首页> 外文期刊>Arthritis and Rheumatism >CCL19, a B cell chemokine, is related to the decrease of blood memory B cells and predicts the clinical response to rituximab in patients with rheumatoid arthritis
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CCL19, a B cell chemokine, is related to the decrease of blood memory B cells and predicts the clinical response to rituximab in patients with rheumatoid arthritis

机译:B细胞趋化因子CCL19与血液记忆B细胞减少有关,并预测类风湿关节炎患者对利妥昔单抗的临床反应

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Objective Migration of B cells from peripheral blood to the synovium in patients with rheumatoid arthritis (RA) may predict clinical response to rituximab (RTX). We undertook this study to investigate whether serum levels of chemokines involved in B cell trafficking are correlated with blood levels of memory B cells or serum levels of B cell activation biomarkers before B cell depletion and whether chemokine levels predict RTX responsiveness. Methods Blood B cell subsets were analyzed by flow cytometry (CD27, IgD), and serum B cell activation biomarkers (rheumatoid factor, anti-cyclic citrullinated peptide, free light chains, IgG, IgA, IgM, and BAFF) were measured in 208 RA patients and 70 control subjects. Serum CCL19, CXCL12, and CXCL13 chemokine levels in patients and controls were determined by enzyme-linked immunosorbent assay. The first course of RTX was administered to RA patients, and the response was evaluated at week 24 according to European League Against Rheumatism (EULAR) criteria. Results were expressed as the odds ratio (OR) and 95% confidence interval (95% CI). Results Levels of all chemokines were increased in RA patients compared with controls, and levels were inversely correlated with CD27+ memory B cell frequency. CCL19 and CXCL13 levels correlated with levels of 6 serum B cell biomarkers and 4 serum B cell biomarkers, respectively. By univariate analysis, the CCL19 level was positively associated with EULAR response (OR 1.43 [95% CI 1.08-1.90], P = 0.01). By multivariate analysis, the CCL19 level was predictive of a response to RTX (OR 1.48 [95% CI 1.06-2.06], P = 0.02), but this did not persist after adjustment for autoantibody status. Conclusion CXCL13 and CCL19 reflect blood B cell disturbances and their levels correlate with those of other serum B cell biomarkers. CXCL13 and CCL19 are, therefore, surrogate measures for serum B cell biomarkers in RA. Serum CCL19 measurement is a new hallmark of the B cell-mediated RA subtype and may predict clinical response to RTX.
机译:目的类风湿关节炎(RA)患者的B细胞从外周血向滑膜的迁移可预测对利妥昔单抗(RTX)的临床反应。我们进行了这项研究,以调查参与B细胞运输的血清趋化因子水平是否与记忆B细胞的血液水平或B细胞耗竭之前血清B细胞活化生物标志物的水平相关,以及趋化因子水平是否预测RTX反应性。方法用流式细胞仪(CD27,IgD)分析血B细胞亚群,并在208 RA中测定血清B细胞活化生物标志物(类风湿因子,抗环瓜氨酸肽,自由轻链,IgG,IgA,IgM和BAFF)。患者和70名对照对象。通过酶联免疫吸附测定法测定患者和对照组的血清CCL19,CXCL12和CXCL13趋化因子水平。将RTX的第一个疗程施用于RA患者,并根据欧洲风湿病联盟(EULAR)标准在第24周评估反应。结果表示为优势比(OR)和95%置信区间(95%CI)。结果与对照相比,RA患者所有趋化因子水平均升高,且水平与CD27 +记忆B细胞频率呈负相关。 CCL19和CXCL13的水平分别与6种血清B细胞生物标志物和4种血清B细胞生物标志物的水平相关。通过单因素分析,CCL19水平与EULAR反应呈正相关(OR 1.43 [95%CI 1.08-1.90],P = 0.01)。通过多变量分析,CCL19水平可预测对RTX的反应(OR 1.48 [95%CI 1.06-2.06],P = 0.02),但在调整自身抗体状态后并没有持续。结论CXCL13和CCL19反映了血液B细胞紊乱,其水平与其他血清B细胞生物标志物相关。因此,CXCL13和CCL19是RA中血清B细胞生物标志物的替代指标。血清CCL19的测量是B细胞介导的RA亚型的新标志,可以预测对RTX的临床反应。

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