Distinct innate and adaptive immunity phenotypic profile at the circulating single-cell level in Psoriatic Arthritis

Copyright © 2023 Elsevier Inc. All rights reserved.

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 253(2023) vom: 01. Aug., Seite 109679
Auteur principal: Fragoulis, George E (Auteur)
Autres auteurs: Vetsika, Eleni-Kyriaki, Kyriakidi, Maria, Verrou, Kleio-Maria, Kollias, George, Tektonidou, Maria G, McInnes, Iain B, Sfikakis, Petros P
Format: Article en ligne
Langue:English
Publié: 2023
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Journal Article Research Support, Non-U.S. Gov't CyTOF Immunophenotyping Mass cytometry Peripheral blood Psoriatic arthritis
Description
Résumé:Copyright © 2023 Elsevier Inc. All rights reserved.
Mass cytometry was employed to investigate 47 circulating leukocyte subsets in patients with active psoriatic arthritis (PsA, n = 16) compared to healthy controls (n = 13), seropositive (RF and/or anti-CCP, n = 12) and seronegative (n = 9) RA patients. Comparing PsA to controls, different cell frequencies were found in both innate and adaptive immunity cell subsets, as well as in cells bridging innate and adaptive immunity. In some T cell subsets increased costimulatory molecules' expression in PsA, was also noted.No changes were observed in patients who remained disease-active after 3 months of treatment, in contrast to those who achieved remission/low-disease activity. Comparing PsA to seropositive RA, elevated frequencies of naïve and activated CD8+ T cells, B cells, MAIT/iNKT and ILCs were found, while the opposite was the case for terminal effector, senescent, and Th2-like cells. Strikingly, the composition of the leukocyte pool in PsA was comparable to seronegative RA, providing evidence for the pathogenetic similarities between these two entities
Description:Date Completed 26.07.2023
Date Revised 26.07.2023
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2023.109679