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高灵敏度B细胞分析可预测类风湿关节炎患者对利妥昔单抗治疗的反应。

Highly sensitive B cell analysis predicts response to rituximab therapy in rheumatoid arthritis.

作者信息

Dass Shouvik, Rawstron Andy C, Vital Edward M, Henshaw Karen, McGonagle Dennis, Emery Paul

机构信息

University of Leeds, and Leeds Teaching Hospitals National Health Service Trust, Leeds, UK.

出版信息

Arthritis Rheum. 2008 Oct;58(10):2993-9. doi: 10.1002/art.23902.

Abstract

OBJECTIVE

In rheumatoid arthritis (RA), B cell depletion occurs in all patients treated with rituximab, but the clinical responses to rituximab are variable. A highly sensitive assay was used to test the hypothesis that B cell depletion is variable, and that incomplete depletion leads to a poorer outcome.

METHODS

Sixty patients with active RA unresponsive to anti-tumor necrosis factor agents received two 1-gram infusions of rituximab. B cell numbers were measured by highly sensitive flow cytometry before and after each infusion and at 3-month intervals thereafter. A reduction in B cell levels below 0.0001x10(9)/liter was defined as complete depletion (compared with 0.05x10(9)/liter by conventional cytometry). Clinical responses were measured using the European League Against Rheumatism (EULAR) criteria.

RESULTS

At 6 months, 92% of patients had a moderate-to-good clinical response according to the EULAR criteria. B cells were detected in 63% of patients after the first infusion of rituximab (median level 0.0009x10(9)/liter [range<0.0001-0.0015x10(9)/liter), and these patients had poorer clinical outcomes than patients with complete depletion. At 9 months, 82% of patients with complete depletion had a moderate-to- good EULAR response, compared with 43% of those with partial depletion (P=0.01). At 12 months, 59% of complete responders had a moderate-to-good EULAR response, compared with 21% of those with partial depletion (P=0.01). Patients in whom B cells were depleted only after the second infusion did no better than those in whom depletion was never complete and had poorer clinical outcomes than those in whom depletion was initially complete.

CONCLUSION

This study is the first to show, using a highly sensitive analysis, that rituximab therapy is associated with variable diminution in B cell numbers. A lack of complete depletion of B cells after 1 infusion was associated with a poorer outcome.

摘要

目的

在类风湿关节炎(RA)中,所有接受利妥昔单抗治疗的患者都会出现B细胞耗竭,但对利妥昔单抗的临床反应存在差异。本研究采用一种高灵敏度检测方法来验证以下假设:B细胞耗竭存在差异,且不完全耗竭会导致较差的治疗结果。

方法

60例对抗肿瘤坏死因子药物无反应的活动性RA患者接受了两次1克剂量的利妥昔单抗静脉输注。在每次输注前后以及之后每隔3个月,通过高灵敏度流式细胞术检测B细胞数量。将B细胞水平降至0.0001×10⁹/升以下定义为完全耗竭(传统流式细胞术检测的阈值为0.05×10⁹/升)。使用欧洲抗风湿病联盟(EULAR)标准评估临床反应。

结果

6个月时,根据EULAR标准,92%的患者有中度至良好的临床反应。首次输注利妥昔单抗后,63%的患者检测到B细胞(中位水平为=0.0009×10⁹/升[范围<0.0001 - 0.0015×10⁹/升]),这些患者的临床结局比完全耗竭的患者更差。9个月时,完全耗竭的患者中有82%有中度至良好的EULAR反应,而部分耗竭的患者中这一比例为43%(P = 0.01)。12个月时,完全反应者中有59%有中度至良好的EULAR反应,而部分耗竭的患者中这一比例为21%(P = 0.01)。仅在第二次输注后才出现B细胞耗竭的患者,其治疗效果并不优于从未完全耗竭的患者,且临床结局比最初就完全耗竭的患者更差。

结论

本研究首次使用高灵敏度分析表明,利妥昔单抗治疗导致的B细胞数量减少存在差异。首次输注后B细胞未完全耗竭与较差的治疗结果相关。

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