Single-cell sequencing shows cellular heterogeneity of cutaneous lesions in lupus erythematosus.
Meiling ZhengZhi HuXiaole MeiLianlian OuyangYang SongWenhui ZhouYi KongRuifang WuShijia RaoHai LongWei ShiHui JingShuang LuHaijing WuSujie JiaQianjin LuMing ZhaoPublished in: Nature communications (2022)
Discoid lupus erythematosus (DLE) and systemic lupus erythematosus (SLE) are both types of lupus, yet the characteristics, and differences between them are not fully understood. Here we show single-cell RNA sequencing data of cutaneous lesions from DLE and SLE patients and skin tissues from healthy controls (HCs). We find significantly higher proportions of T cells, B cells and NK cells in DLE than in SLE. Expanded CCL20 + keratinocyte, CXCL1 + fibroblast, ISG hi CD4/CD8 T cell, ISG hi plasma cell, pDC, and NK subclusters are identified in DLE and SLE compared to HC. In addition, we observe higher cell communication scores between cell types such as fibroblasts and macrophage/dendritic cells in cutaneous lesions of DLE and SLE compared to HC. In summary, we clarify the heterogeneous characteristics in cutaneous lesions between DLE and SLE, and discover some specific cell subtypes and ligand-receptor pairs that indicate possible therapeutic targets of lupus erythematosus.
Keyphrases
- systemic lupus erythematosus
- single cell
- disease activity
- rna seq
- high throughput
- dendritic cells
- rheumatoid arthritis
- end stage renal disease
- cell therapy
- immune response
- chronic kidney disease
- stem cells
- newly diagnosed
- ejection fraction
- machine learning
- peritoneal dialysis
- artificial intelligence
- regulatory t cells
- liver fibrosis
- patient reported outcomes
- electronic health record
- big data
- deep learning