<p>Spatial proteomics technologies have transformed our understanding of complex tissue architecture in cancer but present unique challenges for computational analysis<sup><CitationRef CitationID="CR1">1</CitationRef></sup>. Each study uses a different marker panel and protocol, and most methods are tailored to single cohorts, which limits knowledge transfer and robust biomarker discovery. Here we present Virtual Tissues (VirTues), a general-purpose foundation model for spatial proteomics that learns marker-aware, multi-scale representations of proteins, cells, niches and tissues directly from multiplex imaging data. From a single pretrained backbone, VirTues supports marker reconstruction, cell segmentation and typing, niche annotation, spatial biomarker discovery and patient stratification, including zero-shot annotation across heterogeneous panels and datasets. In triple-negative breast cancer, VirTues-derived biomarkers predict anti-PD-L1 chemo-immunotherapy response<sup><CitationRef CitationID="CR2">2</CitationRef></sup> and stratify disease-free survival in an independent cohort<sup><CitationRef CitationID="CR3">3</CitationRef></sup>, outperforming state-of-the-art biomarkers derived from the same datasets and current clinical stratification schemes.</p>

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The Virtual Tissues foundation model resolves spatial proteomics across scales

  • Johann Wenckstern,
  • Eeshaan Jain,
  • Benedikt von Querfurth,
  • Yexiang Cheng,
  • Kiril Vasilev,
  • Matteo Pariset,
  • Phil F. Cheng,
  • Petros Liakopoulos,
  • Olivier Michielin,
  • Andreas Wicki,
  • Gabriele Gut,
  • Charlotte Bunne

摘要

Spatial proteomics technologies have transformed our understanding of complex tissue architecture in cancer but present unique challenges for computational analysis1. Each study uses a different marker panel and protocol, and most methods are tailored to single cohorts, which limits knowledge transfer and robust biomarker discovery. Here we present Virtual Tissues (VirTues), a general-purpose foundation model for spatial proteomics that learns marker-aware, multi-scale representations of proteins, cells, niches and tissues directly from multiplex imaging data. From a single pretrained backbone, VirTues supports marker reconstruction, cell segmentation and typing, niche annotation, spatial biomarker discovery and patient stratification, including zero-shot annotation across heterogeneous panels and datasets. In triple-negative breast cancer, VirTues-derived biomarkers predict anti-PD-L1 chemo-immunotherapy response2 and stratify disease-free survival in an independent cohort3, outperforming state-of-the-art biomarkers derived from the same datasets and current clinical stratification schemes.