ArticleMolecular & cellular proteomics : MCP2026
mosna Reveals Different Types of Cellular Interactions Predictive of Response to Immunotherapies and Survival in Cancer.
Article in Molecular & cellular proteomics : MCP, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed.
- Organ-Specific Migration License (OSML) theory: a novel paradigm for spatiotemporal regulation and intervention of cross-organ immune cell migration in tumor immune responses.Cell communication and signaling : CCS · 2026Review
- Modeling macrophage-T cell interactions in the breast cancer immune microenvironment: from spatial omics to functional validation.Frontiers in immunology · 2026Review
- Spatial proteomics of the tumor microenvironment in melanoma: current insights and future directions.Frontiers in immunology · 2025Review
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Abstract
Spatially resolved omics enable the discovery of tissue organization of biological or clinical importance. Despite the existence of several methods, performing a rational analysis, including multiple algorithms while integrating different conditions such as clinical data, is still not trivial. To make such investigations more accessible, we developed mosna, a Python package to analyze spatial omics data in integration with clinical or biological data, providing insight into cell interaction patterns or tissue architecture. mosna is compatible with all spatial omics techniques, leverages tysserand to build accurate spatial networks, and is compatible with Squidpy. It proposes an analysis pipeline in which increasingly complex features computed at each step with either the mosna-algorithms or others can be explored in integration with clinical data. The approach produces easy-to-use descriptive statistics and data visualization while seamlessly training machine learning models and identifying variables with the most predictive power. mosna can take as input any dataset produced by spatial omics methods, including sub-cellular resolved transcriptomics (MERFISH, seqFISH, and Xenium) and proteomics (CODEX, MIBI-TOF, and low-plex immuno-fluorescence) as well as spot-based spatial transcriptomics (10x Visium, Slide-seq, and Stereo-seq). Integration with experimental metadata or clinical data is adapted to binary conditions, such as biological treatments or response status of patients, and to survival data. We demonstrate the proposed analysis pipeline on two spatially resolved proteomic datasets and a spatial transcriptomics dataset containing either binary response to immunotherapy or survival data, and we assess the performance of the proposed niche discovering method in a manually annotated spatial transcriptomic dataset. mosna identifies features describing cellular composition and spatial patterns that can provide biological insight regarding factors that affect response to immunotherapies or survival. mosna is made publicly available to the community, together with relevant documentation at https://mosna-documentation.readthedocs.io/en/latest/index.html and tutorials implemented as Jupyter notebooks to reproduce the result at https://github.com/AlexCoul/mosna.
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