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抗 B 细胞治疗对难治性血小板减少症的系统性红斑狼疮和重叠综合征患者:长期随访和文献复习。

Anti B-cell therapy against refractory thrombocytopenia in SLE and MCTD patients: long-term follow-up and review of the literature.

机构信息

Department of Rheumatology, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

Lupus. 2013 Jun;22(7):664-74. doi: 10.1177/0961203313485489. Epub 2013 Apr 23.

Abstract

OBJECTIVE

The objective of this study was to retrospectively evaluate the clinical and immunological effects of anti-B cell treatment in patients with systemic lupus erythematosus (SLE) and mixed connective-tissue disease (MCTD) with autoimmune thrombocytopenia (AITP) refractory to conventional immunosuppressive treatment.

METHODS

Rituximab (RTX) was added to the ongoing treatment of 16 patients (median age 36 years, range 17-84, all female) with treatment-resistant AITP. Thirteen patients had SLE and three had MCTD. RTX was given intravenously on four occasions during four consecutive weeks at a dose of 375 mg/m(2). Clinical and laboratory disease activity variables recorded at every follow-up visit were analyzed.

RESULTS

The median disease duration before RTX treatment was nine years (range 0.2-27) and the median post-treatment follow-up time was 28 months (range 3 to 92). Ten patients (63%) were treated repeatedly with RTX during the follow-up period. Complete depletion of B cells was achieved in 94% of cases one month after RTX treatment. A significant increase (p = 0.0001) of platelet counts was seen already after one month (median 58 × 10(9)/ml vs 110 × 10(9)/ml) whereas within three months platelet counts normalized in 10 patients (median 223 × 10(9)/ml). Three patients did not respond to RTX treatment (median platelet count 69 × 10(9)/ml). High titers of anti-platelet antibodies were detected in seven patients before RTX treatment, and the autoantibody titers decreased significantly (p < 0.03) after RTX treatment in six of these patients who also achieved complete remission. A review of the literature revealed 24 articles including 18 case reports, one retrospective cohort study and five prospective studies documenting the outcomes of 65 RTX-treated patients with SLE- or MCTD-related thrombocytopenia with an overall treatment response rate of 80%. In conclusion, these findings indicate that RTX is an additional potent therapeutic treatment option for SLE patients with AITP refractory to conventional immunosuppressive treatment whereas best response may be expected in patients with high titers of anti-platelet antibodies at baseline.

摘要

目的

本研究旨在回顾性评估抗 B 细胞治疗对常规免疫抑制治疗无效的系统性红斑狼疮(SLE)和混合性结缔组织病(MCTD)合并自身免疫性血小板减少症(AITP)患者的临床和免疫学影响。

方法

在 16 例(中位年龄 36 岁,范围 17-84 岁,均为女性)常规免疫抑制治疗无效的 AITP 患者中,加用利妥昔单抗(RTX)治疗。13 例患者为 SLE,3 例为 MCTD。RTX 在 4 周内连续 4 次静脉滴注,剂量为 375mg/m2。分析每次随访时记录的临床和实验室疾病活动变量。

结果

RTX 治疗前的中位疾病病程为 9 年(范围 0.2-27 年),治疗后中位随访时间为 28 个月(范围 3-92 个月)。10 例(63%)患者在随访期间重复使用 RTX 治疗。RTX 治疗后 1 个月,94%的患者 B 细胞完全耗竭。1 个月时血小板计数显著升高(p=0.0001)(中位数 58×109/ml 与 110×109/ml),3 个月内 10 例患者血小板计数恢复正常(中位数 223×109/ml)。3 例患者对 RTX 治疗无反应(中位数血小板计数 69×109/ml)。7 例患者在 RTX 治疗前检测到高滴度抗血小板抗体,其中 6 例患者在 RTX 治疗后抗体滴度显著降低(p<0.03),并获得完全缓解。文献复习发现 24 篇文章,包括 18 例病例报告、1 项回顾性队列研究和 5 项前瞻性研究,共纳入 65 例接受 RTX 治疗的 SLE 或 MCTD 相关血小板减少症患者,总体治疗反应率为 80%。结论:这些发现表明,RTX 是一种额外的有效治疗选择,可用于常规免疫抑制治疗无效的 SLE 合并 AITP 患者,而基线时高滴度抗血小板抗体的患者可能有更好的反应。

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