Evidence map›Paper›PMID 39810405›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2025

The influence of interleukin-27 on metabolic fitness in a murine neonatal model of bacterial sepsis.

Jessica M Povroznik, Lei Wang, Madhavi Annamanedi, Rachael L Bare, Halima Akhter, Gangqing Hu, Cory M Robinson

Abstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

7 authors.

Jessica M PovroznikDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Lei WangDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Madhavi AnnamanediDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Rachael L BareDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Halima AkhterDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Gangqing HuDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.ORCID 0000-0001-5453-6888
Cory M RobinsonDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.ORCID 0000-0002-2122-2046

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI GARY O RANKIN · 2012 to 2026
$61.1M
Elucidating the mechanisms and consequences of MDSC-regulated immunity in TBR01AI164970 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Bryan David Bryson, Joshua T. Mattila · 2022 to 2026
$2.7M
Understanding IL-27 as a negative regulator of protective immunity during neonatal sepsisR01AI163333 · NIAID · WEST VIRGINIA UNIVERSITY · PI ROBINSON, CORY MICHAEL · 2021 to 2025
$2.4M
The regulation of early life interleukin-27 expression and metabolic impactR03AI154129 · NIAID · WEST VIRGINIA UNIVERSITY · PI ROBINSON, CORY MICHAEL · 2020 to 2021
$152k
HHS | National Institutes of Health (NIH) AI154129HHS | National Institutes of Health (NIH) AI163333NIAID NIH HHS R01 AI163333NIAID NIH HHS R01 AI164970NIAID NIH HHS R03 AI154129NIGMS NIH HHS P20 GM103434NIGMS NIH HHS U54 GM104942
6 · The paper itself

Abstract

Human neonates are predisposed to an increased risk of mortality from infection due to fundamental differences in the framework of innate and adaptive immune responses relative to those in the adult population. As one key difference in neonates, an increase in the immunosuppressive cytokine, IL-27, is responsible for poor outcomes in a murine neonatal model of bacterial sepsis. In our model, the absence of IL-27 signaling during infection is associated with improved maintenance of body mass, increased bacterial clearance with reduced systemic inflammation, and decreased mortality rates that correlate to preservation of glucose homeostasis and insulin production. To further elucidate the mechanisms associated with IL-27 signaling and metabolic fitness, we analyzed global transcriptomes from spleen, liver, pancreas, and hindlimb muscle during

Indexed as

Escherichia coli InfectionsInterleukin-27InterleukinsNeonatal SepsisSepsisAnimalsAnimals, NewbornDisease Models, AnimalEscherichia coliGluconeogenesisLipid MetabolismLiverMiceMice, Inbred C57BLMice, KnockoutMuscle, SkeletalIl27 protein, mouseIl27ra protein, mouseInterleukin-27InterleukinsReceptors, Interleukingluconeogenesisglycolysisinterleukin-27metabolismneonatal sepsis

Identifiers

PMID39810405
PMCPMC12184839

What OpenQuestion holds

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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.