{"title":"Immunophenotypic Profiling Reveals Circulating Lymphocyte Dysregulation in Primary Sjögren's Syndrome","authors":"Xianghui Wen, Yanli Zhang, Xinyu Wu, Xuqi Zheng, Mingcan Yang, Dong Liu, Budian Liu, Qiujing Wei, Xiehui Chen, Peng Zhang, Jieruo Gu","doi":"10.1111/1756-185X.70276","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objectives</h3>\n \n <p>To investigate peripheral T and B cell subset alterations in primary Sjögren's syndrome (pSS) and their associations with disease activity (ESSDAI).</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>This study enrolled 43 patients with pSS and 46 healthy controls (HCs). Demographic data and clinical manifestations were collected for all participants. Flow cytometry was utilized to detect the frequencies of T and B cell subsets in peripheral blood mononuclear cells.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Primary Sjögren's syndrome patients exhibited elevated naïve CD4+ T cells, central memory CD4+ T cells, virus-specific CD8+ T cells, Th2/Th17 cells, total B cells, and CD21−/low B cells. Conversely, terminally differentiated/exhausted CD4+ T cells, Th1/Tc1 cells, and plasma cells were reduced. ESSDAI correlated positively with Tc cells and CD21−/low B cells and inversely with plasma cells.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>T and B cell dysregulation may drive immune dysfunction in pSS, with specific subsets linked to disease severity.</p>\n </section>\n </div>","PeriodicalId":14330,"journal":{"name":"International Journal of Rheumatic Diseases","volume":"28 6","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Rheumatic Diseases","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1756-185X.70276","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
To investigate peripheral T and B cell subset alterations in primary Sjögren's syndrome (pSS) and their associations with disease activity (ESSDAI).
Methods
This study enrolled 43 patients with pSS and 46 healthy controls (HCs). Demographic data and clinical manifestations were collected for all participants. Flow cytometry was utilized to detect the frequencies of T and B cell subsets in peripheral blood mononuclear cells.
Results
Primary Sjögren's syndrome patients exhibited elevated naïve CD4+ T cells, central memory CD4+ T cells, virus-specific CD8+ T cells, Th2/Th17 cells, total B cells, and CD21−/low B cells. Conversely, terminally differentiated/exhausted CD4+ T cells, Th1/Tc1 cells, and plasma cells were reduced. ESSDAI correlated positively with Tc cells and CD21−/low B cells and inversely with plasma cells.
Conclusions
T and B cell dysregulation may drive immune dysfunction in pSS, with specific subsets linked to disease severity.
期刊介绍:
The International Journal of Rheumatic Diseases (formerly APLAR Journal of Rheumatology) is the official journal of the Asia Pacific League of Associations for Rheumatology. The Journal accepts original articles on clinical or experimental research pertinent to the rheumatic diseases, work on connective tissue diseases and other immune and allergic disorders. The acceptance criteria for all papers are the quality and originality of the research and its significance to our readership. Except where otherwise stated, manuscripts are peer reviewed by two anonymous reviewers and the Editor.