Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s Disease

Adult-onset Still’s disease (AOSD) is a complex systemic inflammatory disorder, categorized as an ‘IL-1 driven’ inflammasomapathy. Despite this, the interaction between T and B cells remains poorly understood. We conducted a study, enrolling 7 patients with relapsing AOSD and 15 healthy control subj...

Full description

Bibliographic Details
Main Authors: Valentina Myachikova, Igor Kudryavtsev, Artem Rubinstein, Arthur Aquino, Dmitry Isakov, Alexey Golovkin, Alexey Maslyanskiy
Format: Article
Language:English
Published: MDPI AG 2024-02-01
Series:Current Issues in Molecular Biology
Subjects:
Online Access:https://www.mdpi.com/1467-3045/46/2/75
_version_ 1797298588480438272
author Valentina Myachikova
Igor Kudryavtsev
Artem Rubinstein
Arthur Aquino
Dmitry Isakov
Alexey Golovkin
Alexey Maslyanskiy
author_facet Valentina Myachikova
Igor Kudryavtsev
Artem Rubinstein
Arthur Aquino
Dmitry Isakov
Alexey Golovkin
Alexey Maslyanskiy
author_sort Valentina Myachikova
collection DOAJ
description Adult-onset Still’s disease (AOSD) is a complex systemic inflammatory disorder, categorized as an ‘IL-1 driven’ inflammasomapathy. Despite this, the interaction between T and B cells remains poorly understood. We conducted a study, enrolling 7 patients with relapsing AOSD and 15 healthy control subjects, utilizing deep flow cytometry analysis to examine peripheral blood T- and B-cell subsets. T-cell and B-cell subsets were significantly altered in patients with AOSD. Within CD4+ T cells, Th2 cells were decreased. Additionally, Th17 cell and follicular Th cell subsets were altered within CD45RA–CD62L+ and CD45RA–CD62L– Th cells in patients with AOSD compared to healthy controls. We identified changes in CD8+ T cell maturation and ‘polarization’ in AOSD patients, with an elevated presence of the TEMRA CD8+ T cell subset. Furthermore, the percentage of Tc1 cells was decreased, while the frequency of CCR6–CXCR3– Tc2 cells was elevated. Finally, we determined that the frequency of CD5+CD27– B cells was dramatically decreased in patients with AOSD compared to healthy controls. Further investigations on a large group of patients with AOSD are required to evaluate these adaptive immunity cells in the disease pathogenesis.
first_indexed 2024-03-07T22:38:11Z
format Article
id doaj.art-e83c9a1ddf364f8e9745ee05db004c94
institution Directory Open Access Journal
issn 1467-3037
1467-3045
language English
last_indexed 2024-03-07T22:38:11Z
publishDate 2024-02-01
publisher MDPI AG
record_format Article
series Current Issues in Molecular Biology
spelling doaj.art-e83c9a1ddf364f8e9745ee05db004c942024-02-23T15:12:35ZengMDPI AGCurrent Issues in Molecular Biology1467-30371467-30452024-02-014621177119110.3390/cimb46020075Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s DiseaseValentina Myachikova0Igor Kudryavtsev1Artem Rubinstein2Arthur Aquino3Dmitry Isakov4Alexey Golovkin5Alexey Maslyanskiy6Rheumatology and Immunopathology Research Laboratory, Federal State Budgetary Institution “Almazov National Medical Research Centre” of the Ministry of Health of the Russian Federation, 197341 St. Petersburg, RussiaAutoimmune and Autoinflammatory Diseases Research Laboratory, Federal State Budgetary Institution “Almazov National Medical Research Centre” of the Ministry of Health of the Russian Federation, 197341 St. Petersburg, RussiaAutoimmune and Autoinflammatory Diseases Research Laboratory, Federal State Budgetary Institution “Almazov National Medical Research Centre” of the Ministry of Health of the Russian Federation, 197341 St. Petersburg, RussiaAutoimmune and Autoinflammatory Diseases Research Laboratory, Federal State Budgetary