» Articles » PMID: 38894741

Unveiling Immune Tolerance Pathways in Preeclampsia Placenta: Implications for Molecular Targets and Discovery of Potential Biomarkers

Overview
Specialty Endocrinology
Date 2024 Jun 19
PMID 38894741
Authors
Affiliations
Soon will be listed here.
Abstract

During pregnancy, there is a link between disruption of maternal immune tolerance and preeclampsia, but the molecular mechanisms that regulate maternal and fetal immune tolerance remain unclear. This study employs bioinformatics to identify new markers related to placental immune tolerance and explore their potential role in predicting preeclampsia. Analyzing preeclampsia-related gene expression profiles in the Gene Expression Omnibus (GEO) dataset reveals 211 differentially expressed genes (DEGs) in the placenta, mainly influencing immune cell differentiation and response pathways. Employing weighted gene co-expression network analysis (WGCNA) and lasso regression, four potential target genes (ANKRD37, CRH, LEP, SIGLEC6) are identified for potential prediction of preeclampsia. Validation using the GSE4707 dataset confirmed the diagnostic and predictive potential of these candidate genes. RT-qPCR verified up-regulation in the placenta, while ELISA showed their correlation with immune tolerance factors associated with placental immune tolerance. As a result of this study, identifies potential biomarkers associated with placental immunity and contributes to understanding the molecular mechanism of preeclampsia.

Citing Articles

Evaluation of placental growth factor, Vitamin D, and systemic inflammatory index as predictive biomarkers for preeclampsia severity: a retrospective cohort study.

Han X, Yang H BMC Pregnancy Childbirth. 2025; 25(1):75.

PMID: 39871211 PMC: 11771059. DOI: 10.1186/s12884-025-07187-x.

References
1.
Chang G, Yang X, Liu W, Lin S, Yang S, Zhao M . FABP4 facilitates inflammasome activation to induce the Treg/Th17 imbalance in preeclampsia via forming a positive feedback with IL-17A. Mol Ther Nucleic Acids. 2021; 24:743-754. PMC: 8094592. DOI: 10.1016/j.omtn.2021.03.020. View

2.
Pankiewicz K, Fijalkowska A, Issat T, Maciejewski T . Insight into the Key Points of Preeclampsia Pathophysiology: Uterine Artery Remodeling and the Role of MicroRNAs. Int J Mol Sci. 2021; 22(6). PMC: 8003365. DOI: 10.3390/ijms22063132. View

3.
Puangpetch A, Unaharassamee W, Jiratjintana N, Koomdee N, Sukasem C . Genetic polymorphisms of HTR2C, LEP and LEPR on metabolic syndromes in patients treated with atypical antipsychotic drugs. J Pharm Pharmacol. 2018; 70(4):536-542. DOI: 10.1111/jphp.12892. View

4.
Stenzel-Poore M, Duncan J, RITTENBERG M, Bakke A, Heinrichs S . CRH overproduction in transgenic mice: behavioral and immune system modulation. Ann N Y Acad Sci. 1996; 780:36-48. DOI: 10.1111/j.1749-6632.1996.tb15110.x. View

5.
Lindberger E, Ahlsson F, Junus K, Kallak T, Lager S, Callbo P . Early Mid-pregnancy Blood-Based Proteins as Possible Biomarkers of Increased Infant Birth Size in Sex-Stratified Analyses. Reprod Sci. 2022; 30(4):1165-1175. PMC: 9524307. DOI: 10.1007/s43032-022-01093-9. View