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Three‑dimensional immune cartography uncovers subclinical remodeling in psoriasis
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  • Open access
  • Published: 23 February 2026

Three‑dimensional immune cartography uncovers subclinical remodeling in psoriasis

  • Longjie Li1,2 na1,
  • Lily Vu3,4 na1,
  • Paul Drury5 na1,
  • Kok Haur Ong1,2,
  • Weimiao Yu1,2 &
  • …
  • Philip L. Tong6,7 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomarkers
  • Computational biology and bioinformatics
  • Diseases
  • Immunology
  • Medical research

Abstract

Psoriasis has a complex immune microenvironment yet most spatial analyses remain two dimensional with routine histopathology. We examined whether immunohistochemistry (IHC) combined with three-dimensional (3D) digital reconstruction can quantify the immune-epithelial architecture across the psoriatic spectrum. Serial sections from 15 psoriasis patients (with lesional and peri-lesional skin 1 cm away from the psoriatic plaque) and 52 healthy donors were reconstructed into 174 tissue stacks (10,700 whole-slide images). CD3+ T cells, CD68+ myeloid cells and mast cells were mapped in 3D including their Euclidean distance to dermal–epidermal junction (DEJ). Compared with healthy controls, CD3+ clusters were redistributed towards the superficial dermis, with reduced distance to the DEJ in peri-lesional and lesional skin in psoriatic patients; CD68+ clusters showed a similar superficial shift in established plaques. In contrast, mast cell density and DEJ proximity did not differ between groups. Averaging multiple 2D sections obscured these distributional features, underscoring the value of volumetric analysis in spatial studies. Therefore, high-resolution 3D reconstruction reliably maps the spatial dynamics of T cells, macrophages and mast cells across the psoriatic spectrum. This accessible pipeline extends routine histopathology by providing quantitative 3D spatial metrics that complement routine conventional histology and may inform integration with higher-plex spatial platforms.

Data availability

The data and code of this work will be available upon reasonable request.

Abbreviations

DP:

Digital pathology

DEJ:

Dermal-epidermal junction

MC:

Mast cell

MCT:

Mast cell tryptase

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Funding

This work was supported by the LEO Foundation Grant and the Australasian College of Dermatologist’s Scientific Research Fund. This work is also jointly supported by research funding from BII and IMCB under BMRC, A*STAR. Additionally, it is supported by the Industrial Alignment Funding - Pre-Positioning Programme – (IAF-PP Grant ID: H24J4a0044) awarded to Prof. Weimiao Yu and his iDMP lab.

Author information

Author notes
  1. Longjie Li, Lily Vu and Paul Drury contributed equally to this work.

Authors and Affiliations

  1. Intelligent Digital and Molecular Pathology (iDMP) Lab, Bioinformatics Institute (BII), Agency for Science, Technology and Research (A*STAR), 30 Biopolis Street, Singapore, Singapore

    Longjie Li, Kok Haur Ong & Weimiao Yu

  2. Institute of Molecule and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore

    Longjie Li, Kok Haur Ong & Weimiao Yu

  3. Department of Anatomical Pathology, Westmead Hospital, NSW Health, Sydney, NSW, Australia

    Lily Vu

  4. Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia

    Lily Vu

  5. Western Diagnostics Laboratory, Perth, WA, Australia

    Paul Drury

  6. Department of Dermatology, St Vincent’s Hospital, Darlinghurst, NSW, Australia

    Philip L. Tong

  7. DermScreen, Bondi Junction, Ground Floor, 35 Spring Street, Sydney, NSW, 2022, Australia

    Philip L. Tong

Authors
  1. Longjie Li
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  2. Lily Vu
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Contributions

P. T. and W. Y. conceived the project and designed the experiments; P. D. contributed to sample preparation; L. L. performed model development and validation, and data analysis; L. L. designed and prepared the figures with the assistance of K. H. O.; L. L., L. V., and P. T. wrote the manuscript with the assistance and feedback of all the other co-authors.

Corresponding authors

Correspondence to Weimiao Yu or Philip L. Tong.

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All authors of this work agreed to publish with Scientific Reports once accepted.

Competing interests

The authors declare no competing interests.

Ethical approval and consent of Participate

This study was approved by the Human Research Ethics Committee (HREC) of the Royal Prince Alfred Hospital (RPAH) Zone. Informed consent was obtained from all participants, with adherence to the National Statement on Ethical Conduct in Human Research (2007). All procedures complied with the ethical standards of the institutional and national research committees.

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Cite this article

Li, L., Vu, L., Drury, P. et al. Three‑dimensional immune cartography uncovers subclinical remodeling in psoriasis. Sci Rep (2026). https://doi.org/10.1038/s41598-026-39838-0

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  • Received: 10 September 2025

  • Accepted: 09 February 2026

  • Published: 23 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-39838-0

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Keywords

  • Digital pathology
  • Psoriasis
  • Serial sectioning
  • Tissue 3D reconstruction
  • Immune cell 3D distribution
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