Evidence map›Paper›PMID 32302401›Full record

ArticleThe Journal of experimental medicine2020

Targeting potential drivers of COVID-19: Neutrophil extracellular traps.

Betsy J Barnes, Jose M Adrover, Amelia Baxter-Stoltzfus, Alain Borczuk, Jonathan Cools-Lartigue, James M Crawford, Juliane Daßler-Plenker, Philippe Guerci, Caroline Huynh, Jason S Knight and 13 more

3 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 965 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
965citing papers in PubMed, 4 pooled it
109.3field-weighted citation impact, top 1% 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.

NCT04387786 completednot on this map

Nebulized In-line Endotracheal Dornase Alfa and Albuterol Administered to Mechanically Ventilated COVID-19 Patients: A Case Series

TypeobservationalSponsorFeinstein Institute for Medical ResearchRan2020 to 2020Enrolled5ConditionsCOVID-19, Mechanical VentilationArmsDornase Alfa
NCT04402970 phase3completednot on this map

Inhaled Dornase Alfa for Treatment of ARDS in Patients With SARS-CoV-2

TypeinterventionalSponsorUniversity of Missouri-ColumbiaRan2020 to 2020Enrolled30ConditionsSARS-CoV 2, ARDSArmsDornase Alfa Inhalation Solution
NCT04540926 phase1 / phase2unknown statusnot on this map

Utility of Low Doses of Corticosteroids and Cyclosporine Combined With Enoxaparin, in Patients With COVID-19 Pneumonia at the ISSSTE Regional Hospital, Puebla, During the Contingency Period Due to the SARS-Cov2 Pandemic

TypeinterventionalSponsorInstituto de Seguridad y Servicios Sociales de los Trabajadores del EstadoRan2020 to 2020Enrolled200ConditionsCOVID 19 PneumoniaArmsCyclosporin A
3 · Its place in the literature

Who cites it

965 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,572 citations in OpenAlex.

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905 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 11 institutions in 3 countries.

Betsy J BarnesCenter for Autoimmune, Musculoskeletal and Hematopoietic Diseases, The Feinstein Institutes for Medical Research & Departments of Molecular Medicine and Pediatrics, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY.
Jose M AdroverCold Spring Harbor Laboratory, Cold Spring Harbor, NY.
Amelia Baxter-StoltzfusDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.
Alain BorczukDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.
Jonathan Cools-LartigueDivision of Thoracic and Upper GI Surgery, Department of Surgery, Montreal, Canada.
James M CrawfordDepartment of Pathology and Laboratory Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, East Garden City, NY.
Juliane Daßler-PlenkerCold Spring Harbor Laboratory, Cold Spring Harbor, NY.
Philippe GuerciCentre Hospitalier Universitaire de Nancy, Nancy, France.
Caroline HuynhDivision of Thoracic and Upper GI Surgery, Department of Surgery, Montreal, Canada.
Jason S KnightDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.
Massimo LodaDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.
Mark R LooneyDepartment of Medicine, University of California, San Francisco, San Francisco, CA.
Florencia McAllisterDepartment of Clinical Cancer Prevention, University of Texas MD Anderson Cancer Center, Houston, TX.
Roni RayesDivision of Thoracic and Upper GI Surgery, Department of Surgery, Montreal, Canada.
Stephane RenaudCentre Hospitalier Universitaire de Nancy, Nancy, France.
Simon RousseauDepartment of Medicine, McGill University & The Research Institute of the McGill University Health Centre, Montreal, Canada.
Steven SalvatoreDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY.
Robert E SchwartzDivision of Gastroenterology and Hepatology, Department of Medicine, Weill Cornell Medicine, New York, NY.
Jonathan D SpicerDivision of Thoracic and Upper GI Surgery, Department of Surgery, Montreal, Canada.
Christian C YostDepartment of Pediatrics, Program in Molecular Medicine, University of Utah School of Medicine, Salt Lake City, UT.
Andrew WeberDivision of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, Northwell Health, Manhasset, NY.
Yu ZuoDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.
Mikala EgebladCold Spring Harbor Laboratory, Cold Spring Harbor, NY.
Cornell University · USMcGill University Health Centre · CACold Spring Harbor Laboratory · USCentre Hospitalier Régional et Universitaire de Nancy · FRUniversity of Michigan · USDonald & Barbara Zucker School of Medicine at Hofstra/Northwell · USFeinstein Institute for Medical Research · USNorthwell Health · USThe University of Texas MD Anderson Cancer Center · USUniversity of California, San Francisco · USUniversity of Utah · US

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI LINGBO ZHANG · 1987 to 2026
$118.9M
Purinergic modulation of the autoimmune vascular phenotypeR01HL134846 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jason Knight · 2018 to 2026
$4.8M
IRF5 and Macrophage Activation Syndrome in systemic Juvenile Idiopathic ArthritisR01AR076242 · NIAMS · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI BARNES, BETSY J, HAMERMAN, JESSICA A · 2019 to 2023
$3.3M
Optimization of the engineered 3D hepatic microenvironment enhances pluripotent stem cell derived hepatocyteR01DK121072 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI SCHWARTZ, ROBERT E · 2020 to 2024
$2.6M
NETs: Protection or Harm in Neonatal Inflammation and InfectionR01HD093826 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI CHRISTIAN CON YOST · 2018 to 2026
$2.6M
Fine-tuning the Neutrophilic Response to PneumoniaR01AI125445 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2016 to 2020
$2.2M
Innate Immune Mechanisms of Primary Graft Dysfunction after Lung TransplantationR01HL130324 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2016 to 2019
$2.2M
Modeling Hepatoblastoma using pluripotent stem cell derived hepatocyte-like cellsR01CA234614 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI SCHWARTZ, ROBERT E · 2019 to 2023
$1.9M
NCI NIH HHS P30 CA045508NHLBI NIH HHS R01 HL130324NHLBI NIH HHS R01 HL134846NIAID NIH HHS R01 AI125445NIAMS NIH HHS R01 AR076242NICHD NIH HHS R01 HD093826NIDDK NIH HHS R01 DK121072
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) is a novel, viral-induced respiratory disease that in ∼10-15% of patients progresses to acute respiratory distress syndrome (ARDS) triggered by a cytokine storm. In this Perspective, autopsy results and literature are presented supporting the hypothesis that a little known yet powerful function of neutrophils-the ability to form neutrophil extracellular traps (NETs)-may contribute to organ damage and mortality in COVID-19. We show lung infiltration of neutrophils in an autopsy specimen from a patient who succumbed to COVID-19. We discuss prior reports linking aberrant NET formation to pulmonary diseases, thrombosis, mucous secretions in the airways, and cytokine production. If our hypothesis is correct, targeting NETs directly and/or indirectly with existing drugs may reduce the clinical severity of COVID-19.

Indexed as

BetacoronavirusExtracellular TrapsLung DiseasesCoronavirus InfectionsCOVID-19CytokinesHumansNeutrophilsPandemicsPneumonia, ViralSARS-CoV-2Cytokines

Identifiers

PMID32302401
PMCPMC7161085
OpenAlexW3016393661

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.