Machine learning assisted immune profiling of COPD identifies a unique emphysema subtype independent of GOLD stage
Natalie Bordag,
Katharina Jandl,
Ayu Hutami Syarif,
Jürgen Gindlhuber,
Diana Schnoegl,
Ayse Ceren Mutgan,
Vasile Foris,
Konrad Hoetzenecker,
Panja Maria Boehm,
Robab Breyer-Kohansal,
Katarina Zeder,
Gregor Gorkiewicz,
Francesca Polverino,
Slaven Crnkovic,
Grazyna Kwapiszewska,
Leigh Matthew Marsh
Affiliations
Natalie Bordag
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Department of Dermatology and Venereology, Medical University of Graz, Graz, Styria 8010, Austria
Katharina Jandl
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Division of Pharmacology, Otto Loewi Research Centre, Graz, Styria 8010, Austria
Ayu Hutami Syarif
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Otto Loewi Research Centre, Lung Research Cluster, Medical University of Graz, Graz, Styria 8010, Austria
Jürgen Gindlhuber
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Otto Loewi Research Centre, Lung Research Cluster, Medical University of Graz, Graz, Styria 8010, Austria
Diana Schnoegl
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria
Ayse Ceren Mutgan
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Otto Loewi Research Centre, Lung Research Cluster, Medical University of Graz, Graz, Styria 8010, Austria
Vasile Foris
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA; Harvard Medical School, Boston, MA 02115, USA; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Styria 8010, Austria
Konrad Hoetzenecker
Department of Thoracic Surgery, Medical University of Vienna, Vienna, Vienna 1090, Austria
Panja Maria Boehm
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Department of Thoracic Surgery, Medical University of Vienna, Vienna, Vienna 1090, Austria
Robab Breyer-Kohansal
Ludwig Boltzmann Institute for Lung Health, Vienna, Vienna 1140, Austria; Department of Respiratory and Pulmonary Diseases, Vienna Healthcare Group, Clinic Hietzing, Vienna, Vienna 1090, Austria
Katarina Zeder
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Styria 8010, Austria; University of Maryland, Institute of Health Computing, Bethesda, MD 20852, USA
Gregor Gorkiewicz
Diagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Styria 8010, Austria
Francesca Polverino
Baylor College of Medicine, Department of Medicine, Houston, TX 77030, USA
Slaven Crnkovic
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Otto Loewi Research Centre, Lung Research Cluster, Medical University of Graz, Graz, Styria 8010, Austria; Institute for Lung Health, Cardiopulmonary Institute, Member of the German Center for Lung Research, Justus-Liebig University Giessen, 35392 Giessen, Germany
Grazyna Kwapiszewska
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Otto Loewi Research Centre, Lung Research Cluster, Medical University of Graz, Graz, Styria 8010, Austria; Institute for Lung Health, Cardiopulmonary Institute, Member of the German Center for Lung Research, Justus-Liebig University Giessen, 35392 Giessen, Germany
Leigh Matthew Marsh
Ludwig Boltzmann Institute for Lung Vascular Research, Graz, Styria 8010, Austria; Otto Loewi Research Centre, Lung Research Cluster, Medical University of Graz, Graz, Styria 8010, Austria; Corresponding author
Summary: Chronic obstructive pulmonary disease (COPD) is a severe, progressive, and heterogeneous disease with a poor outcome. Inflammation plays a central role in disease pathogenesis; however, the interplay between immune changes and disease heterogeneity has been difficult to unravel. We performed a multilevel immunoinflammatory characterization of patients with COPD using flow cytometry, cytokine profiling, single-cell, or spatial transcriptomics in combination with machine learning algorithms. Our cross-cohort analysis demonstrated shared skewing of immune profiles in COPD lungs toward adaptive immune cells. We furthermore identified a subgroup of patients with COPD with a distinct immune profile, characterized by increased antigen-presenting cells, mast cells, and CD8+ cells, and circulating IL-1β, IFN-β, and GM-CSF, that were associated with increased emphysema severity and decreased gas exchange parameters independent of their GOLD-stage. Our findings suggest that unbiased immune profiling can refine disease classification and reveal inflammation-driven disease subtypes with potential relevance for prognosis and treatment strategies.