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.

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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

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article

MICRON learns outcome-associated representations of spatial immune microenvironments

Luvna Dhawka, C Chen, Natalie Stanley, Betsy George et al.
bioRxiv (Cold Spring Harbor Laboratory)
Single-cell and spatial transcriptomics
article

MICRON learns outcome-associated representations of spatial immune microenvironments

Luvna Dhawka, C Chen, Natalie Stanley, Betsy George, Baggio Evangelista
article en

Abstract

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.

bioRxiv (Cold Spring Harbor Laboratory)
University of North Carolina at Chapel Hill (US)
National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 23%
Single-cell and spatial transcriptomics
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