TOX promotes follicular helper T cell differentiation in patients with primary Sjogren's syndrome

Rheumatology (Oxford, England)(2023)

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摘要
Objectives. Whether naive CD4(+) T cells are dysregulated and associated with the overactivation of CD4(+) T cells in primary SS (pSS) remains unclear. We aimed to explore the role and underlying mechanism of naive CD4(+) T cells in pSS. Methods. We examined the activation, proliferation and differentiation of naive CD4(+) T cells from pSS patients and healthy controls. Differentially expressed genes were identified using RNA sequencing, and were overexpressed or silenced to determine the gene regulating follicular helper T (Tfh) cells. Assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) with chromatin immunoprecipitation with high-throughput sequencing (ChIP-seq) was performed to explore the epigenetic mechanism. Naive CD4(+) T cells were treated with pSS-related cytokines to explore the upstream signalling pathway. Results. pSS naive CD4(+) T cells had higher potentials of activation, proliferation and differentiation towards Tfh cells. Thymocyte selection-associated high mobility group box protein (TOX) was upregulated in pSS naive CD4(+) T cells and promoted T cell activation and Tfh cell polarization. TOX silencing in pSS naive CD4(+) T cells downregulated B cell lymphoma 6 (BCL6) expression and altered levels of multiple Tfh-associated genes. ChIP-seq analysis implied that TOX bound to the BCL6 locus, where there were accessible regions found by ATAC-seq. IFN-alpha induced TOX overexpression, which was attenuated by Janus kinase (JAK) and signal transducer and activator of transcription 1 (STAT1) inhibitors. Conclusion. Our data suggest that TOX in pSS naive CD4(+) T cells is upregulated, which facilitates Tfh cell differentiation. Mechanistically, IFN-alpha induces TOX overexpression in naive CD4(+) T cells through JAK-STAT1 signalling and TOX regulates BCL6 expression. Therefore, IFN-alpha-JAK-STAT1 signalling and TOX might be potential therapeutic targets in pSS. [GRAPHICS] .
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关键词
SS,naive T,follicular helper T,TOX,interferon-alpha,JAK-STAT
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