Sellam Jérémie, Rouanet Stéphanie, Hendel-Chavez Houria, Miceli-Richard Corinne, Combe Bernard, Sibilia Jean, Le Loët Xavier, Tebib Jacques, Jourdan Rosemary, Dougados Maxime, Taoufik Yassine, Mariette Xavier
Hôpital Saint-Antoine, AP-HP, and Université Pierre et Marie Curie Paris 06, Paris, France.
Arthritis Rheum. 2013 Sep;65(9):2253-61. doi: 10.1002/art.38023.
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.
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).
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.
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.
类风湿关节炎(RA)患者外周血B细胞向滑膜的迁移可能预测其对利妥昔单抗(RTX)的临床反应。我们开展本研究以调查参与B细胞迁移的趋化因子血清水平是否与B细胞耗竭前记忆B细胞的血液水平或B细胞活化生物标志物的血清水平相关,以及趋化因子水平是否可预测RTX反应性。
采用流式细胞术(CD27、IgD)分析208例RA患者和70例对照者的血液B细胞亚群,并检测血清B细胞活化生物标志物(类风湿因子、抗环瓜氨酸肽、游离轻链、IgG、IgA、IgM和BAFF)。采用酶联免疫吸附测定法测定患者和对照者血清CCL19、CXCL12和CXCL13趋化因子水平。对RA患者给予首个疗程的RTX,并根据欧洲抗风湿病联盟(EULAR)标准在第24周评估反应。结果以比值比(OR)和95%置信区间(95%CI)表示。
与对照组相比,RA患者所有趋化因子水平均升高,且这些水平与CD27+记忆B细胞频率呈负相关。CCL19和CXCL13水平分别与6种血清B细胞生物标志物水平和4种血清B细胞生物标志物水平相关。单因素分析显示,CCL19水平与EULAR反应呈正相关(OR 1.43 [95%CI 1.08 - 1.90],P = 0.01)。多因素分析显示,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,这种相关性不再存在。
CXCL13和CCL19反映血液B细胞紊乱,其水平与其他血清B细胞生物标志物水平相关。因此,CXCL13和CCL19是RA患者血清B细胞生物标志物的替代指标。血清CCL19检测是B细胞介导的RA亚型的一个新标志,可能预测对RTX的临床反应。