4.7 Review

Clinical and research applications of multiplexed immunohistochemistry and in situ hybridization

Journal

JOURNAL OF PATHOLOGY
Volume 254, Issue 4, Pages 405-417

Publisher

WILEY
DOI: 10.1002/path.5663

Keywords

multiplex in situ hybridization; multiplex immunohistochemistry; single‐ cell transcriptomes; spatial transcriptomics; surrogate end‐ points

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Novel multiplexing technologies for tissues have greatly impacted basic and translational research by allowing highly multiplexed immunohistochemistry or in situ RNA measurements with objective biomarker quantification and increased sensitivity. These technologies offer unprecedented insights into tissue biology and biomarker science, but implementation requires extensive time and resources.
Over the past decade, invention and adoption of novel multiplexing technologies for tissues have made increasing impacts in basic and translational research and, to a lesser degree, clinical medicine. Platforms capable of highly multiplexed immunohistochemistry or in situ RNA measurements promise evaluation of protein or RNA targets at levels of plex and sensitivity logs above traditional methods - all with preservation of spatial context. These methods promise objective biomarker quantification, markedly increased sensitivity, and single-cell resolution. Increasingly, development of novel technologies is enabling multi-omic interrogations with spatial correlation of RNA and protein expression profiles in the same sample. Such sophisticated methods will provide unprecedented insights into tissue biology, biomarker science, and, ultimately, patient health. However, this sophistication comes at significant cost, requiring extensive time, practical knowledge, and resources to implement. This review will describe the technical features, advantages, and limitations of currently available multiplexed immunohistochemistry and spatial transcriptomic platforms. (c) 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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