Evidence map›Paper›PMID 41789068›Full record

ArticleFrontiers in immunology2026

Dysfunctional decidual CD2

Mingke Qiu, Junyi Zhang, Yujie Luo, Xinhang Meng, Songcun Wang, Liyuan Cui

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

Mingke Qiu *Department of Interventional Vascular Surgery, Xinhua Hospital, Shanghai JiaoTong University, School of Medicine, Shanghai, China.
Junyi Zhang *Department of Interventional Vascular Surgery, Xinhua Hospital, Shanghai JiaoTong University, School of Medicine, Shanghai, China.
Yujie LuoLaboratory for Reproductive Immunology, Obstetrics & Gynecology Hospital of Fudan University, Shanghai, China.
Xinhang MengLaboratory for Reproductive Immunology, Obstetrics & Gynecology Hospital of Fudan University, Shanghai, China.
Songcun WangLaboratory for Reproductive Immunology, Obstetrics & Gynecology Hospital of Fudan University, Shanghai, China.
Liyuan CuiLaboratory for Reproductive Immunology, Obstetrics & Gynecology Hospital of Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The multifactorial nature of recurrent pregnancy loss (RPL) requires a comprehensive understanding of its diverse risk factors, including sleep disturbance. Previously, we reported decreased Rev-erbα expression in decidual stromal cells from pregnant mice with sleep disturbance (SD) and patients of RPL with sleep disturbance (RS). Methods: Omics analyses were used to predict the interaction between Rev-erbα and glutamine-fructose-6-phosphate amidotransferase 1 (GFPT1). Tunicamycin and peptide-N-glycosidase F and phosphatidylinositol-specific phospholipase C treatment were conducted to analyze the glycosylation modification type of CD58. The coculture between decidual immune cells and decidual stroma cells (DSCs) in which Rev-erbα, GFPT1, or CD58 was either knockdown or overexpressed was performed to evaluate the crosstalk of CD58 Results: We found that glycometabolism related GFPT1, which regulated by Rev-erbα, increased CD58 expression via glycosylphosphatidylinositol modification not classical N- or O-linked glycosylation modification, leading to the disorder of decidual CD2 Conclusions: Rev-erbα - GFPT1 - CD58 - CD2 axis played important role in pregnancy maintenance by regulating the crosstalk between DSCs and decidual CD4

Indexed as

Abortion, HabitualCD4-Positive T-LymphocytesDeciduaNuclear Receptor Subfamily 1, Group D, Member 1Stromal CellsAnimalsCD2 AntigensDisease Models, AnimalFemaleHumansMicePregnancyCD2 AntigensNuclear Receptor Subfamily 1, Group D, Member 1CD2GFPT1glycosylphosphatidylinositolrecurrent pregnancy losssleep disturbance

Identifiers

PMID41789068
PMCPMC12956714

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.