High-Dimensional Mass Cytometry Reveals Emphysema-associated Changes in the Pulmonary Immune System

• Published in: American journal of respiratory and critical care medicine Vol. 210; no. 8; p. 1002
• Main Authors: Jia, Li, Li, Na, Abdelaal, Tamim R M, Guo, Nannan, Usselsteijn, Marieke E, Van unen, Vincent, Lindelauf, Ciska, Jiang, Qinyue, Xiao, Yanling, Pascutti, M Fernanda, Hiemstra, Pieter S, Koning, Frits, Stolk, Jan, Khedoe, P Padmini
• Format: Journal Article
• Language: English
• Published: New York American Thoracic Society 15.10.2024
• Subjects: Cells; Clinical trials; Emphysema; Flow cytometry; Human subjects
• ISSN: 1073-449X; 1535-4970
• DOI: 10.1164/rccm.202303-0442OCo

Rationale: Chronic inflammation plays an important role in alveolar tissue damage in emphysema, but the underlying immune alterations and cellular interactions are incompletely understood. Objectives: To explore disease-specific pulmonary immune cell alterations and cellular interactions in emphysema. Methods: We used single-cell mass cytometry (CyTOF) to compare the immune compartment in alveolar tissue from 15 patients with severe emphysema and 5 control subjects. Imaging mass cytometry (IMC) was applied to identify altered cell-cell interactions in alveolar tissue from patients with emphysema (n = 12) compared with control subjects (n = 8). Measurements and Main Results: We observed higher percentages of central memory CD4 T cells in combination with lower proportions of effector memory CD4 T cells in emphysema. In addition, proportions of cytotoxic central memory CD8 T cells and CD127+CD27*CD69~ T cells were higher in emphysema, the latter potentially reflecting an influx of circulating lymphocytes into the lungs. Central memory CD8 T cells, isolated from alveolar tissue from patients with emphysema, exhibited an IFN-7 response upon anti-CD3 and anti-CD28 activation. Proportions of CDlc dendritic cells, expressing migratory and costimulatory markers, were higher in emphysema. Importantly, IMC enabled us to visualize increased spatial colocalization of CDlc+ dendritic cells and CD8 T cells in emphysema in situ. Conclusions: Using CyTOF, we characterized the alterations of the immune cell signature in alveolar tissue from patients with chronic obstructive pulmonary disease stage III or IV emphysema versus control lung tissue. These data contribute to a better understanding of the pathogenesis of emphysema and highlight the feasibility of interrogating the immune cell signature using CyTOF and IMC in human lung tissue.