suggests that blood DEFA1 RNA levels and neutrophil elastase activity, both involved in neutrophil extracellular traps (NETs), may be informative biomarkers of host immune activity after viral infection.

Indexed as

Adultalpha-DefensinsBiomarkersCOVID-19FemaleHumansIntensive Care UnitsLewis X AntigenMaleMiddle AgedNeutrophil ActivationNeutrophilsPancreatic ElastaseReceptors, Antigen, T-CellRNA, ViralSARS-CoV-2alpha-DefensinsBiomarkershuman neutrophil peptide 1Lewis X AntigenPancreatic ElastaseReceptors, Antigen, T-CellRNA, Viral

Identifiers

PMID35081105
PMCPMC8791486
OpenAlexW4210354992

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.