Evidence map›Paper›PMID 37008954›Full record

ArticleFrontiers in endocrinology2023

The immune checkpoint molecule, VTCN1/B7-H4, guides differentiation and suppresses proinflammatory responses and MHC class I expression in an embryonic stem cell-derived model of human trophoblast.

Jie Zhou, Yuchen Tian, Ying Qu, Madyson Williams, Ye Yuan, Rowan M Karvas, Megan A Sheridan, Laura C Schulz, Toshihiko Ezashi, Michael R Roberts and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

11 authors at 4 institutions in 1 country.

Jie ZhouDepartment of Obstetrics, Gynecology, and Women's Health, University of Missouri, Columbia, MO, United States.
Yuchen TianBond Life Sciences Center, University of Missouri, Columbia, MO, United States.
Ying QuDepartment of Obstetrics, Gynecology, and Women's Health, University of Missouri, Columbia, MO, United States.
Madyson WilliamsDepartment of Obstetrics, Gynecology, and Women's Health, University of Missouri, Columbia, MO, United States.
Ye YuanResearch Department, Colorado Center for Reproductive Medicine, Lone Tree, CO, United States.
Rowan M KarvasDepartment of Developmental Biology, Washington University School of Medicine, St. Louis, MO, United States.
Megan A SheridanDepartment of Obstetrics, Gynecology, and Women's Health, University of Missouri, Columbia, MO, United States.
Laura C SchulzDepartment of Obstetrics, Gynecology, and Women's Health, University of Missouri, Columbia, MO, United States.
Toshihiko EzashiResearch Department, Colorado Center for Reproductive Medicine, Lone Tree, CO, United States.
Michael R RobertsBond Life Sciences Center, University of Missouri, Columbia, MO, United States.
Danny J SchustDepartment of Obstetrics, Gynecology, and Women's Health, University of Missouri, Columbia, MO, United States.
University of Missouri · USUniversity of Missouri Health System · USColorado Center for Reproductive Medicine · USWashington University in St. Louis · US

Funding

Modeling Normal and Abnormal TrophoblastsR01HD094937 · NICHD · UNIVERSITY OF MISSOURI-COLUMBIA · PI R. MICHAEL ROBERTS, Laura Clamon SCHULZ · 2018 to 2026
$4.5M
VTCN1 regulation of MHC in early human placental developmentR21AI145071 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI EZASHI, TOSHIHIKO, SCHUST, DANNY J · 2020 to 2021
$426k
NIAID NIH HHS R21 AI145071NICHD NIH HHS R01 HD094937
6 · The paper itself

Abstract

The placenta acts as a protective barrier to pathogens and other harmful substances present in the maternal circulation throughout pregnancy. Disruption of placental development can lead to complications of pregnancy such as preeclampsia, intrauterine growth retardation and preterm birth. In previous work, we have shown that expression of the immune checkpoint regulator, B7-H4/VTCN1, is increased upon differentiation of human embryonic stem cells (hESC) to an

Indexed as

Premature BirthTrophoblastsCell DifferentiationEmbryonic Stem CellsFemaleHistocompatibility Antigens Class IHLA AntigensHumansImmune Checkpoint ProteinsInfant, NewbornPlacentaPregnancyV-Set Domain-Containing T-Cell Activation Inhibitor 1Histocompatibility Antigens Class IHLA AntigensImmune Checkpoint ProteinsV-Set Domain-Containing T-Cell Activation Inhibitor 1VTCN1 protein, humananti-viral responsesB7-H4/VTCN1classical major histocompatibility complex class I molecules (MHC-I)embryonic stem cellsHLA-Gnatural killer cellsplacental developmentvirus

Identifiers

PMID37008954
PMCPMC10062451
OpenAlexW4327571486

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.