Seven-colour multiplex immunochemistry/immunofluorescence and whole slide imaging of frozen sections.


Journal

Journal of immunological methods
ISSN: 1872-7905
Titre abrégé: J Immunol Methods
Pays: Netherlands
ID NLM: 1305440

Informations de publication

Date de publication:
07 2023
Historique:
received: 03 04 2023
revised: 09 05 2023
accepted: 09 05 2023
medline: 13 6 2023
pubmed: 13 5 2023
entrez: 12 5 2023
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 37172777
pii: S0022-1759(23)00072-8
doi: 10.1016/j.jim.2023.113490
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Antibodies 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

113490

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no potential conflicts of interest.

Auteurs

Saem Mul Park (SM)

School of Biological Sciences, University of Auckland, Auckland, New Zealand; Maurice Wilkins Centre, University of Auckland, Auckland, New Zealand.

Chun-Jen J Chen (CJ)

School of Biological Sciences, University of Auckland, Auckland, New Zealand.

Joanna E Mathy (JE)

School of Biological Sciences, University of Auckland, Auckland, New Zealand; Maurice Wilkins Centre, University of Auckland, Auckland, New Zealand.

Shelly C Y Lin (SCY)

School of Biological Sciences, University of Auckland, Auckland, New Zealand; Maurice Wilkins Centre, University of Auckland, Auckland, New Zealand.

Richard C W Martin (RCW)

Department of Surgery, Te Whatu Ora Waitemata Auckland, New Zealand.

Jon A Mathy (JA)

Department of Surgery, Faculty of Medical Health Sciences, Waipapa Taumata Rau - The University of Auckland, Auckland, New Zealand; Auckland Regional Plastic, Reconstructive & Hand Surgery Unit, Auckland, New Zealand.

James H F Shaw (JHF)

Oncology Surgery Ltd, Auckland, New Zealand. Electronic address: shawjhf@xtra.co.nz.

P Rod Dunbar (PR)

School of Biological Sciences, University of Auckland, Auckland, New Zealand; Maurice Wilkins Centre, University of Auckland, Auckland, New Zealand. Electronic address: r.dunbar@auckland.ac.nz.

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Classifications MeSH