Author
Listed:
- Mark Sorin
(McGill University
McGill University)
- Morteza Rezanejad
(University of Toronto
University of Toronto)
- Elham Karimi
(McGill University)
- Benoit Fiset
(McGill University)
- Lysanne Desharnais
(McGill University
McGill University)
- Lucas J. M. Perus
(McGill University
McGill University)
- Simon Milette
(McGill University
McGill University)
- Miranda W. Yu
(McGill University
McGill University)
- Sarah M. Maritan
(McGill University
McGill University)
- Samuel Doré
(McGill University
McGill University)
- Émilie Pichette
(McGill University)
- William Enlow
(Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University)
- Andréanne Gagné
(Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University)
- Yuhong Wei
(McGill University)
- Michele Orain
(Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University)
- Venkata S. K. Manem
(Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University
University of Quebec at Trois-Rivières)
- Roni Rayes
(McGill University)
- Peter M. Siegel
(McGill University
McGill University
McGill University)
- Sophie Camilleri-Broët
(McGill University)
- Pierre Olivier Fiset
(McGill University)
- Patrice Desmeules
(Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University)
- Jonathan D. Spicer
(McGill University
McGill University
McGill University Health Center)
- Daniela F. Quail
(McGill University
McGill University
McGill University)
- Philippe Joubert
(Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University)
- Logan A. Walsh
(McGill University
McGill University)
Abstract
Single-cell technologies have revealed the complexity of the tumour immune microenvironment with unparalleled resolution1–9. 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-mm2 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.
Suggested Citation
Mark Sorin & Morteza Rezanejad & Elham Karimi & Benoit Fiset & Lysanne Desharnais & Lucas J. M. Perus & Simon Milette & Miranda W. Yu & Sarah M. Maritan & Samuel Doré & Émilie Pichette & William Enlow, 2023.
"Single-cell spatial landscapes of the lung tumour immune microenvironment,"
Nature, Nature, vol. 614(7948), pages 548-554, February.
Handle:
RePEc:nat:nature:v:614:y:2023:i:7948:d:10.1038_s41586-022-05672-3
DOI: 10.1038/s41586-022-05672-3
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