AI-enabled virtual spatial proteomics from histopathology for interpretable biomarker discovery in lung cancer

Искусственный интеллект для виртуальной пространственной протеомики по данным гистопатологии для интерпретируемого выявления биомаркеров при раке легкого
Zhe Li, Yuchen Li, Jinxi Xiang, Xiyue Wang, Sen Yang, Xiaoming Zhang, Feyisope Eweje, Yijiang M. Chen, Xiangde Luo, Yuanyuan Li, Jonathan Mulholland, Colin P. Bergstrom, Ted Kim, Francesca Olguin, Sierra Hewett, Jeffrey Nirschl, Robert West, Joel W. Neal, Maximilian Diehn, Ruijiang Li, Robert B. West, Yuchen Li, Sierra Willens, Sierra Willens
2026-01-01

H&E to protein expression (HEX)biomarker discoveryhistopathologyimmunotherapy response predictionmultimodal data integrationnon-small-cell lung cancerspatial proteomicstumor-immune nichesvirtual spatial proteomics
Spatial proteomics enables high-resolution mapping of protein expression and can transform our understanding of biology and disease. However, major challenges remain for clinical translation, including cost, complexity and scalability. Here we present H&E to protein expression (HEX), an AI model designed to computationally generate spatial proteomics profiles from standard histopathology slides. Trained and validated on 819,000 histopathology image tiles with matched protein expression from 382 tumor samples, HEX accurately predicts the expression of 40 biomarkers encompassing immune, structural and functional programs. HEX demonstrates substantial performance gains over alternative methods for protein expression prediction from H&E images. We develop a multimodal data integration approach that combines the original H&E image and AI-derived virtual spatial proteomics to enhance outcome prediction. Applied to six independent non-small-cell lung cancer cohorts totaling 2,298 patients, HEX-enabled multimodal integration improved prognostic accuracy by 22% and immunotherapy response prediction by 24-39% compared with conventional clinicopathological and molecular biomarkers. Biological interpretation revealed spatially organized tumor-immune niches predictive of therapeutic response, including the co-localization of T helper cells and cytotoxic T cells in responders, and immunosuppressive tumor-associated macrophage and neutrophil aggregates in non-responders. HEX provides a low-cost and scalable approach to study spatial biology and enables the discovery and clinical translation of interpretable biomarkers for precision medicine.
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A multimodal integration combining H&E images and HEX-derived virtual spatial proteomics improved prognostic accuracy by 22% across six independent non-small-cell lung cancer cohorts (2,298 patients).
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HEX outperforms alternative methods for predicting protein expression from H&E images, showing substantial performance gains.
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HEX was trained/validated on 819,000 image tiles from 382 tumor samples and accurately predicts expression of 40 biomarkers covering immune, structural, and functional programs.
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HEX, an AI model, can computationally generate spatial proteomics profiles from standard H&E histopathology slides.
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HEX-enabled integration improved immunotherapy response prediction by 24–39% versus conventional clinicopathological and molecular biomarkers, and revealed interpretable spatial tumor-immune niches associated with response and resistance.

AI model (HEX) that generates virtual spatial proteomics profiles from H&E histopathology slides

Accuracy and utility of AI-derived virtual spatial proteomics for predicting protein biomarker expression, improving prognostic and immunotherapy response prediction, and enabling interpretable spatial biomarker discovery in non-small-cell lung cancer

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Publication Date
2026-01-01
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Authors
Zhe Li
Yuchen Li
Jinxi Xiang
Xiyue Wang
Sen Yang
Xiaoming Zhang
Feyisope Eweje
Yijiang M. Chen
Xiangde Luo
Yuanyuan Li
Jonathan Mulholland
Colin P. Bergstrom
Ted Kim
Francesca Olguin
Sierra Hewett
Jeffrey Nirschl
Robert West
Joel W. Neal
Maximilian Diehn
Ruijiang Li
Robert B. West
Yuchen Li
Sierra Willens
Sierra Willens
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