Single-cell spatial landscapes of the lung tumour immune microenvironment

Mark Sorin(McGill University), Morteza Rezanejad(University of Toronto), Elham Karimi(McGill University), Benoit Fiset(McGill University), Lysanne Desharnais(McGill University), Lucas J. M. Perus(McGill University), Simon Milette(McGill University), Miranda W. Yu(McGill University), Sarah M. Maritan(McGill University), Samuel Doré(McGill University), Émilie Pichette(McGill University Health Centre), William Enlow(Institut universitaire de cardiologie et de pneumologie de Québec), Andréanne Gagné(Institut universitaire de cardiologie et de pneumologie de Québec), Yuhong Wei(McGill University), Michèle Orain(Institut universitaire de cardiologie et de pneumologie de Québec), Venkata Manem(Innovation and Economic Development Trois Rivières), Roni Rayes(McGill University), Peter M. Siegel(McGill University), Sophie Camilleri‐Broët(McGill University), Pierre Fiset(McGill University), Patrice Desmeules(Institut universitaire de cardiologie et de pneumologie de Québec), Jonathan Spicer(McGill University Health Centre), Daniela F. Quail(McGill University Health Centre), Philippe Joubert(Institut universitaire de cardiologie et de pneumologie de Québec), Logan A. Walsh(McGill Genome Centre)
Nature
February 1, 2023
Cited by 372Open Access
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Abstract

Abstract Single-cell technologies have revealed the complexity of the tumour immune microenvironment with unparalleled resolution 1–9 . Most clinical strategies rely on histopathological stratification of tumour subtypes, yet the spatial context of single-cell phenotypes within these stratified subgroups is poorly understood. Here we apply imaging mass cytometry to characterize the tumour and immunological landscape of samples from 416 patients with lung adenocarcinoma across five histological patterns. We resolve more than 1.6 million cells, enabling spatial analysis of immune lineages and activation states with distinct clinical correlates, including survival. Using deep learning, we can predict with high accuracy those patients who will progress after surgery using a single 1-mm 2 tumour core, which could be informative for clinical management following surgical resection. Our dataset represents a valuable resource for the non-small cell lung cancer research community and exemplifies the utility of spatial resolution within single-cell analyses. This study also highlights how artificial intelligence can improve our understanding of microenvironmental features that underlie cancer progression and may influence future clinical practice.


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