Evidence map›Paper›PMID 36341409›Full record

ArticleFrontiers in immunology2022

Abrogation of neutrophil inflammatory pathways and potential reduction of neutrophil-related factors in COVID-19 by intravenous immunoglobulin.

Jorge Adrian Masso-Silva, George Sakoulas, Jarod Olay, Victoria Groysberg, Matthew Geriak, Victor Nizet, Laura E Crotty Alexander, Angela Meier

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
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

8 authors at 5 institutions in 1 country.

Jorge Adrian Masso-SilvaSection of Pulmonary and Critical Care, Veterans Affairs (VA) San Diego, La Jolla, CA, United States.
George SakoulasDepartment of Infectious Disease, Sharp Rees-Stealy Medical Group, San Diego, CA, United States.
Jarod OlaySection of Pulmonary and Critical Care, Veterans Affairs (VA) San Diego, La Jolla, CA, United States.
Victoria GroysbergDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California (UC) San Diego, La Jolla, CA, United States.
Matthew GeriakDepartment of Research, Sharp Healthcare, San Diego, CA, United States.
Victor NizetDivision of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California (UC) San Diego, La Jolla, CA, United States.
Laura E Crotty AlexanderSection of Pulmonary and Critical Care, Veterans Affairs (VA) San Diego, La Jolla, CA, United States.
Angela MeierDepartment of Anesthesiology, Division of Critical Care, UCSD, La Jolla, CA, United States.
University of California, San Diego · USSan Francisco VA Medical Center · USSharp HealthCare Foundation · USSharp Rees-Stealy Medical Group · USUniversity of Montana · US

Funding

UC San Diego Clinical and Translational Research InstituteKL2TR001444 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEPP, COLIN A. · 2015 to 2024
$15.4M
Cathelicidin in Skin ImmunityR37AI052453 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Richard L Gallo, Victor Nizet · 2019 to 2026
$4.6M
Electronic Cigarette Vapor Inhalation Adversely Affects Lung Cellular and Physiologic Function and Alters Systemic Inflammatory PathwaysR01HL137052 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CROTTY ALEXANDER, LAURA ELISE · 2017 to 2021
$2.3M
Convergence of Vitamin E, THC, Nicotine, Propylene Glycol and Glycerin Effects on Lung Inflammation When VapedK24HL155884 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Laura Elise Crotty Alexander · 2022 to 2026
$609k
Hypoxia inducible factors in pulmonary endothelial cells regulate allergic inflammatory airways diseaseI01BX004767 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI CROTTY ALEXANDER, LAURA ELISE · 2020 to 2023
–
BLRD VA I01 BX004767NCATS NIH HHS KL2 TR001444NHLBI NIH HHS K24 HL155884NHLBI NIH HHS R01 HL137052NIAID NIH HHS R37 AI052453
6 · The paper itself

Abstract

Pathogenesis of lung injury in COVID-19 is not completely understood, leaving gaps in understanding how current treatments modulate the course of COVID-19. Neutrophil numbers and activation state in circulation have been found to correlate with COVID-19 severity, and neutrophil extracellular traps (NETs) have been found in the lung parenchyma of patients with acute respiratory distress syndrome (ARDS) in COVID-19. Targeting the pro-inflammatory functions of neutrophils may diminish lung injury in COVID-19 and ARDS. Neutrophils were isolated from peripheral blood of healthy donors, treated

Indexed as

Cell-Free Nucleic AcidsCOVID-19 Drug TreatmentLung InjuryRespiratory Distress SyndromeDexamethasoneHumansImmunoglobulins, IntravenousLeukocyte ElastaseNeutrophilsCell-Free Nucleic AcidsDexamethasoneImmunoglobulins, IntravenousLeukocyte ElastasecorticosteroidsCOVID-19dexamethasoneintravenous immunoglobulin (IVIG)NETosisneutrophilsoxidative bursttocilizumab

Identifiers

PMID36341409
PMCPMC9632428
OpenAlexW4306879646

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.