Evidence map›Paper›PMID 26602702›Full record

ArticleTraffic (Copenhagen, Denmark)2016

Macrophage Exosomes Induce Placental Inflammatory Cytokines: A Novel Mode of Maternal-Placental Messaging.

Beth Holder, Tessa Jones, Vanessa Sancho Shimizu, Thomas F Rice, Beverly Donaldson, Marielle Bouqueau, Karen Forbes, Beate Kampmann

Open access · hybridAbstract read
In one paragraph

Article in Traffic (Copenhagen, Denmark), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Identifying Key Questions and Challenges in Microchimerism Biology.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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  7. Review
  8. Journal of dental research · 2025
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  9. Article
  10. Review
  11. The role of microRNAs in pregnancies complicated by maternal diabetes.Clinical science (London, England : 1979) · 2024
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review

20 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 2 countries.

Beth HolderSection of Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Tessa JonesSection of Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Vanessa Sancho ShimizuSection of Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Thomas F RiceSection of Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Beverly DonaldsonSection of Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Marielle BouqueauSection of Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Karen ForbesDivision of Reproduction and Early Development, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), The University of Leeds, Leeds, UK.
Beate KampmannSection of Paediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, UK.
Imperial College London · GBManchester Academic Health Science Centre · GB

Funding

Medical Research Council MC_UP_A900_1122MRF_ C0483
6 · The paper itself

Abstract

During pregnancy, the placenta forms the interface between mother and fetus. Highly controlled regulation of trans-placental trafficking is therefore essential for the healthy development of the growing fetus. Extracellular vesicle-mediated transfer of protein and nucleic acids from the human placenta into the maternal circulation is well documented; the possibility that this trafficking is bi-directional has not yet been explored but could affect placental function and impact on the fetus.We hypothesized that the ability of the placenta to respond to maternal inflammatory signals is mediated by the interaction of maternal immune cell exosomes with placental trophoblast. Utilizing the BeWo cell line and whole placental explants, we demonstrated that the human placenta internalizes macrophage-derived exosomes in a time- and dose-dependent manner. This uptake was via clathrin-dependent endocytosis. Furthermore, macrophage exosomes induced release of proinflammatory cytokines by the placenta. Taken together, our data demonstrates that exosomes are actively transported into the human placenta and that exosomes from activated immune cells modulate placental cytokine production. This represents a novel mechanism by which immune cells can signal to the placental unit, potentially facilitating responses to maternal inflammation and infection, and thereby preventing harm to the fetus.

Indexed as

Cell LineCytokinesExosomesFemaleHumansInflammationMacrophagesMaternal-Fetal RelationsPlacentaPregnancyTrophoblastsCytokinescytokinesendocytosisexosomesextracellular vesiclesimmunologymacrophagemicrovesiclesplacentapregnancyreproductivetrophoblast

Identifiers

PMID26602702
PMCPMC4738478
OpenAlexW2181193598

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.