Evidence map›Paper›PMID 24793405›Full record

ArticleCellular & molecular immunology2015

CD56(bright)CD25+ NK cells are preferentially recruited to the maternal/fetal interface in early human pregnancy.

Yu Tao, Yan-Hong Li, Hai-Lan Piao, Wen-Jie Zhou, Di Zhang, Qiang Fu, Song-Cun Wang, Da-Jin Li, Mei-Rong Du

Open access · bronzeAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

31 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. CD25Oncoimmunology · 2023
    Article
  8. Article
  9. Human Chorionic Villous Differentiation and Placental Development.International journal of molecular sciences · 2022
    Review
  10. Dysfunction of CCR1Frontiers in immunology · 2022
    Article
  11. Review
  12. Regulation and Function of Chemokines at the Maternal-Fetal Interface.Frontiers in cell and developmental biology · 2022
    Review
  13. Decidual CXCR4Clinical and translational medicine · 2021
    Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. PlGF Immunological Impact during Pregnancy.International journal of molecular sciences · 2020
    Review
  19. Article
  20. Review
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

9 authors at 1 institution in 1 country.

Yu Tao
Yan-Hong Li
Hai-Lan Piao
Wen-Jie Zhou
Di Zhang
Qiang Fu
Song-Cun Wang
Da-Jin Li
Mei-Rong Du
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decidual natural killer (dNK) cells are believed to be critical for maintaining maternal/fetal tolerance and regulating placental vascular remodeling based upon their abundance and unique phenotype during early pregnancy. However, the mechanism for how the dNK cells play such important roles in successful pregnancy remains undefined. Here, we identified a subtype of dNK cells characterized as having a CD3(-)CD56(bright)CD25(+) phenotype. We found that CD56(bright)CD25(+) NK cells preferentially localize to the maternal/fetal interface during early human pregnancy. CD25(+) dNK cells account for approximately 75% of CD25-expressing decidual immune cells (DICs). However, less than 5% of CD25-positive peripheral blood mononuclear cells are CD25(+) NK cells. Furthermore, CD25(+) and CD25(-) dNK cells exhibit distinct phenotypes: CD25(+) dNK cells display a more activated phenotype and greater cytokine-secreting capacity. Interestingly, coculture of peripheral NK (pNK) cells with primary trophoblasts upregulates the percentage of CD25-expressing pNK cells, resulting in increased expression of activation markers and cytokine production by pNK cells. In addition, we demonstrated that the CXCL12/CXCR4 axis is crucial for the recruitment of CD25(+) dNK cells and contributes to the accumulation of CD3(-)CD56(bright)CD25(+) dNK cells at the maternal/fetal interface. Thus, our data reveal that the crosstalk between trophoblasts and pNK cells leads to the accumulation of CD3(-)CD56(bright)CD25(+) dNK cells, which exert a regulating effect at the maternal/fetal interface.

Indexed as

CD56 AntigenCell CommunicationCell MovementCells, CulturedChemokine CXCL12Coculture TechniquesCytokinesFemaleHumansImmunophenotypingInterleukin-2 Receptor alpha SubunitKiller Cells, NaturalLymphocyte ActivationLymphocyte SubsetsMaternal-Fetal ExchangePregnancyCD56 AntigenChemokine CXCL12CXCR4 protein, humanCytokinesInterleukin-2 Receptor alpha SubunitReceptors, CXCR4

Identifiers

PMID24793405
PMCPMC4654367
OpenAlexW1990877151

What OpenQuestion holds

Textmetadata
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.