Evidence map›Paper›PMID 36779805›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

IL-1/MyD88-Dependent G-CSF and IL-6 Secretion Mediates Postburn Anemia.

John G Noel, Seth W Ramser, Lori Pitstick, Holly S Goetzman, Elizabeth L Dale, Andrew Potter, Mike Adam, S Steven Potter, Jason C Gardner

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors at 3 institutions in 1 country.

John G NoelDivision of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati College of Medicine, Cincinnati, OH.
Seth W RamserDivision of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati College of Medicine, Cincinnati, OH.
Lori PitstickDivision of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati College of Medicine, Cincinnati, OH.
Holly S GoetzmanDivision of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati College of Medicine, Cincinnati, OH.
Elizabeth L DaleDepartment of Surgery, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0002-3644-1591
Andrew PotterDevelopmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Mike AdamDevelopmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.ORCID 0000-0003-4501-4740
S Steven PotterDevelopmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Jason C GardnerDivision of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati College of Medicine, Cincinnati, OH.
University of Cincinnati · USCincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · US

Funding

Inflammatory Mechanisms in Post Burn Anemia of Critical IllnessR01HL155579 · NHLBI · UNIVERSITY OF CINCINNATI · PI Jason Gardner · 2022 to 2026
$2.1M
NHLBI NIH HHS R01 HL155579
6 · The paper itself

Abstract

The anemia of critical illness (ACI) is a nearly universal pathophysiological consequence of burn injury and a primary reason burn patients require massive quantities of transfused blood. Inflammatory processes are expected to drive postburn ACI and prevent meaningful erythropoietic stimulation through iron or erythropoietin supplementation, but to this day no specific inflammatory pathways have been identified as a critical mechanism. In this study, we examined whether secretion of G-CSF and IL-6 mediates distinct features of postburn ACI and interrogated inflammatory mechanisms that could be responsible for their secretion. Our analysis of mouse and human skin samples identified the burn wound as a primary source of G-CSF and IL-6 secretion. We show that G-CSF and IL-6 are secreted independently through an IL-1/MyD88-dependent mechanism, and we ruled out TLR2 and TLR4 as critical receptors. Our results indicate that IL-1/MyD88-dependent G-CSF secretion plays a key role in impairing medullary erythropoiesis and IL-6 secretion plays a key role in limiting the access of erythroid cells to iron. Importantly, we found that IL-1α/β neutralizing Abs broadly attenuated features of postburn ACI that could be attributed to G-CSF or IL-6 secretion and rescued deficits of circulating RBC counts, hemoglobin, and hematocrit caused by burn injury. We conclude that wound-based IL-1/MyD88 signaling mediates postburn ACI through induction of G-CSF and IL-6 secretion.

Indexed as

AnemiaBurnsGranulocyte Colony-Stimulating FactorHumansInterleukin-1Interleukin-6IronMyeloid Differentiation Factor 88Granulocyte Colony-Stimulating FactorInterleukin-1Interleukin-6IronMyeloid Differentiation Factor 88

Identifiers

PMID36779805
PMCPMC10038902
OpenAlexW4320485538

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.