Evidence map›Paper›PMID 40038160›Full record

ReviewInflammation research : official journal of the European Histamine Research Society ... [et al.]2025

The landscape of decidual immune cells at the maternal-fetal interface in parturition and preterm birth.

Mu Lv, Yuanhui Jia, Jiaqi Dong, Shengyu Wu, Hao Ying

Abstract readReview
In one paragraph

Review in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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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

5 authors.

Mu Lv *Department of Obstetrics, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University; Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai, 200092, China.
Yuanhui Jia *Department of Obstetrics, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University; Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai, 200092, China.
Jiaqi DongDepartment of Obstetrics, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University; Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai, 200092, China.
Shengyu WuDepartment of Obstetrics, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University; Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai, 200092, China.
Hao YingDepartment of Obstetrics, Shanghai First Maternity and Infant Hospital, School of Medicine, Tongji University; Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Shanghai, 200092, China. stephenying_2011@163.com.

Funding

Key Research Project of Pudong New Area Population and Family Planning Commission PW2020E-1National Key Research and Development Program 2022YFC2704602National Natural Science Foundation of China 82271719Program of Shanghai Academic/Technology Research Leader 23XD1402700Shanghai Municipal Science and Technology Commission Research Fund 21140903800
6 · The paper itself

Abstract

backgroundParturition is similar to an inflammatory response in which resident and infiltrating immune cells release cytokines and chemokines into the maternal-fetal interface, promoting expulsion of the fetus from the mother. The untimely activation of these inflammatory pathways can result in preterm labor. The maternal-fetal interface is composed mainly of decidual tissue and placental villous space.

objectiveThe objective of this review is to examine the role and mechanisms of decidual immune cells during parturition and preterm birth. A deeper understanding of decidual immune cells at the maternal-fetal interface could provide significant insight into parturition and preterm birth pathogenesis.

methodsWe searched major databases (including PubMed, Web of Science, and Google Scholar etc.) for literature encompassing decidual immune cells, parturition and preterm birth up to July 2024 and combined with studies found in the reference lists of the included studies.

resultsDecidual neutrophils release inflammatory mediators that facilitate parturition. The M1/M2 ratio of decidual macrophages increases among preterm birth population. Mast cells may cause uterine contractions. In parturition and preterm birth, there is an increase in CD56

conclusionThe dynamic balance of the maternal-fetal immune microenvironment plays a crucial role in maintaining human pregnancy and in the initiation of delivery. A deep understanding of the mechanism of decidual immune dysfunction is crucial for understanding the pathogenesis of preterm birth.

Indexed as

DeciduaMaternal-Fetal ExchangeParturitionPremature BirthAnimalsFemaleHumansPregnancyDecidual immune cellsMaternal–fetal interfaceParturitionPreterm birth

Identifiers

PMID40038160
PMCPMC11880140

What OpenQuestion holds

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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.