Evidence map›Paper›PMID 27389696›Full record

ArticlePloS one2016

PSG9 Stimulates Increase in FoxP3+ Regulatory T-Cells through the TGF-β1 Pathway.

Karlie Jones, Angela Ballesteros, Margaret Mentink-Kane, James Warren, Shemona Rattila, Harry Malech, Elizabeth Kang, Gabriela Dveksler

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  7. International journal of molecular sciences · 2025
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  17. Hijacking Sexual Immuno-Privilege in GBM-An Immuno-Evasion Strategy.International journal of molecular sciences · 2021
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Karlie JonesNational Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, United States of America.
Angela BallesterosNational Institute on Deafness and other Communication Disorders, NIH, Bethesda, Maryland, United States of America.
Margaret Mentink-KaneDepartment of Pathology, USUHS, Bethesda, Maryland, 20814, United States of America.
James WarrenDepartment of Pathology, USUHS, Bethesda, Maryland, 20814, United States of America.
Shemona RattilaDepartment of Pathology, USUHS, Bethesda, Maryland, 20814, United States of America.
Harry MalechNational Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, United States of America.
Elizabeth KangNational Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, United States of America.
Gabriela DvekslerDepartment of Pathology, USUHS, Bethesda, Maryland, 20814, United States of America.
Uniformed Services University of the Health Sciences · USNational Institute of Allergy and Infectious Diseases · USNational Institute on Deafness and Other Communication Disorders · US

Funding

Development and conduct of allogeneic stem cell transplant and autologous stem cell gene therapy for inherited immune deficienciesZIAAI000989 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KANG, ELIZABETH · 2009 to 2025
$12.4M
Gene Therapy Basic Research to Treat Inherited Primary Immune DeficienciesZIAAI000644 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MALECH, HARRY L · 2009 to 2025
$12.1M
Basic Research on Hematopoietic Human Stem CellsZIAAI000988 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MALECH, HARRY L · 2009 to 2019
$6.5M
6 · The paper itself

Abstract

The pregnancy-specific glycoproteins (PSGs) are a family of proteins secreted by the syncytiotrophoblast of the placenta and are the most abundant trophoblastic proteins in maternal blood during the third trimester. The human PSG family consists of 10 protein-coding genes, some of which have a possible role in maintaining maternal immune tolerance to the fetus. PSG9 was reported as a potential predictive biomarker of pre-eclampsia, a serious complication of pregnancy that has been related to immunological dysfunction at the fetal-maternal interface. Therefore, we hypothesized that PSG9 may have an immunoregulatory role during pregnancy. We found that PSG9 binds to LAP and activates the latent form of TGF-β1. In addition, PSG9 induces the secretion of TGF-β1 from macrophages but not from CD4+ T-cells. TGF-β1 is required for the ex vivo differentiation of regulatory T-cells and, consistent with the ability of PSG9 to activate this cytokine, we observed that PSG9 induces the differentiation of FoxP3+ regulatory T-cells from naïve murine and human T-cells. Cytokines that are associated with inflammatory responses were also reduced in the supernatants of T-cells treated with PSG9, suggesting that PSG9, through its activation of TGFβ-1, could be a potent inducer of immune tolerance.

Indexed as

AnimalsCell DifferentiationChemokinesFemaleForkhead Transcription FactorsHumansImmune SystemInflammationKineticsMiceMice, Inbred C57BLMice, TransgenicPregnancyPregnancy-Specific beta 1-GlycoproteinsSurface Plasmon ResonanceT-Lymphocytes, RegulatoryChemokinesForkhead Transcription FactorsFOXP3 protein, humanPregnancy-Specific beta 1-GlycoproteinsTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID27389696
PMCPMC4936685
OpenAlexW2466760217

What OpenQuestion holds

Textmetadata
LicenceCC0
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.