Evidence map›Paper›PMID 26987775›Full record

ArticleScientific reports2016

Human Umbilical Vein Endothelial Cells foster conversion of CD4+CD25-Foxp3- T cells into CD4+Foxp3+ Regulatory T Cells via Transforming Growth Factor-β.

Anika Oettel, Mario Lorenz, Verena Stangl, Serban-Dan Costa, Ana Claudia Zenclussen, Anne Schumacher

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. 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

6 authors at 2 institutions in 1 country.

Anika OettelExperimental Obstetrics and Gynecology, Medical Faculty, Otto-von-Guericke University, Gerhart-Hauptmann-Straße 35, 39108 Magdeburg, Germany.
Mario LorenzMedical Clinic for Cardiology and Angiology, Campus Mitte, Charite - Universitätsmedizin Berlin, Germany, Charitéplatz 1, 10117 Berlin, Germany.
Verena StanglMedical Clinic for Cardiology and Angiology, Campus Mitte, Charite - Universitätsmedizin Berlin, Germany, Charitéplatz 1, 10117 Berlin, Germany.
Serban-Dan CostaUniversity Women's Clinic, Otto-von-Guericke University, Gerhart-Hauptmann-Straße 35, 39108 Magdeburg, Germany.
Ana Claudia ZenclussenExperimental Obstetrics and Gynecology, Medical Faculty, Otto-von-Guericke University, Gerhart-Hauptmann-Straße 35, 39108 Magdeburg, Germany.
Anne SchumacherExperimental Obstetrics and Gynecology, Medical Faculty, Otto-von-Guericke University, Gerhart-Hauptmann-Straße 35, 39108 Magdeburg, Germany.
Otto-von-Guericke University Magdeburg · DECharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trans-placental cell trafficking is a naturally occurring process during pregnancy that results in the direct recognition of foreign maternal antigens by fetal tissue and vice versa. Immigration of potentially harmful allo-reactive maternal T cells into fetal circulation may provoke anti-fetal immune responses. However, the contact with fetal tissue may favor differentiation of maternal immune cells into cells with a regulatory phenotype. Human Umbilical Vein Endothelial Cells (HUVECs) possess immune-regulating properties and are one of the first fetal cells to get in contact with foreign maternal immune cells. Therefore, here we studied whether HUVECs induce the conversion of maternal T cells into regulatory T (Treg) cells. Moreover, we assessed whether this response is changing according to the sex of the HUVECs. Both female and male HUVECs induced the conversion of maternal T cells into Treg cells which is partially mediated via TGF-β. Female HUVECs showed a stronger capacity to induce Treg cells compared to male HUVECs. Our findings propose that HUVECs contribute to fetal-maternal tolerance by the increase of the Treg cell population. Sex-specific differences in Treg cell induction may partly account for the disparities on the incidence of infectious and autoimmune diseases between both sexes during early childhood.

Indexed as

AdultCD4-Positive T-LymphocytesCell DifferentiationCell ProliferationCells, CulturedCoculture TechniquesFemaleForkhead Transcription FactorsGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsMalePregnancyT-Lymphocytes, RegulatoryTransforming Growth Factor betaForkhead Transcription FactorsFOXP3 protein, humanTransforming Growth Factor beta

Identifiers

PMID26987775
PMCPMC4796866
OpenAlexW2297551155

What Socratic 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 Socratic graph.