Evidence map›Paper›PMID 25589517›Full record

ArticleMolecular human reproduction2015

Activation of decidual invariant natural killer T cells promotes lipopolysaccharide-induced preterm birth.

Liping Li, Jing Yang, Yao Jiang, Jiaoqin Tu, Danny J Schust

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Molecular human reproduction, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. The landscape of decidual immune cells at the maternal-fetal interface in parturition and preterm birth.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. IL-27 Mediates Pro-Inflammatory EffectsFrontiers in immunology · 2021
    Article
  8. Review
  9. Article
  10. Immunobiology of Acute Chorioamnionitis.Frontiers in immunology · 2020
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Mapping out p38MAPK.American journal of reproductive immunology (New York, N.Y. : 1989) · 2017
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 2 countries.

Liping LiDepartment of Obstetrics and Gynecology, Guangzhou Medical University Affiliated Guangzhou First People's Hospital, Guangzhou 510180, China.
Jing YangDepartment of Obstetrics and Gynecology, Guangzhou Medical University Affiliated Guangzhou First People's Hospital, Guangzhou 510180, China.
Yao JiangDepartment of Obstetrics and Gynecology, Guangzhou Medical University Affiliated Guangzhou First People's Hospital, Guangzhou 510180, China.
Jiaoqin TuDepartment of Obstetrics and Gynecology, Guangzhou Medical University Affiliated Guangzhou First People's Hospital, Guangzhou 510180, China.
Danny J SchustDepartment of Obstetrics, Gynecology and Women's Health, University of Missouri School of Medicine, Columbia, MO 65201, USA schustd@health.missouri.edu.
First Affiliated Hospital of Guangzhou Medical University · CNGuangzhou First People's Hospital · CNGuangzhou Medical University · CNUniversity of Missouri Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells are crucial for host defense against a variety of microbial pathogens, but the underlying mechanisms of iNKT cells activation by microbes are not fully explained. In this study, we investigated the molecular mechanisms of iNKT cell activation in lipopolysaccharide (LPS)-stimulated preterm birth using an adoptive transfer system and diverse neutralizing antibodies (Abs) and inhibitors. We found that adoptive transfer of decidual iNKT cells to LPS-stimulated iNKT cell deficient Jα18(-/-) mice that lack invariant Vα14Jα281T cell receptor (TCR) expression significantly decreased the time to delivery and increased the percentage of decidual iNKT cells. Neutralizing Abs against Toll-like receptor 4 (TLR-4), CD1d, interleukin (IL)-12 and IL-18, and inhibitors blocking the activation of nuclear factor κB (NF-κB), mitogen-activated protein kinase (MAPK) p38 and extracellular signal-regulated kinase (ERK) significantly reduced in vivo percentages of decidual iNKT cells, their intracellular interferon (IFN)-γ production and surface CD69 expression. In vitro, in the presence of the same Abs and inhibitors used as in vivo, decidual iNKT cells co-cultured with LPS-pulsed dendritic cells (DCs) showed significantly decreased extracellular and intracellular IFN-γ secretion and surface CD69 expression. Our data demonstrate that the activation of decidual iNKT cells plays an important role in inflammation-induced preterm birth. Activation of decidual iNKT cells also requires TLR4-mediated NF-κB, MAPK p38 and ERK pathways, the proinflammatory cytokines IL-12 and IL-18, and endogenous glycolipid antigens presented by CD1d.

Indexed as

Adoptive TransferAnimalsAntibodies, NeutralizingAntigens, CDAntigens, CD1dAntigens, Differentiation, T-LymphocyteCD69 AntigensCoculture TechniquesDeciduaDendritic CellsExtracellular Signal-Regulated MAP KinasesFemaleGene Expression RegulationInterferon-gammaInterleukin-12Interleukin-18Antibodies, NeutralizingAntigens, CDAntigens, CD1dAntigens, Differentiation, T-LymphocyteCD1d antigen, mouseCD69 AntigensExtracellular Signal-Regulated MAP KinasesInterferon-gammaInterleukin-12Interleukin-18Lectins, C-TypeLipopolysaccharidesNF-kappa Bp38 Mitogen-Activated Protein KinasesReceptors, Antigen, T-CellTlr4 protein, mouseToll-Like Receptor 4activationinflammationlipopolysaccharidenatural killer T cellspreterm birth

Identifiers

PMID25589517
OpenAlexW2154877954

What OpenQuestion holds

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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.