Evidence map›Paper›PMID 30135596›Full record

ArticlePediatric research2018

LPS-induced maternal inflammation promotes fetal leukocyte recruitment and prenatal organ infiltration in mice.

Hannes Hudalla, Katinka Karenberg, Ruben-Jeremias Kuon, Johannes Pöschl, Raphaela Tschada, David Frommhold

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Pediatric research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The role of neutrophils in chorioamnionitis.Frontiers in immunology · 2023
    Review
  18. Article
  19. Review
  20. 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

6 authors at 3 institutions in 2 countries.

Hannes HudallaDepartment of Neonatology, Heidelberg University Children's Hospital, 69120, Heidelberg, Germany.
Katinka KarenbergDepartment of Neonatology, Heidelberg University Children's Hospital, 69120, Heidelberg, Germany.
Ruben-Jeremias KuonDepartment of Gynecological Endocrinology and Fertility Disorders, Heidelberg University Hospital, 69120, Heidelberg, Germany.
Johannes PöschlDepartment of Neonatology, Heidelberg University Children's Hospital, 69120, Heidelberg, Germany.
Raphaela TschadaDepartment of Neonatology, Heidelberg University Children's Hospital, 69120, Heidelberg, Germany.
David FrommholdDepartment of Neonatology, Heidelberg University Children's Hospital, 69120, Heidelberg, Germany. David.Frommhold@med.uni-heidelberg.de.
University Hospital Heidelberg · DEHeidelberg University · DEBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA pro-inflammatory intrauterine milieu accounts for increased perinatal morbidity and mortality. We asked how maternal inflammation as seen in endotoxemia affects fetal leukocyte recruitment in vivo during late gestation.

methodsInflammation was induced in pregnant LysEGFP-mice by intraperitoneal LPS injection between gestational day 14 and 18 (E14-E18). After 20 h, intravital fluorescence microscopy was performed on fetal yolk sac venules to examine leukocyte rolling (number of rolling cells/min) and adhesion (>30 s). Infiltration of neutrophils into chorion/amnion, lung, and kidney were quantified by immunofluorescence microscopy.

resultsAt high doses (2 × 1 mg/kg), LPS triggered preterm birth (PTB) and intrauterine fetal death (IUFD), with early gestations at high risk of IUFD and late gestations prone to PTB. Lower LPS dosing (2 × 0.25 mg/kg) did not induce labor, but promoted maternal and fetal cytokine production, as well as neutrophilic infiltration of fetal membranes, as seen in chorioamnionitis (CAM). Baseline fetal leukocyte recruitment increased throughout gestation, and maternal inflammation further augmented adhesion at E16-E18. Enhanced leukocyte recruitment ultimately translated into prominent infiltration of fetal lung and kidney.

conclusionLPS-induced maternal endotoxemia promotes IUFD, PTB, and fetal leukocyte recruitment depending on gestational age. Our proposed model may serve as a platform to test novel perinatal immune modulators.

Indexed as

AmnionAnimalsChorionFemaleFetusGreen Fluorescent ProteinsInflammationLeukocytesLipopolysaccharidesMaleMaternal-Fetal ExchangeMiceMice, Inbred C57BLPregnancyenhanced green fluorescent proteinGreen Fluorescent ProteinsLipopolysaccharides

Identifiers

PMID30135596
OpenAlexW2888422444

What OpenQuestion holds

Textmetadata
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.