Institution “Almazov National Medical Research Centre” of the Ministry of Health of the Russian Federation, 197341 St. Petersburg, RussiaDepartment of Immunology, First St. Petersburg State Medical University, 197022 St. Petersburg, RussiaAutoimmune and Autoinflammatory Diseases Research Laboratory, Federal State Budgetary Institution “Almazov National Medical Research Centre” of the Ministry of Health of the Russian Federation, 197341 St. Petersburg, RussiaRheumatology and Immunopathology Research Laboratory, Federal State Budgetary Institution “Almazov National Medical Research Centre” of the Ministry of Health of the Russian Federation, 197341 St. Petersburg, RussiaAdult-onset Still’s disease (AOSD) is a complex systemic inflammatory disorder, categorized as an ‘IL-1 driven’ inflammasomapathy. Despite this, the interaction between T and B cells remains poorly understood. We conducted a study, enrolling 7 patients with relapsing AOSD and 15 healthy control subjects, utilizing deep flow cytometry analysis to examine peripheral blood T- and B-cell subsets. T-cell and B-cell subsets were significantly altered in patients with AOSD. Within CD4+ T cells, Th2 cells were decreased. Additionally, Th17 cell and follicular Th cell subsets were altered within CD45RA–CD62L+ and CD45RA–CD62L– Th cells in patients with AOSD compared to healthy controls. We identified changes in CD8+ T cell maturation and ‘polarization’ in AOSD patients, with an elevated presence of the TEMRA CD8+ T cell subset. Furthermore, the percentage of Tc1 cells was decreased, while the frequency of CCR6–CXCR3– Tc2 cells was elevated. Finally, we determined that the frequency of CD5+CD27– B cells was dramatically decreased in patients with AOSD compared to healthy controls. Further investigations on a large group of patients with AOSD are required to evaluate these adaptive immunity cells in the disease pathogenesis.https://www.mdpi.com/1467-3045/46/2/75adult-onset Still’s diseaseAOSDautoinflammation‘IL-1 driven’ diseaseTh cellsCD8+ T cells
spellingShingle Valentina Myachikova
Igor Kudryavtsev
Artem Rubinstein
Arthur Aquino
Dmitry Isakov
Alexey Golovkin
Alexey Maslyanskiy
Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s Disease
Current Issues in Molecular Biology
adult-onset Still’s disease
AOSD
autoinflammation
‘IL-1 driven’ disease
Th cells
CD8+ T cells
title Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s Disease
title_full Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s Disease
title_fullStr Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s Disease
title_full_unstemmed Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s Disease
title_short Deep Immunophenotyping of Circulating T and B Cells in Relapsing Adult-Onset Still’s Disease
title_sort deep immunophenotyping of circulating t and b cells in relapsing adult onset still s disease
topic adult-onset Still’s disease
AOSD
autoinflammation
‘IL-1 driven’ disease
Th cells
CD8+ T cells
url https://www.mdpi.com/1467-3045/46/2/75
work_keys_str_mv AT valentinamyachikova deepimmunophenotypingofcirculatingtandbcellsinrelapsingadultonsetstillsdisease
AT igorkudryavtsev deepimmunophenotypingofcirculatingtandbcellsinrelapsingadultonsetstillsdisease
AT artemrubinstein deepimmunophenotypingofcirculatingtandbcellsinrelapsingadultonsetstillsdisease
AT arthuraquino deepimmunophenotypingofcirculatingtandbcellsinrelapsingadultonsetstillsdisease
AT dmitryisakov deepimmunophenotypingofcirculatingtandbcellsinrelapsingadultonsetstillsdisease
AT alexeygolovkin deepimmunophenotypingofcirculatingtandbcellsinrelapsingadultonsetstillsdisease
AT alexeymaslyanskiy deepimmunophenotypingofcirculatingtandbcellsinrelapsingadultonsetstillsdisease