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LILRB4 is associated with macrophages in the OC immune microenvironment. (A) Correlation of StromalScore, ImmuneScore, and ESTIMATEScore with LILRB4 expression in TCGA-OV patients. (B) UMAP visualization of single-cell RNA-seq data from the OV_EMTAB8107 tumor dataset (left) and corresponding LILRB4 expression across different cell clusters (right). (C) Distribution of LILRB4 expression across various cell types in GEO-derived single-cell datasets, analyzed using the TISCH2 database ( http://tisch.comp-genomics.org/ ), with darker colors indicating higher expression levels. (D) Correlation between macrophage enrichment scores and LILRB4 expression in TCGA-OV samples, as determined by ssGSEA. (E) Relative mRNA expression of F4/80 in orthotopic ovarian tumor models (NC and sh-LILRB4 groups). (F) Representative IHC images showing F4/80 expression in orthotopic ovarian tumors (n = 3). Scale bar, 100 μm. (G) Representative IHC staining of CD68 and LILRB4 in corresponding regions of human OC tissues (n = 3). All panels are shown at the same magnification. Scale bar, 100 μm. Data are presented as mean ± SD. Statistical analysis was performed using unpaired two-tailed Student’s t-test. *p < 0.05, ****p < 0.0001.

Journal: Frontiers in Immunology

Article Title: Identification of LILRB4 as a regulator of M2c macrophages and a potential immunotherapeutic target in ovarian cancer

doi: 10.3389/fimmu.2026.1866073

Figure Lengend Snippet: LILRB4 is associated with macrophages in the OC immune microenvironment. (A) Correlation of StromalScore, ImmuneScore, and ESTIMATEScore with LILRB4 expression in TCGA-OV patients. (B) UMAP visualization of single-cell RNA-seq data from the OV_EMTAB8107 tumor dataset (left) and corresponding LILRB4 expression across different cell clusters (right). (C) Distribution of LILRB4 expression across various cell types in GEO-derived single-cell datasets, analyzed using the TISCH2 database ( http://tisch.comp-genomics.org/ ), with darker colors indicating higher expression levels. (D) Correlation between macrophage enrichment scores and LILRB4 expression in TCGA-OV samples, as determined by ssGSEA. (E) Relative mRNA expression of F4/80 in orthotopic ovarian tumor models (NC and sh-LILRB4 groups). (F) Representative IHC images showing F4/80 expression in orthotopic ovarian tumors (n = 3). Scale bar, 100 μm. (G) Representative IHC staining of CD68 and LILRB4 in corresponding regions of human OC tissues (n = 3). All panels are shown at the same magnification. Scale bar, 100 μm. Data are presented as mean ± SD. Statistical analysis was performed using unpaired two-tailed Student’s t-test. *p < 0.05, ****p < 0.0001.

Article Snippet: All antibodies used in this study were commercially available: LILRB4 (A7073; ABclonal, Wuhan, China; 1:2000 for WB and 1:200 for immunohistochemistry), glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (AB2100; NCM Biotech, Suzhou, China; 1:20,000), F4/80 (A27257; ABclonal, Wuhan, China; 1:200), Ki67 (A20018; ABclonal, Wuhan, China; 1:200), CD68 (A24386PM; ABclonal, Wuhan, China; 1:200), phospho-NF-κB (p-NF-κB; TP56372; Abmart, Shanghai, China; 1:1000), CD163 (A8383SP; ABclonal, Wuhan, China; 1:200), CD8 (A23081; ABclonal, Wuhan, China; 1:200), granzyme B (GZMB) (A2557; ABclonal, Wuhan, China; 1:200), and goat anti-rabbit IgG (H+L)-HRP conjugate (LF102; Epizyme Biotech, Shanghai, China; 1:3000).

Techniques: Expressing, Single Cell, RNA Sequencing, Derivative Assay, Immunohistochemistry, Two Tailed Test