Circulating immunome fingerprint in eosinophilic esophagitis is associated with clinical response to proton pump inhibitor treatment

• Published in: Frontiers in immunology Vol. 15; p. 1374611
• Main Authors: Ugalde-Triviño, Lola, Molina-Jiménez, Francisca, H-Vázquez, Juan, Relaño-Rupérez, Carlos, Arias-González, Laura, Casabona, Sergio, Pérez-Fernández, María Teresa, Martín-Domínguez, Verónica, Fernández-Pacheco, Jennifer, Lucendo, Alfredo J., Bernardo, David, Santander, Cecilio, Majano, Pedro
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 2024
• Subjects: Adult; biomarker; Biomarkers - blood; Biopsy; Case-Control Studies; Dendritic Cells - immunology; eosinophilic esophagitis; Eosinophilic Esophagitis - blood; Eosinophilic Esophagitis - diagnosis; Eosinophilic Esophagitis - drug therapy; Eosinophilic Esophagitis - immunology; Eosinophils - immunology; Female; Humans; immunome; Male; Middle Aged; plasmacytoid dendritic cells; Proton Pump Inhibitors - therapeutic use; spectral cytometry; Treatment Outcome; Young Adult; immunome; plasmacytoid dendritic cells; biomarker; spectral cytometry; eosinophilic esophagitis
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2024.1374611

The aim of the study was to characterize the circulating immunome of patients with EoE before and after proton pump inhibitor (PPI) treatment in order to identify potential non-invasive biomarkers of treatment response. PBMCs from 19 healthy controls and 24 EoE patients were studied using a 39-plex spectral cytometry panel. The plasmacytoid dendritic cell (pDC) population was differentially characterized by spectral cytometry analysis and immunofluorescence assays in esophageal biopsies from 7 healthy controls and 13 EoE patients. Interestingly, EoE patients at baseline had lower levels of circulating pDC compared with controls. Before treatment, patients with EoE who responded to PPI therapy had higher levels of circulating pDC and classical monocytes, compared with non-responders. Moreover, following PPI therapy pDC levels were increased in all EoE patients, while normal levels were only restored in PPI-responding patients. Finally, circulating pDC levels inversely correlated with peak eosinophil count and pDC count in esophageal biopsies. The number of tissue pDCs significantly increased during active EoE, being even higher in non-responder patients when compared to responder patients pre-PPI. pDC levels decreased after PPI intake, being further restored almost to control levels in responder patients post-PPI. We hereby describe a unique immune fingerprint of EoE patients at diagnosis. Moreover, circulating pDC may be also used as a novel non-invasive biomarker to predict subsequent response to PPI treatment.