4.4 Article

Lymphocyte subpopulations in Sjogren's syndrome are distinct in anti-SSA-positive patients and related to disease activity

期刊

CLINICAL RHEUMATOLOGY
卷 40, 期 7, 页码 2791-2804

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SPRINGER LONDON LTD
DOI: 10.1007/s10067-020-05537-y

关键词

B lymphocytes; Disease activity; Sjogren's syndrome; SSA; T lymphocytes

资金

  1. Academia Cuf/Jose de Mello Saude, Carnaxide, Portugal
  2. Sociedade Portuguesa de Reumatologia, Lisbon, Portugal

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In Sjogren's syndrome, a distinctive lymphocyte subset distribution profile seems to be associated with positive anti-SSA antibody. Specifically, SSA+SjS patients show increased percentages of IL-21(+)CD4(+) and CD8(+) T cells, suggesting their potential involvement in disease pathogenesis and activity, and their utility for prognosis and assessment of response to therapy.
Objectives Sjogren's syndrome (SjS) patients exhibit great phenotypical heterogeneity, reinforced by the positiveness of anti-SSA antibody. We aimed to evaluate lymphocyte subpopulations in SSA-positive (SSA+SjS) and SSA-negative (SSA-SjS) SjS patients, Sicca patients, and healthy controls (HC), and to investigate associations between lymphocyte subpopulations and disease activity in SjS. Methods According to the fulfilment of the ACR/EULAR 2016 classification criteria, patients were included as SjS or as Sicca. HC were selected from the Ophthalmology outpatient clinic. Lymphocyte subpopulations were characterized by flow cytometry. Statistical analysis was performed with GraphPad Prism(TM), with statistical significance concluded if p < 0.05. Results We included 53 SjS patients (38 SSA+ and 15 SSA-), 72 Sicca, and 24 HC. SSA+SjS patients presented increased IL-21(+)CD4(+) and CD8(+) T cells compared to Sicca and HC, whereas compared to SSA-SjS patients, only IL-21(+)CD4(+) T cell percentages were increased and Tfh17 percentages and numbers were decreased. Compared to Sicca and HC, SSA+SjS patients had higher levels of CD24(Hi)CD38(Hi) B cells, naive B cells, and IgM(-/+)CD38(++) plasmablasts, and lower levels of memory B cells, including CD24(Hi)CD27(+) B cells. SSA+SjS patients with clinically active disease had positive correlations between ESSDAI and IL-21(+)CD4(+) (p = 0.038, r = 0.456) and IL-21(+)CD8(+) T cells (p = 0.046, r = 0.451). Conclusions In SjS, a distinct lymphocyte subset distribution profile seems to be associated with positive anti-SSA. Moreover, the association between ESSDAI and IL-21(+)CD4(+) and IL-21(+)CD8(+) (follicular) T cells in SSA+SjS patients suggests the involvement of these cells in disease pathogenesis and activity, and possibly their utility for the prognosis and assessment of response to therapy.

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