Evidence map›Paper›PMID 33277388›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2021

Cutting Edge: Severe SARS-CoV-2 Infection in Humans Is Defined by a Shift in the Serum Lipidome, Resulting in Dysregulation of Eicosanoid Immune Mediators.

Benjamin Schwarz, Lokesh Sharma, Lydia Roberts, Xiaohua Peng, Santos Bermejo, Ian Leighton, Arnau Casanovas-Massana, Maksym Minasyan, Shelli Farhadian, Albert I Ko and 3 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed, 1 pooled it
19.0field-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.

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

129 citing papers in PubMed, 1 synthesis or guideline pooled it, 204 citations in OpenAlex.

  1. Pooled it
  2. High levels of eicosanoids and docosanoids in the lungs of intubated COVID-19 patients.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Trial
  3. Article
  4. Article
  5. Heterogeneous Causes of Acute Respiratory Distress Syndrome Correlate With Distinct Peripheral Polyunsaturated Fatty Acid Metabolites.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Enhanced Production of Lipid Mediators in Plasma and Activation of DNA Damage Pathways in PBMCs Are Correlated With the Severity of Ancestral SARS-CoV-2 Infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Benjamin SchwarzLaboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840.
Lokesh SharmaSection of Pulmonary and Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, CT 06520.
Lydia RobertsLaboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840.
Xiaohua PengSection of Pulmonary and Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, CT 06520.ORCID 0000-0002-2973-2390
Santos BermejoSection of Pulmonary and Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, CT 06520.ORCID 0000-0003-0078-1989
Ian LeightonLaboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840.
Arnau Casanovas-MassanaDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT 06520; and.ORCID 0000-0002-3301-6143
Maksym MinasyanSection of Pulmonary and Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, CT 06520.
Shelli FarhadianSection of Infectious Diseases, Department of Medicine, Yale University School of Medicine, New Haven, CT 06520.
Albert I KoDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT 06520; and.ORCID 0000-0001-9023-2339
Yale IMPACT Team
Charles S Dela CruzSection of Pulmonary and Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, CT 06520; charles.delacruz@yale.edu bosioc@niaid.nih.gov.ORCID 0000-0002-5258-1797
Catharine M BosioLaboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840; charles.delacruz@yale.edu bosioc@niaid.nih.gov.
Yale University · USNational Institutes of Health · USNational Institute of Allergy and Infectious Diseases · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Systems investigation of vaccine responses in B cell depleted autoimmune patientsU19AI089992 · NIAID · YALE UNIVERSITY · PI David A. Hafler, RUTH R MONTGOMERY · 2010 to 2026
$50.4M
Effect of SARS-CoV-2 on host metabolism and its influence on innate and adaptive immunityZIAAI001281 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BOSIO, CATHARINE · 2020 to 2025
$1.1M
MAVS-Mediated Pulmonary Inflammation and Injury Response During Cigarette Smoke Exposure and Influenza Viral Infection and in COPDI01BX004661 · VA · VA CONNECTICUT HEALTHCARE SYSTEM · PI DELA CRUZ, CHARLES S · 2020 to 2024
–
BLRD VA I01 BX004661Intramural NIH HHS ZIA AI001281NCATS NIH HHS UL1 TR001863NIAID NIH HHS U19 AI089992
6 · The paper itself

Abstract

The COVID-19 pandemic has affected more than 20 million people worldwide, with mortality exceeding 800,000 patients. Risk factors associated with severe disease and mortality include advanced age, hypertension, diabetes, and obesity. Each of these risk factors pathologically disrupts the lipidome, including immunomodulatory eicosanoid and docosanoid lipid mediators (LMs). We hypothesized that dysregulation of LMs may be a defining feature of the severity of COVID-19. By examining LMs and polyunsaturated fatty acid precursor lipids in serum from hospitalized COVID-19 patients, we demonstrate that moderate and severe disease are separated by specific differences in abundance of immune-regulatory and proinflammatory LMs. This difference in LM balance corresponded with decreased LM products of ALOX12 and COX2 and an increase LMs products of ALOX5 and cytochrome p450. Given the important immune-regulatory role of LMs, these data provide mechanistic insight into an immuno-lipidomic imbalance in severe COVID-19.

Indexed as

COVID-19EicosanoidsLipidomicsSARS-CoV-2AdultAgedAged, 80 and overArachidonate 12-LipoxygenaseArachidonate 5-LipoxygenaseBiomarkersCyclooxygenase 2FemaleHumansMaleMiddle AgedALOX12 protein, humanALOX5 protein, humanArachidonate 12-LipoxygenaseArachidonate 5-LipoxygenaseBiomarkersCyclooxygenase 2EicosanoidsPTGS2 protein, human

Identifiers

PMID33277388
PMCPMC7962598
OpenAlexW3107123625

What OpenQuestion holds

Textmetadata
LicenceTDM
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.