Abstract

BackgroundTo understand the relationship between regulatory B cells (Bregs) and juvenile idiopathic arthritis (JIA), we analyzed the percentages of Bregs and their function in peripheral blood (PB) and synovial fluid (SF) of JIA patients.MethodsTwenty-one JIA patients and 11 children with growing pain but without known rheumatic diseases as controls were included. The B cell phenotype and intracellular production of IL-10 of Bregs were assessed by flow cytometry. Mononuclear cells from PB and SF were stimulated to produce IL-10 in vitro for the identification of IL-10- producing regulatory B cells.ResultsThe percentage of CD24hiCD38hi Bregs in the PB of JIA patients was significantly decreased compared to that in controls, and it was even lower in the SF of JIA patients compared to that in the PB. CD24hiCD38hi Bregs frequency was significantly lower in the PB of RF-positive patients than in RF-negative patients. Frequency of IL-10-producing regulatory B cells (B10 cells) was significantly lower in active JIA patients than that in inactive patients.ConclusionsThe inability of the host to produce enough regulatory B cells in PB and especially in SF of JIA patients may contribute to the disease, especially the local inflammation.

Highlights

  • To understand the relationship between regulatory B cells (Bregs) and juvenile idiopathic arthritis (JIA), we analyzed the percentages of Regulatory B cells (Bregs) and their function in peripheral blood (PB) and synovial fluid (SF) of JIA patients

  • Peripheral blood and synovial fluid mononuclear cells from subjects were phenotypically analyzed by flow cytometry for their expression of CD19, CD24, and CD38 surface markers

  • B10 cells levels Since B10 cells are a specific subgroup of Bregs, we examined whether there was a correlation between the level of CD24hiCD38hi Bregs and the level of B10 cells in JIA patients

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Summary

Introduction

To understand the relationship between regulatory B cells (Bregs) and juvenile idiopathic arthritis (JIA), we analyzed the percentages of Bregs and their function in peripheral blood (PB) and synovial fluid (SF) of JIA patients. Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatic disease in children [1]. International League of Associations for Rheumatology (ILAR) has classified it into 7 subtypes by the number of joints and the type of extra-articular involvement [2]. Children with JIA are at risk for joint damage, resulting in poor functional outcomes and decreased quality of life [3]. Recent studies have suggested that B cells may have a role in these disorders. B cell-related genes were up-regulated in JIA patients [4], and memory B cells were increased in oligoarticular and polyarticular JIA patients [5]

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