Joint Modeling of Spatial Dependencies Across Multiple Subjects in Multiplexed Tissue Imaging
The tumor microenvironment (TME) is a spatially heterogeneous ecosystem where cellular interactions shape tumor progression and response to therapy. Multiplexed imaging technologies enable high-resolution spatial characterization of the TME, yet statistical methods for analyzing multi-subject spatia...
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Main Authors | , , , |
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Format | Journal Article |
Language | English |
Published |
03.04.2025
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Subjects | |
Online Access | Get full text |
DOI | 10.48550/arxiv.2504.02693 |
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Summary: | The tumor microenvironment (TME) is a spatially heterogeneous ecosystem where
cellular interactions shape tumor progression and response to therapy.
Multiplexed imaging technologies enable high-resolution spatial
characterization of the TME, yet statistical methods for analyzing
multi-subject spatial tissue data remain limited. We propose a Bayesian
hierarchical model for inferring spatial dependencies in multiplexed imaging
datasets across multiple subjects. Our model represents the TME as a
multivariate log-Gaussian Cox process, where spatial intensity functions of
different cell types are governed by a latent multivariate Gaussian process. By
pooling information across subjects, we estimate spatial correlation functions
that capture within-type and cross-type dependencies, enabling interpretable
inference about disease-specific cellular organization. We validate our method
using simulations, demonstrating robustness to latent factor specification and
spatial resolution. We apply our approach to two multiplexed imaging datasets:
pancreatic cancer and colorectal cancer, revealing distinct spatial
organization patterns across disease subtypes and highlighting tumor-immune
interactions that differentiate immune-permissive and immune-exclusive
microenvironments. These findings provide insight into mechanisms of immune
evasion and may inform novel therapeutic strategies. Our approach offers a
principled framework for modeling spatial dependencies in multi-subject data,
with broader applicability to spatially resolved omics and imaging studies. An
R package, available online, implements our methods. |
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DOI: | 10.48550/arxiv.2504.02693 |