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Automated cell annotation and classification on histopathology for spatial biomarker discovery

Author

Listed:
  • Zhe Li

    (Stanford University School of Medicine)

  • Seyed Hossein Mirjahanmardi

    (Stanford University School of Medicine)

  • Rasoul Sali

    (Stanford University School of Medicine)

  • Feyisope Eweje

    (Stanford University School of Medicine)

  • Matthew Gopaulchan

    (Stanford University School of Medicine)

  • Leon Kloker

    (Institute for Computational & Mathematical Engineering)

  • Xiaoming Zhang

    (Stanford University School of Medicine)

  • Guoxin Li

    (Southern Medical University)

  • Yuming Jiang

    (Stanford University School of Medicine
    Wake Forest University School of Medicine)

  • Ruijiang Li

    (Stanford University School of Medicine
    Stanford Institute for Human-Centered Artificial Intelligence)

Abstract

Histopathology with hematoxylin and eosin (H&E) staining is routinely employed for clinical diagnoses. Single-cell analysis of histopathology provides a powerful tool for understanding the intricate cellular interactions underlying disease progression and therapeutic response. However, existing efforts are hampered by inefficient and error-prone human annotations. Here, we present an experimental and computational approach for automated cell annotation and classification on H&E-stained images. Instead of human annotations, we use multiplexed immunofluorescence (mIF) to define cell types based on cell lineage protein markers. By co-registering H&E images with mIF of the same tissue section at the single-cell level, we create a dataset of 1,127,252 cells with high-quality annotations on tissue microarray cores. A deep learning model combining self-supervised learning with domain adaptation is trained to classify four cell types on H&E images with an overall accuracy of 86%-89%, and the cell classification model is applicable to whole slide images. Further, we show that spatial interactions among specific immune cells in the tumor microenvironment are linked to patient survival and response to immune checkpoint inhibitors. Our work provides a scalable approach for single-cell analysis of standard histopathology and may enable discovery of novel spatial biomarkers for precision oncology.

Suggested Citation

  • Zhe Li & Seyed Hossein Mirjahanmardi & Rasoul Sali & Feyisope Eweje & Matthew Gopaulchan & Leon Kloker & Xiaoming Zhang & Guoxin Li & Yuming Jiang & Ruijiang Li, 2025. "Automated cell annotation and classification on histopathology for spatial biomarker discovery," Nature Communications, Nature, vol. 16(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-61349-1
    DOI: 10.1038/s41467-025-61349-1
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    References listed on IDEAS

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    1. James A. Diao & Jason K. Wang & Wan Fung Chui & Victoria Mountain & Sai Chowdary Gullapally & Ramprakash Srinivasan & Richard N. Mitchell & Benjamin Glass & Sara Hoffman & Sudha K. Rao & Chirag Mahesh, 2021. "Human-interpretable image features derived from densely mapped cancer pathology slides predict diverse molecular phenotypes," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    2. Patricia Switten Nielsen & Jeanette Baehr Georgsen & Mads Sloth Vinding & Lasse Riis Østergaard & Torben Steiniche, 2022. "Computer-Assisted Annotation of Digital H&E/SOX10 Dual Stains Generates High-Performing Convolutional Neural Network for Calculating Tumor Burden in H&E-Stained Cutaneous Melanoma," IJERPH, MDPI, vol. 19(21), pages 1-19, November.
    3. Ramin Nakhli & Katherine Rich & Allen Zhang & Amirali Darbandsari & Elahe Shenasa & Amir Hadjifaradji & Sidney Thiessen & Katy Milne & Steven J. M. Jones & Jessica N. McAlpine & Brad H. Nelson & C. Bl, 2024. "VOLTA: an enVironment-aware cOntrastive ceLl represenTation leArning for histopathology," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
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