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

被引:10
作者
Liu, Suying [1 ,2 ]
Yang, Yanlei [1 ,2 ]
Zeng, Liuting [1 ,2 ]
Wang, Li [1 ,2 ]
He, Chengmei [1 ,2 ]
Chen, Zhilei [1 ,2 ]
Sun, Jinlei [1 ,2 ]
Lyu, Taibiao [1 ,2 ]
Wang, Mu [3 ]
Chen, Hua [1 ,2 ]
Zhang, Fengchun [1 ,2 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Rheumatol & Clin Immunol, 1 Shuai Fu Yuan, Beijing 100730, Peoples R China
[2] Minist Educ, Key Lab Rheumatol & Clin Immunol, Beijing, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Stomatol, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
SS; naive T; follicular helper T; TOX; interferon-alpha; JAK-STAT; SALIVARY-GLAND; IMMUNE-RESPONSE; B-CELLS; PATHOGENESIS; ASSOCIATION; ACTIVATION; ROLES;
D O I
10.1093/rheumatology/keac304
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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] .
引用
收藏
页码:946 / 957
页数:12
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