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利妥昔单抗治疗抗肾小球基底膜抗体病:基于病例的综述。

Anti-glomerular basement membrane antibody disease treated with rituximab: A case-based review.

机构信息

Department of Medicine, Division of Rheumatology, Case Western Reserve University/MetroHealth Medical Center, Cleveland, OH 44109, USA.

出版信息

Semin Arthritis Rheum. 2013 Jun;42(6):567-72. doi: 10.1016/j.semarthrit.2012.10.007. Epub 2013 Jan 24.

Abstract

OBJECTIVES

To report the successful use of rituximab in a patient with anti- glomerular basement membrane (GBM) antibody disease and to review the literature regarding rituximab use in anti-GBM mediated disease.

METHODS

We report a case of anti-GBM antibody disease with both anti-GBM antibodies and anti-myeloperoxidase (MPO) specific p-ANCA, who developed thrombotic thrombocytopenic purpura (TTP) on high dose prednisone, plasmapheresis, and cyclophosphamide therapy. The patient was then treated with rituximab. We analyzed the clinical features of five additional patients of anti-GBM disease treated with rituximab identified through a systematic literature review.

RESULTS

Our patient was 68-year-old female who presented with acute renal failure. Renal biopsy showed crescentic glomerulonephritis with linear deposits of IgG antibody along the glomerular basement membrane. Treatment was initiated with high dose prednisone, plasmapheresis and oral cyclophosphamide, with subsequent development of leukopenia and TTP and discontinuance of cyclophosphamide. Treatment with rituximab was initiated with clinical improvement of her hematological parameters but not her renal function. Among the five previously reported cases of anti-GBM disease treated with rituximab, three received brief course of IV cyclophosphamide prior to use of rituximab. Except one patient, all recovered renal function and remained dialysis independent. The anti-GBM antibody level remained undetected in all patients.

CONCLUSIONS

Combination of prednisone, plasmapheresis, and rituximab can be an effective therapy in patients with an anti-GBM antibody disease complicated with TTP.

摘要

目的

报道利妥昔单抗成功治疗抗肾小球基底膜(GBM)抗体病患者,并复习文献中关于利妥昔单抗治疗抗 GBM 介导疾病的应用。

方法

我们报告了一例抗 GBM 抗体病患者,其抗 GBM 抗体和抗髓过氧化物酶(MPO)特异性 p-ANCA 均为阳性,在大剂量泼尼松、血浆置换和环磷酰胺治疗后发生血栓性血小板减少性紫癜(TTP)。随后,该患者接受了利妥昔单抗治疗。我们通过系统文献复习分析了另外 5 例接受利妥昔单抗治疗的抗 GBM 疾病患者的临床特征。

结果

我们的患者为 68 岁女性,表现为急性肾衰竭。肾活检显示新月体性肾小球肾炎,免疫球蛋白 G 抗体沿肾小球基底膜呈线性沉积。治疗方案为大剂量泼尼松、血浆置换和口服环磷酰胺,随后出现白细胞减少和 TTP,停用环磷酰胺。开始利妥昔单抗治疗后,患者血液学参数改善,但肾功能未恢复。在之前报道的 5 例接受利妥昔单抗治疗的抗 GBM 疾病患者中,有 3 例在使用利妥昔单抗之前接受了短暂的 IV 环磷酰胺治疗。除 1 例患者外,所有患者的肾功能均恢复,且无需透析。所有患者的抗 GBM 抗体水平均未检出。

结论

泼尼松、血浆置换和利妥昔单抗联合治疗可有效治疗伴有 TTP 的抗 GBM 抗体病患者。

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