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Multiplex serum cytokine monitoring as a prognostic tool in rheumatoid arthritis

机译:多重血清细胞因子监测作为类风湿关节炎的预后工具

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OBJECTIVES:Early optimized therapy of rheumatoid arthritis (RA) results in improved outcomes. The initiation of optimized therapy is hindered by the difficulty of early diagnosis and the limitations of current disease activity and therapeutic response assessment tools. Identifying patients requiring early combination DMARD/biologic therapy is currently a significant clinical challenge given the lack of definitive prognostic criteria. Since cytokines are soluble intracellular signaling molecules that modulate disease pathology in RA, we tested the recent conjecture that en mass serum cyto-kine measurement and monitoring will provide a useful tool for effective therapeutic management in RA. METHODS:We assayed the levels of 16 serum cytokines in 18 RA patients treated prospectively with methotrexate and from 18 unaffected controls. Specific mechanistic aspects of inflammatory pathology in the periphery could be discerned on a patient-specific basis from patients` serum cytokine profiles, information that may aid in the design of anti-cytokine biologic therapy. A serum Cytokine Activity Index (CAI) was also created using multi-variant analysis methods. RESULTS:Distinct cytokines were significantly elevated in RA patients relative to controls, and three distinct clusters with correlations to disease activity were identified. The Cytokine Activity Index correlated well with the therapeutic res-ponse; responders and non-responders in this cohort were distinguishable as early as one month post initiation of methotrexate therapy, well before clinical assessments of response are commonly completed. CONCLUSIONS:Clinical assessment tools could be derived from this approach that may provide a means to continually track patients, allowing intervention strategies to be better evaluated on a patient-specific basis and to identify residual cytokine activity that could be used to guide combination therapy.
机译:目的:对风湿性关节炎(RA)进行早期优化治疗可改善治疗效果。早期诊断的困难以及当前疾病活动和治疗反应评估工具的局限性阻碍了优化治疗的开始。由于缺乏明确的预后标准,因此识别需要早期DMARD /生物疗法联合治疗的患者目前是一项重大的临床挑战。由于细胞因子是可调节RA中疾病病理的可溶性细胞内信号分子,因此我们测试了最近的推测,即大量血清细胞因子的测量和监测将为RA中有效的治疗管理提供有用的工具。方法:我们分析了18例接受甲氨蝶呤治疗的RA患者和18例未患病对照的16种血清细胞因子的水平。可以根据患者的血清细胞因子谱来识别患者外周炎症病理的特定机制,这些信息可能有助于抗细胞因子生物疗法的设计。还使用多变量分析方法创建了血清细胞因子活性指数(CAI)。结果:相对于对照组,RA患者的独特细胞因子显着升高,并且鉴定出三个与疾病活动相关的不同簇。细胞因子活性指数与治疗反应密切相关。该人群的应答者和非应答者最早在甲氨蝶呤治疗开始后一个月就可以区分,远远早于对应答的临床评估。结论:可以从这种方法中获得临床评估工具,该工具可以提供一种持续追踪患者的方法,从而可以根据患者的具体情况更好地评估干预策略,并确定可用于指导联合治疗的残余细胞因子活性。

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