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Updated: Nov 7, 2025

Visualization, Quantification, and Mapping of Immune Cell Populations in the Tumor Microenvironment
Published on: March 25, 2020
High Dimensional Imaging Mass Cytometry Panel to Visualize the Tumor Immune Microenvironment Contexture
Roxane Elaldi1,2, Patrice Hemon3, Luciana Petti1
1Université Côte d'Azur, CNRS UMR7275, Institut de Pharmacologie Moléculaire et Cellulaire, Valbonne, France.
Insights
This study introduces a 39-antibody Imaging Mass Cytometry (IMC) panel for detailed analysis of the tumor immune microenvironment (TiME). This tool aids in understanding tumor progression and identifying biomarkers for immunotherapy resistance.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Understanding the tumor immune microenvironment (TiME) is crucial for cancer progression research.
- High-dimensional imaging techniques are needed for comprehensive in situ analysis of TiME.
Purpose of the Study:
- To design and validate a 39-antibody Imaging Mass Cytometry (IMC) panel for human tumor sections.
- To provide an optimized protocol for IMC staining and experimental workflow.
- To enable detailed analysis of TiME components and their interactions.
Main Methods:
- Development of a 39-antibody IMC panel for formalin-fixed paraffin-embedded human tumor tissues.
- Optimization of the staining procedure and experimental workflow for IMC.
- Application of IMC for multiparametric in situ exploration of TiME at a single-cell level.
Main Results:
- The IMC panel successfully deciphers immune cell types and functions within the tumor microenvironment.
- It reveals interactions between immune cells, tumor cells, cancer-associated fibroblasts, nerve fibers, and extracellular matrix proteins.
- The panel allows for the microanatomical mapping of TiME components.
Conclusions:
- The developed IMC panel is a powerful tool for fundamental and clinical cancer research.
- It facilitates the identification of prognostic biomarkers and mechanisms of resistance to immunotherapies.
- This approach enhances the in situ understanding of tumor progression and immune cell dynamics.
Abstract:
The integrative analysis of tumor immune microenvironment (TiME) components, their interactions and their microanatomical distribution is mandatory to better understand tumor progression. Imaging Mass Cytometry (IMC) is a high dimensional tissue imaging system which allows the comprehensive and multiparametric in situ exploration of tumor microenvironments at a single cell level. We describe here the design of a 39-antibody IMC panel for the staining of formalin-fixed paraffin-embedded human tumor sections. We also provide an optimized staining procedure and details of the experimental workflow. This panel deciphers the nature of immune cells, their functions and their interactions with tumor cells and cancer-associated fibroblasts as well as with other TiME structural components known to be associated with tumor progression like nerve fibers and tumor extracellular matrix proteins. This panel represents a valuable innovative and powerful tool for fundamental and clinical studies that could be used for the identification of prognostic biomarkers and mechanisms of resistance to current immunotherapies.
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