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

被引:0
|
作者
Park, Saem Mul [1 ,2 ]
Chen, Chun-Jen J. [1 ]
Mathy, Joanna E. [1 ,2 ]
Lin, Shelly C. Y. [1 ,2 ]
Martin, Richard C. W. [3 ]
Mathy, Jon A. [4 ,5 ]
Shaw, James H. F. [6 ]
Dunbar, P. Rod [1 ,2 ]
机构
[1] Univ Auckland, Sch Biol Sci, 3a Symonds St,Private Bag 92019, Auckland 1142, New Zealand
[2] Univ Auckland, Maurice Wilkins Ctr, Auckland, New Zealand
[3] Te Whatu Ora Waitemata Auckland, Dept Surg, Auckland, New Zealand
[4] The Univ Auckland, Waipapa Taumata Rau, Fac Med Hlth Sci, Dept Surg, Auckland, New Zealand
[5] Auckland Reg Plast, Reconstruct & Hand Surg Unit, Auckland, New Zealand
[6] Oncol Surg Ltd, Auckland, New Zealand
关键词
Multiplex immunochemistry; Multiplex immunofluorescence; Digital pathology; IMMUNOHISTOCHEMISTRY; CELLS;
D O I
10.1016/j.jim.2023.113490
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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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页数:8
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