bioRxivSystems BiologyPreprint
Single-cell Landscape of Immune Cells in Blood and Skin in Psoriasis
Jingwen DengiD, Michel A.M. Olde NordkampiD, Shuyan Ye, Jing‐Jie Ye, Deepak BalakiD, Wanlin Yu, Timothy R. D. J. RadstakeiD, José A. M. BorghansiD, Chuanjian LuiD, Aridaman PanditiD, Bram GerritseniD
Abstract
BackgroundPsoriasis is a systemic inflammatory disease for which there is currently no cure, in part due to an incomplete understanding of its pathophysiology. MethodsTo better understand the immune response in psoriasis, we performed single-cell RNA sequencing (scRNA-seq) on peripheral blood mononuclear cells (PBMCs) and on lesional and non-lesional skin samples from a cohort of 11 psoriasis patients and 8 healthy controls. Additionally, we conducted flow cytometry on PBMCs from a separate cohort of 13 psoriasis patients and 11 ankylosing spondylitis. FindingsOur study revealed altered immune signatures of specific myeloid and lymphocyte subsets in blood and skin, both in terms of cell numbers and gene expression. Specifically, we discovered elevated proportions of circulating CD14++ monocytes, increased expression of major histocompatibility complex (MHC) class II molecule by circulating CD16+ monocytes, as well as increased expression of genes related to skin homing and to pro-inflammatory responses in psoriasis by circulating plasmacytoid dendritic cells (pDCs). Circulating CD8+ T effector memory cells in psoriasis patients exhibited reduced abundance but increased skin-homing potential. In psoriatic lesions, we observed a hyperinflammatory myeloid-cell state and enrichment of IL17-producing cells with a tissue-resident memory T-cell signature. InterpretationThe changes in immune cell numbers and gene expression indicate a significant alteration in the immune landscape of psoriasis patients. This suggests that the immune system in psoriasis is reprogrammed, affecting both innate and adaptive branches. These findings provide new insights into the aberrant immune-cell signatures in the circulation and skin lesions in psoriasis, and thereby help to understand its pathophysiology. FundingThis study was financially supported by the National Natural Science Foundation of China (U23A6012), Science and Technology Planning Project of Guangzhou (2024A03J0055, 202206080005), Innovation Team and Talents Cultivation Program of National Administration of Traditional Chinese Medicine (ZYYCXTD-C-202204).
- organism: human
- assay: scRNA-seq
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: clustering
- approach: statistical model
- approach: experimental assay
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Single Cell Analysis of pBMCs of Psoriasis patients reveals distinct CD4+ T cell phenotypes associated with response to IL-23 blockade.
Kathryne E. Marks, Anina Sun, … Brittany Weber·bioRxiv·Nov 4, 2025
- High-resolution analysis of T cell subsets, clonality, and trajectories in psoriasis
Xin Luo, Jared H. Liu, … Wilson J. Liao·bioRxiv·Oct 28, 2026
- Transcriptomic profiling of plaque psoriasis and cutaneous T cell subsets during treatment with secukinumab
Jared Liu, Hsin-Wen Chang, … Wilson J. Liao·JID InnovationsPeer-reviewed·Dec 30, 2021
- Skin inflammation driven by differentiation of quiescent tissue-resident ILCs into a spectrum of pathogenic effectors
P. Bielecki, S. J. Riesenfeld, … R. A. Flavell·bioRxiv·Nov 12, 2018
- Interleukin-36 promotes systemic Type-I IFN responses in severe psoriasis.
M. Catapano, M. Vergnano, … F. Capon·bioRxiv·Dec 14, 2018
- A transcriptional continuum from clinically normal to lesional skin: Single-cell trajectory analysis of psoriasis
Gulnur Uzun, Deniz Konak, … Pınar Pir·bioRxiv·Sep 21, 2026