Evidence map›Paper›PMID 35906309›Full record

ArticlePediatric research2023

Decreased expression of hypoxia-inducible factor 1α (HIF-1α) in cord blood monocytes under anoxia.

Christiane Schlegel, Kai Liu, Bärbel Spring, Stefanie Dietz, Christian F Poets, Hannes Hudalla, Trim Lajqi, Natascha Köstlin-Gille, Christian Gille

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Article in Pediatric research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  5. HSPBiomedicines · 2025
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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 2 institutions in 1 country.

Christiane Schlegel *Department of Neonatology, Tübingen University Children's Hospital, Tübingen, Germany.
Kai Liu *Department of Neonatology, Tübingen University Children's Hospital, Tübingen, Germany.
Bärbel SpringDepartment of Neonatology, Tübingen University Children's Hospital, Tübingen, Germany.
Stefanie DietzDepartment of Neonatology, Tübingen University Children's Hospital, Tübingen, Germany.
Christian F PoetsDepartment of Neonatology, Tübingen University Children's Hospital, Tübingen, Germany.
Hannes HudallaDepartment of Neonatology, Heidelberg University Children's Hospital, Heidelberg, Germany.
Trim LajqiDepartment of Neonatology, Heidelberg University Children's Hospital, Heidelberg, Germany.
Natascha Köstlin-GilleDepartment of Neonatology, Tübingen University Children's Hospital, Tübingen, Germany. natascha.koestlin@med.uni-tuebingen.de.ORCID 0000-0003-3718-5507
Christian GilleDepartment of Neonatology, Heidelberg University Children's Hospital, Heidelberg, Germany.
Heidelberg University · DEUniversity Children's Hospital Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfections are a major cause for morbidity and mortality in neonates; however, the underling mechanisms for increased infection susceptibility are incompletely understood. Hypoxia, which is present in inflamed tissues, has been identified as an important activation signal for innate immune cells in adults and is mainly mediated by hypoxia-inducible factor 1α (HIF-1α). Fetal tissue pO

methodsIn this study, the effect of low oxygen partial pressure (pO

resultsWe show that anoxia-induced HIF-1α protein accumulation, phagocytosis, ROS-production and VEGF-expression were greatly diminished in cord blood compared to adult cells. E. coli led to HIF-1α gene expression in adult and cord blood immune cells; however, cord blood cells failed to accumulate HIF-1α protein and VEGF upon E. coli stimulation.

conclusionsTaken together, our results show a diminished activation of cord blood immune cells by low pO IMPACT: Neonatal immune cells do not accumulate HIF-1α under low oxygen partial pressure leading to decreased phagocytosis and decreased ROS production. We demonstrate a previously unknown mechanism of reduced activation of neonatal immune cells in the context of an inflammatory response. This could contribute to the increased susceptibility of newborns and preterm infants to infection.

Indexed as

Fetal BloodVascular Endothelial Growth Factor AAdultEscherichia coliHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitInfant, NewbornInfant, PrematureMonocytesOxygenReactive Oxygen SpeciesHypoxia-Inducible Factor 1, alpha SubunitOxygenReactive Oxygen SpeciesVascular Endothelial Growth Factor A

Identifiers

PMID35906309
PMCPMC10033401
OpenAlexW4288690057

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Textfull text, public
LicenceCC BY
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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.