Evidence map›Paper›PMID 35811852›Full record

ArticleiScience2022

Imaging mass cytometry reveals the prominent role of myeloid cells at the maternal-fetal interface.

Juliette Krop, Anita van der Zwan, Marieke E Ijsselsteijn, Hanneke Kapsenberg, Sietse J Luk, Sanne H Hendriks, Carin van der Keur, Lotte J Verleng, Antonis Somarakis, Lotte van der Meeren and 9 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 46 citations in OpenAlex.

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  5. Insights into the maternal-fetal interface from spatial multi-omics.Frontiers in cell and developmental biology · 2026
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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

19 authors at 1 institution in 1 country.

Juliette KropDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Anita van der ZwanDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Marieke E IjsselsteijnDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Hanneke KapsenbergDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Sietse J LukDepartment of Haematology, Leiden University Medical Center, Leiden, the Netherlands.
Sanne H HendriksDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Carin van der KeurDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Lotte J VerlengDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Antonis SomarakisDivision of Image Processing, Leiden University Medical Center, Leiden, the Netherlands.
Lotte van der MeerenDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Geert HaasnootDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Manon BosDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Noel F C C de MirandaDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Susana M Chuva de Sousa LopesDepartment of Anatomy and Embryology, Leiden University Medical Center, Leiden, the Netherlands.
Marie-Louise P van der HoornDepartment of Gynecology and Obstetrics, Leiden University Medical Center, Leiden, the Netherlands.
Frits KoningDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Frans H J ClaasDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Sebastiaan HeidtDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Michael EikmansDepartment of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the immunological complexity of the maternal-fetal interface is well appreciated, the actual interaction of maternal immune cells and fetal trophoblasts is insufficiently understood. To comprehend the composition and spatial orientation of maternal immune cells and fetal extravillous trophoblasts, we applied imaging mass cytometry on decidua basalis of the three trimesters of healthy pregnancy. Within all trimesters, we observed considerably higher frequencies of myeloid cells in the decidua than is seen with single-cell suspension techniques. Moreover, they were the most pronounced cell type in the microenvironment of other decidual cells. In first trimester, HLA-DR

Indexed as

Biological sciencesBiological sciences research methodologiesBiotechnologyImmunology

Identifiers

PMID35811852
PMCPMC9257341
OpenAlexW4283157058

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.