Evidence map›Paper›PMID 31244846›Full record

ArticleFrontiers in immunology2019

Recruitment of MAIT Cells to the Intervillous Space of the Placenta by Placenta-Derived Chemokines.

Martin Solders, Laia Gorchs, Eleonor Tiblad, Sebastian Gidlöf, Edwin Leeansyah, Joana Dias, Johan K Sandberg, Isabelle Magalhaes, Anna-Carin Lundell, Helen Kaipe

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

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  11. Synergistic effects of radiotherapy and targeted immunotherapy in improving tumor treatment efficacy: a review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  12. Review
  13. Single-Cell Immunobiology of the Maternal-Fetal Interface.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  14. Article
  15. Review
  16. Multiomic analysis reveals decidual-specific transcriptional programing of MAIT cells.American journal of reproductive immunology (New York, N.Y. : 1989) · 2021
    Article
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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

10 authors at 4 institutions in 2 countries.

Martin SoldersClinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.
Laia GorchsDepartment of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Eleonor TibladCenter for Fetal Medicine, Karolinska University Hospital and Department of CLINTEC, Karolinska Insitutet, Stockholm, Sweden.
Sebastian GidlöfCenter for Fetal Medicine, Karolinska University Hospital and Department of CLINTEC, Karolinska Insitutet, Stockholm, Sweden.
Edwin LeeansyahCenter for Infectious Medicine, Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.
Joana DiasCenter for Infectious Medicine, Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.
Johan K SandbergCenter for Infectious Medicine, Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.
Isabelle MagalhaesDepartment of Oncology/Pathology, Karolinska Institutet, Stockholm, Sweden.
Anna-Carin LundellDepartment of Rheumatology and Inflammation Research, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Helen KaipeClinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SENational University of Singapore · SGUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intervillous space of the placenta is a part of the fetal-maternal interface, where maternal blood enters to provide nutrients and gas exchange. Little is known about the maternal immune cells at this site, which are in direct contact with fetal tissues. We have characterized the T cell composition and chemokine profile in paired intervillous and peripheral blood samples from healthy mothers giving birth following term pregnancies. Mucosal-associated invariant T (MAIT) cells and effector memory (EM) T cells were enriched in the intervillous blood compared to peripheral blood, suggesting that MAIT cells and other EM T cells home to the placenta during pregnancy. Furthermore, pregnant women had lower proportions of peripheral blood MAIT cells compared to non-pregnant women. The levels of several chemokines were significantly higher in intervillous compared to peripheral blood, including macrophage migration inhibitory factor (MIF), CXCL10, and CCL25, whereas CCL21, CCL27 and CXCL12 were lower. Migration assays showed that MAIT cells and EM T cells migrated toward conditioned medium from placental explants. A multivariate factor analysis indicated that high levels of MIF and CCL25 were associated with high proportions of MAIT cells in intervillous blood. Blocking of MIF or a combination of MIF, CCL25, and CCL20 in migration assays inhibited MAIT cell migration toward placenta conditioned medium. Finally, MAIT cells showed migratory capacities toward recombinant MIF. Together, these findings indicate that term placental tissues attract MAIT cells, and that this effect is at least partly mediated by MIF.

Indexed as

AdultCell MovementChemokines, CXCFemaleFetusHumansMacrophage Migration-Inhibitory FactorsMucosal-Associated Invariant T CellsPlacentaPregnancyYoung AdultChemokines, CXCMacrophage Migration-Inhibitory Factorschemokinesintervillous spaceMAIT cellsMIFplacentareproductive immunologyT cells

Identifiers

PMID31244846
PMCPMC6563723
OpenAlexW2949004468

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.