MICRON learns outcome-associated representations of spatial immune microenvironments
Spatial imaging proteomics modalities, such as imaging mass cytometry, enable comprehensive identification of immune microenvironments driving disease outcomes. Identifying outcome-associated immune microenvironments from these data has proven to be complex, as it requires segmenting cells with complex shapes and reconciling spatial signatures across many heterogeneous samples. We present MICRON, a segmentation-free, fully automated multiple-instance learning based tool for automatic identification of outcome-linked immune microenvironments. MICRON learns representations of samples profiled with spatial imaging proteomics modalities, enabling more accurate prognostic and diagnostic prediction over existing approaches. As a case study, we show that MICRON generates a comprehensive importance map that reveals key outcome-associated immune microenvironments in brain cancer, uncovering coordinated cell-cell communication between astrocytes, NK cells, and macrophages linked to survival outcomes. MICRON is provided as open source software for broad use by clinicians and biologists at https://github.com/ChenCookie/micron.
Authors
- Luvna Dhawka (ORCID: https://orcid.org/0000-0001-7666-3060)
- C Chen
- Natalie Stanley (ORCID: https://orcid.org/0009-0006-8686-1638)
- Betsy George
- Baggio Evangelista
Institutions
- University of North Carolina at Chapel Hill (US)
Publication Details
- Journal
- bioRxiv (Cold Spring Harbor Laboratory)
- Published
- 2026-04-16
- DOI
- https://doi.org/10.64898/2026.04.14.718488
- Primary Topic
- Single-cell and spatial transcriptomics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Institute of Allergy and Infectious Diseases