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利妥昔单抗作为预防原发性局灶节段性肾小球硬化复发的抢先治疗:一种新方法。

Rituximab as a Preemptive Treatment to Prevent Recurrence of Primary Focal Segmental Glomerulosclerosis: A Novel Approach.

作者信息

El Khashab Sahier, El Khashab Omar, El Ghoneimy Mohamed, AbdelRassoul Mohamed Abdo

机构信息

From the Department of Internal Medicine and Nephrology, Cairo University, Cairo, Egypt.

出版信息

Exp Clin Transplant. 2019 Jun;17(3):326-329. doi: 10.6002/ect.2018.0027. Epub 2019 Mar 14.

DOI:10.6002/ect.2018.0027
PMID:30880653
Abstract

OBJECTIVES

Primary idiopathic focal segmental glomerulo-sclerosis is a serious disease, frequently progressing to end-stage kidney failure. Management of recurrence after kidney transplant is challenging despite multiple proposed therapeutic approaches. Available treatment for focal segmental glomeru-losclerosis recurrence is plasma exchange, intravenous cyclosporine, and rituximab. In this study, we investigated kidney transplant recipients with focal segmental glomerulosclerosis who were at high risk for recurrence. Patients were given preemptive rituximab at day 0 posttransplant.

MATERIALS AND METHODS

Between January 2013 and June 2017, our center had 8 patients with primary focal segmental glomerulosclerosis at high risk for recurrence who were scheduled for kidney transplant. These patients received a single rituximab infusion of 375 mg/m2 on day 0 posttransplant. Recurrence of focal segmental glomerulosclerosis posttransplant was defined as repeated proteinuria > 2 g/day, without evidence of clinical or biopsy-proven rejection.

RESULTS

Follow-up showed that none of our patients had immediate posttransplant proteinuria. Only 1 patient developed proteinuria at almost 4 months posttransplant. Mean follow-up duration was 8 months. With regard to complications, 2 patients had serious bacterial infections and 1 patient had cytomegalovirus infection.

CONCLUSIONS

Rituximab at day 0 posttransplant may be used safely to prevent focal segmental glomeru-losclerosis recurrence in the graft in the early posttransplant period. However, longer follow-up studies with larger series are needed.

摘要

目的

原发性特发性局灶节段性肾小球硬化是一种严重疾病,常进展为终末期肾衰竭。尽管有多种提出的治疗方法,但肾移植后复发的管理仍具有挑战性。局灶节段性肾小球硬化复发的可用治疗方法是血浆置换、静脉注射环孢素和利妥昔单抗。在本研究中,我们调查了有高复发风险的局灶节段性肾小球硬化肾移植受者。患者在移植后第0天接受抢先使用的利妥昔单抗治疗。

材料与方法

2013年1月至2017年6月期间,我们中心有8例有高复发风险的原发性局灶节段性肾小球硬化患者计划接受肾移植。这些患者在移植后第0天接受一次375mg/m²的利妥昔单抗输注。移植后局灶节段性肾小球硬化的复发定义为反复蛋白尿>2g/天,且无临床或活检证实的排斥反应证据。

结果

随访显示,我们的患者在移植后均无即刻蛋白尿。只有1例患者在移植后近4个月出现蛋白尿。平均随访时间为8个月。关于并发症,2例患者发生严重细菌感染,1例患者发生巨细胞病毒感染。

结论

移植后第0天使用利妥昔单抗可安全用于预防移植后早期移植物中局灶节段性肾小球硬化的复发。然而,需要更大样本量的更长时间的随访研究。

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