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.

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