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Updated: Jul 30, 2025

A Rapid Method for Multispectral Fluorescence Imaging of Frozen Tissue Sections
Published on: March 30, 2020
Seven-colour multiplex immunochemistry/immunofluorescence and whole slide imaging of frozen sections
Saem Mul Park1, Chun-Jen J Chen2, Joanna E Mathy1
1School of Biological Sciences, University of Auckland, Auckland, New Zealand; Maurice Wilkins Centre, University of Auckland, Auckland, New Zealand.
Insights
We developed a novel multiplex immunochemistry/immunofluorescence (mIHC/IF) workflow for simultaneous detection of seven markers in frozen tissue sections. This method efficiently reveals tumor-immune complexity for immuno-oncology research.
Area of Science:
- Biomedical Imaging
- Immunohistochemistry
- Immunofluorescence
Background:
- Multiplex immunochemistry/immunofluorescence (mIHC/IF) is crucial for analyzing the tumor microenvironment (TME) in immuno-oncology.
- Traditional mIHC/IF methods often require sequential staining and are incompatible with frozen tissue sections.
- Advancements allow more markers but often lack frozen section compatibility.
Purpose of the Study:
- To establish a simple mIHC/IF workflow for simultaneous staining of multiple biomarkers in frozen tissue sections.
- To enable high-throughput analysis of tumor-immune complexity using automated slide scanning and digital quantification.
- To provide a versatile tool for translational research requiring frozen tissue analysis.
Main Methods:
- Developed a novel mIHC/IF workflow using fluorophore-conjugated antibodies for simultaneous staining.
- Enabled detection of seven markers in a single frozen tissue section.
- Integrated automated whole slide imaging and computational image analysis for quantification of cellular populations and spatial interactions.
Main Results:
- Successfully visualized seven markers simultaneously in frozen tissue sections.
- Efficiently revealed the complexity of the tumor-immune microenvironment in metastatic melanoma.
- Quantified immune and stromal cell populations and their spatial relationships within the TME.
- Demonstrated the workflow's compatibility with both direct (fluorophore-conjugated) and indirect (primary/secondary antibody) labeling.
Conclusions:
- The new mIHC/IF workflow enables simultaneous detection of seven markers in frozen sections.
- This method provides efficient, high-quality data for immuno-oncology and translational studies.
- The workflow is valuable for applications requiring frozen sections, such as spatial transcriptomics.
Abstract:
Multiplex Immunochemistry/Immunofluorescence (mIHC/IF) aims to visualise multiple biomarkers in a single tissue section and is especially powerful when used on slide scanners coupled with digital analysis tools. mIHC/IF is commonly employed in immuno-oncology to characterise features of the tumour microenvironment (TME) and correlate them with clinical parameters to guide prognostication and therapy. However, mIHC/IF can be applied to a wide range of organisms in any physiological or disease context. Recent innovation has extended the number of markers that can be detected using slide scanners well beyond the 3-4 markers typically reported in traditional fluorescence microscopy. However, these methods often require sequential antibody staining and stripping, and are not compatible with frozen tissue sections. Using fluorophore-conjugated antibodies, we have established a simple mIHC/IF imaging workflow that enables simultaneous staining and detection of seven markers in a single section of frozen tissue. Coupled with automated whole slide imaging and digital quantification, our data efficiently revealed the tumour-immune complexity in metastatic melanoma. Computational image analysis quantified the immune and stromal cell populations present in the TME as well as their spatial interactions. This imaging workflow can also be performed with an indirect labelling panel consisting of primary and secondary antibodies. Our new methods, combined with digital quantification, will provide a valuable tool for high-quality mIHC/IF assays in immuno-oncology research and other translational studies, especially in circumstances where frozen sections are required for detection of particular markers, or for applications where frozen sections may be preferred, such as spatial transcriptomics.
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