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Table · dataset · 2026

Immune cell enrichment characteristics and related key genes in intrauterine adhesion: insights from RNA-sequencing analysis

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<p>Intrauterine adhesion (IUA) represents a prevalent cause of persistent infertility and continues to be a significant unresolved challenge in reproductive medicine.

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However, its full pathogenic mechanisms remain incompletely elucidated. We retrieved endometrial RNA-sequencing data from IUA patients and normal controls in the Gene Expression Omnibus (GEO) database, and screened 586 differentially expressed genes (DEGs) in the endometrium of IUA patients using the R package limma.

Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and gene set enrichment analysis (GSEA) revealed activation of immune-related pathways, including chronic inflammatory response, complement activation, and complement and coagulation cascades in IUA. Further single-sample gene set enrichment analysis (ssGSEA)-based relative immune cell enrichment analysis revealed decreased enrichment scores of activated CD4 T cells and type 2 T helper cells, alongside increased enrichment scores of effector memory CD8 T cells, macrophages, mast cells, natural killer cells, and T follicular helper cells in IUA patients, indicating their potential involvement in IUA pathogenesis.

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A protein–protein interaction (PPI) network was constructed, identifying 10 hub genes associated with IUA: <i>CDK1</i>, <i>CCNB1</i>, <i>CCNA2</i>, <i>CENPA</i>, <i>BUB1</i>, <i>AURKB</i>, <i>KIF11</i>, <i>BUB1B</i>, <i>CDC20</i>, and <i>TOP2A</i>. The expression patterns of these genes were further validated in two independent external IUA cohorts, supporting a potential correlative link between these genes and IUA pathogenesis.

Our findings provide exploratory insights and potential candidate molecules for subsequent mechanistic studies of IUA onset and progression.</p>

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concepts[field].anzsrc:group:3204mapping · figshare comvocabulary-mapper@1.0.0keywords['Immunology']
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