0964: A Single-cell Atlas Reveals Dermal Endothelial Heterogeneity and Disease-specific Pathways in Autoimmune Disorders

Background/Purpose: Autoimmune conditions with skin involvement, including scleroderma (SSc), antiphospholipid syndrome (APS), systemic lupus erythematosus (SLE) and psoriasis (PSO), involve intricate interactions between immune cells and the vasculature, with endothelial cells (ECs) playing a critical role in disease pathogenesis. To elucidate the diverse functional roles of ECs in these conditions, we constructed a comprehensive single-cell atlas by integrating single-cell RNA sequencing (scRNA-seq) data from affected and healthy skin biopsies.

Methods: Skin biopsies from patients were analyzed using 10x Genomics scRNA-seq. Publicly available datasets from SSc (GSE249279), APS (GSE290946), SLE (GSE186476), PSO (GSE173706), and healthy controls (GSE249279 and GSE290946), generated using the same platform, were integrated (Figure 1A). Skin biopsies from active skin of patients were analyzed using 10x Genomics scRNA-seq. Cell identities, gene expression profiles, and pathway activities were analyzed across endothelial and stromal populations.

Results: We profiled 23,410 endothelial and stromal cells, identifying arterial, venous, capillary, and lymphatic ECs, as well as pericytes and vascular smooth muscle cells (VSMCs) from all scRNA-seq datasets. Arterial and venous ECs were significantly reduced in SSc, while VSMCs were markedly increased. APS samples showed an expansion of arterial, capillary and venous ECs, whereas SLE and PSO exhibited cellular compositions similar to healthy controls (Figure 1). Pathway enrichment analysis of EC gene expression revealed both shared and disease-specific programs (Figure 2). Across autoimmune conditions, common signatures relative to healthy controls included NF-κB signaling, leukocyte adhesion, and antigen presentation. APS-derived ECs were further enriched for antigen presentation, oxidized LDL response, leukocyte adhesion, and T cell activation pathways. SLE samples demonstrated prominent type I interferon responses, while SSc samples exhibited strong enrichment of intrinsic apoptotic pathways. No dominant pathway activation was observed in PSO.

Deeper subclustering of vascular ECs defined seven endothelial subtypes, including SENA3G+ arterial ECs, RGCC+ capillary ECs, TLL1⁺ venous ECs, hypoxia-associated ECs, EndoMT, cycling ECs, and a previously undefined subset IL6⁺ venous ECs (Figure 3). IL6⁺ and EndoMT ECs were enriched in SSc and expressed pro-inflammatory, senescence-associated, and matrix remodeling genes. SLE and PSO had elevated IL6+ EC and cycling EC populations, potentially driving immune dysregulation and vascular proliferation linked to systemic organ damage. APS was marked by abundant EndoMT+ ECs, suggesting endothelial plasticity. Senescence and EndoMT scores were highest in SSc, followed by APS and SLE, and minimal in PSO.

Conclusion: This single-cell atlas defines dermal endothelial heterogeneity across autoimmune diseases. Notably, we identified a novel IL6⁺ EC subset enriched in SSc with pro-inflammatory and senescence signatures, and revealed distinct EC programs across diseases. These findings highlight EC subtype dynamics as potential contributors to immune dysregulation and fibrotic remodeling.