Evidence map›Paper›PMID 40722994›Full record

ReviewAntioxidants (Basel, Switzerland)2025

Iron-Immune Crosstalk at the Maternal-Fetal Interface: Emerging Mechanisms in the Pathogenesis of Preeclampsia.

Jieyan Zhong, Ruhe Jiang, Nan Liu, Qingqing Cai, Qi Cao, Yan Du, Hongbo Zhao

Abstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 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

7 authors.

Jieyan ZhongObstetrics & Gynecology Hospital of Fudan University, Shanghai 200433, China.
Ruhe JiangObstetrics & Gynecology Hospital of Fudan University, Shanghai 200433, China.
Nan LiuObstetrics & Gynecology Hospital of Fudan University, Shanghai 200433, China.
Qingqing CaiObstetrics & Gynecology Hospital of Fudan University, Shanghai 200433, China.
Qi CaoObstetrics & Gynecology Hospital of Fudan University, Shanghai 200433, China.
Yan DuObstetrics & Gynecology Hospital of Fudan University, Shanghai 200433, China.ORCID 0000-0001-5413-7836
Hongbo ZhaoObstetrics & Gynecology Hospital of Fudan University, Shanghai 200433, China.

Funding

This work was supported by the National Key R & D Program of China (No. 2023YFC2705801) and the Natural Science Foundation of China (No. 82371687 and 81971394 ) No. 2023YFC2705801 No. 82371687 and 81971394
6 · The paper itself

Abstract

Preeclampsia (PE) is a pregnancy-specific hypertensive disorder characterized by systemic inflammation, endothelial dysfunction, and placental insufficiency. While inadequate trophoblast invasion and impaired spiral artery remodeling have long been recognized as central to its pathogenesis, emerging evidence underscores the critical roles of dysregulated iron metabolism and its crosstalk with immune responses, particularly macrophage-mediated inflammation, in driving PE development. This review systematically explores the dynamic changes in iron metabolism during pregnancy, including increased maternal iron demand, placental iron transport mechanisms, and the molecular regulation of placental iron homeostasis. We further explore the contribution of ferroptosis, an iron-dependent form of regulated cell death driven by lipid peroxidation, to trophoblast dysfunction and pregnancy-related diseases, including PE. Macrophages, pivotal immune regulators at the maternal-fetal interface, exhibit distinct polarization states that shape tissue remodeling and immune tolerance. We outline their origin, distribution, and polarization in pregnancy, and emphasize their aberrant phenotype and function in PE. The bidirectional crosstalk between iron and macrophages is also dissected: iron shapes macrophage polarization and function, while macrophages reciprocally modulate iron homeostasis. Notably, excessive reactive oxygen species (ROS) and pro-inflammatory cytokines secreted by M1-polarized macrophages may exacerbate trophoblast ferroptosis, amplifying placental injury. Within the context of PE, we delineate how iron overload and macrophage dysfunction synergize to potentiate placental inflammation and oxidative stress. Key iron-responsive immune pathways, such as the HO-1/hepcidin axis and IL-6/TNF-α signaling, are discussed in relation to disease severity. Finally, we highlight promising therapeutic strategies targeting the iron-immune axis, encompassing three key modalities-iron chelation therapy, precision immunomodulation, and metabolic reprogramming interventions-which may offer novel avenues for PE prevention and treatment.

Indexed as

ferroptosisiron–immune axisiron metabolismmacrophagematernal–fetal interfacepreeclampsia

Identifiers

PMID40722994
PMCPMC12292184

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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.