Evidence map›Paper›PMID 33193353›Full record

ArticleFrontiers in immunology2020

Visualizing Dynamic Changes at the Maternal-Fetal Interface Throughout Human Pregnancy by Mass Cytometry.

Anita van der Zwan, Vincent van Unen, Guillaume Beyrend, Sandra Laban, Carin van der Keur, Hanneke J M Kapsenberg, Thomas Höllt, Susana M Chuva de Sousa Lopes, Marie-Louise P van der Hoorn, Frits Koning and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 49 citations in OpenAlex.

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  10. CD4Frontiers in immunology · 2024
    Article
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  15. Article
  16. The role of neutrophils in chorioamnionitis.Frontiers in immunology · 2023
    Review
  17. Article
  18. Article
  19. Single-Cell Immunobiology of the Maternal-Fetal Interface.Journal of immunology (Baltimore, Md. : 1950) · 2022
    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

13 authors at 1 institution in 2 countries.

Anita van der ZwanDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Vincent van UnenDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Guillaume BeyrendDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Sandra LabanDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Carin van der KeurDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Hanneke J M KapsenbergDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Thomas HölltLeiden Computational Biology Center, Leiden University Medical Center, Leiden, Netherlands.
Susana M Chuva de Sousa LopesDepartment of Anatomy and Embryology, Leiden University Medical Center, Leiden, Netherlands.
Marie-Louise P van der HoornDepartment of Obstetrics and Gynaecology, Leiden University Medical Center, Leiden, Netherlands.
Frits KoningDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Frans H J ClaasDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Michael EikmansDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Sebastiaan HeidtDepartment of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During healthy pregnancy, a balanced microenvironment at the maternal-fetal interface with coordinated interaction between various immune cells is necessary to maintain immunological tolerance. While specific decidual immune cell subsets have been investigated, a system-wide unbiased approach is lacking. Here, mass cytometry was applied for data-driven, in-depth immune profiling of the total leukocyte population isolated from first, second, and third trimester decidua, as well as maternal peripheral blood at time of delivery. The maternal-fetal interface showed a unique composition of immune cells, different from peripheral blood, with significant differences between early and term pregnancy samples. Profiling revealed substantial heterogeneity in the decidual lymphoid and myeloid cell lineages that shape gestational-specific immune networks and putative differentiation trajectories over time during gestation. Uncovering the overall complexity at the maternal-fetal interface throughout pregnancy resulted in a human atlas that may serve as a foundation upon which comprehension of the immune microenvironment and alterations thereof in pregnancy complications can be built.

Indexed as

PregnancyAdultCells, CulturedCellular MicroenvironmentDeciduaFemaleFlow CytometryHumansImmune ToleranceImmunophenotypingLeukocytesLymphocytesPerinatologyPlacentaPregnancy Complicationsdeciduahuman atlasimmune profilingperipheral bloodplacentapregnancy

Identifiers

PMID33193353
PMCPMC7649376
OpenAlexW3097959134

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.