Autoantigen Peptide‐8‐Arm Polyethylene Glycol‐Dyes Specifically Recognize Antigen‐Specific B Cells and Improve the Diagnosis of Rheumatoid Arthritis

医学 类风湿性关节炎 免疫学 免疫系统 自身免疫性疾病 疾病 自身抗体 关节炎 自身免疫 B细胞 癌症研究 鉴定(生物学) 抗体 结缔组织病 免疫病理学
作者
S Liu,Changrong Shi,Lulu Cao,Jing Huang,Yang Xie,Chaonan Wei,Yuejiao Xiong,Bin Shen,Xuanlin Cai,Teng Li,Danxue Zhu,Ranran Yao,Wenhao Lin,Jin Xu,Ping Wang,Xiangyu Fang,Yingni Li,Huaqun Zhu,Yan Ding,Qian Guo
出处
期刊:Arthritis & rheumatology [Wiley]
标识
DOI:10.1002/art.70003
摘要

OBJECTIVES: Rheumatoid arthritis (RA) is a systemic chronic disabling autoimmune disease with high autoantibody production. However, approximately one-third of patients with RA are autoantibodies-negative lacking biomarkers. Antigen-specific B cells are critical participants in RA pathogenesis by producing autoantibodies and driving inflammation and joint damage. Nevertheless, the limited detection methods have impeded in-depth studies on these cells. This study aimed to develop a novel probe to precisely recognize these cells and evaluate their diagnostic potential for RA. METHODS: Autoantigen peptide-8-arm polyethylene glycol (PEG; APP) - dyes, named APP-dyes, were constructed by conjugating classical autoantigens with a multifunctional polymer material, eight-arm PEG-maleimide. The specificity and efficiency of APP-dyes in detecting antigen-specific B cells were analyzed by flow cytometry. The pathogenicity of antigen-specific B cells isolated by APP-dyes was assessed through in vitro culture and adoptive transfer assays. The diagnostic value of APP-dyes in distinguishing RA was also systemically examined. RESULTS: The APP-dyes could efficiently and specifically recognize antigen-specific B cells in patients with RA, experimental arthritis mice, and spontaneous arthritis mice. Antigen-specific B cells isolated by APP-dyes were highly active in autoantibody secretion and arthritis initiation. The sensitivity and/or specificity of mutated citrullinated vimentin-specific B cells and citrullinated Type II collagen-specific B cells identified by the APP-dyes were 73.33% and/or 92.5% and 60.00% and/or 91.25% for RA diagnosis, respectively. Notably, these cells also showed substantial diagnostic performance in anti-cyclic citrullinated peptide-negative and early patients with RA. Moreover, combining antigen-specific B cells with their corresponding autoantibodies further increased the diagnostic accuracy. CONCLUSIONS: These findings indicated APP-dyes as an effective and clinically applicable tool for investigating the mechanisms underlying antigen-specific B cells and distinguishing RA.
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