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Methods and kits for assessing clinical outcome of autoimmune disease

机译:评估自身免疫性疾病临床结局的方法和试剂盒

摘要

By comparing biomarkers of CD45RA, TNF-alpha, and/or CXCR5 from a CD3 + CD4 + T cell population, eg, where the subject ceases to take a biological disease modifying anti-rheumatic drug (DMARD) Methods and kits for assessing the clinical outcome of an autoimmune disease, specifically disease relapse, are disclosed. In a specific embodiment, the ratio of the first subset of CD3 + CD4 + CD45RA TNFA + (memory) T cells to the second subset comprising CD3 + CD4 + CD45RA + TNFA + (untreated) T cells is determined. However, an increase in this ratio is indicative of juvenile idiopathic arthritis (JIA) disease flare-up status. In another embodiment, enrichment of the CD45RA - CR5 + subset among T cell populations indicates a possible flare-up in JIA due to enhanced memory retention through B cell interactions. In another embodiment, additional markers including IL-6, CCR6, CD152, and PD1 are also determined. [Selection diagram] Fig. 3
机译:通过比较CD3 + CD4 + T细胞群体中CD45RA,TNF-α和/或CXCR5的生物标志物,例如,受试者停止采取生物疾病改良措施抗风湿药(DMARD)公开了用于评估自身免疫性疾病,特别是疾病复发的临床结果的方法和试剂盒。在一个具体的实施方案中,CD3 + CD4 + CD45RA - TNFA + 的第一子集的比例(内存)包含CD3 + CD4 + CD45RA + TNFA + 的第二个亚群的T细胞(未处理)是决心。但是,该比率的增加表示青少年特发性关节炎(JIA)疾病发作状态。在另一个实施方案中,T细胞群体中CD45RA - -CR5 + 子集的富集表明由于通过B细胞相互作用增强的记忆保持性,JIA中可能发生爆发。在另一个实施方案中,还确定了包括IL-6,CCR6,CD152和PD1的其他标记。 [选择图]图3

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