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复发性特发性膜性肾病:通过方案活检进行早期诊断和抗 CD20 单克隆抗体治疗。

Recurrent idiopathic membranous nephropathy: early diagnosis by protocol biopsies and treatment with anti-CD20 monoclonal antibodies.

机构信息

Department of Internal Medicine, Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

出版信息

Am J Transplant. 2009 Dec;9(12):2800-7. doi: 10.1111/j.1600-6143.2009.02851.x. Epub 2009 Oct 21.

DOI:10.1111/j.1600-6143.2009.02851.x
PMID:19845581
Abstract

Membranous nephropathy (MN) recurs posttransplant in 42% of patients. We compared MN recurrence rates in a historical cohort transplanted between 1990 and 1999 and in a current cohort diagnosed by protocol biopsies, we analyzed the progression of the disease and we assessed the effects of anti-CD20 antibodies (Rituximab) on recurrent MN. The incidence of recurrent MN was similar in the historical (53%) and the current cohorts (41%), although in the later the diagnosis was made earlier (median, 4[2-21] months vs. 83[6-149], p = 0.002) and the disease was clinically milder. Twelve out of 14 patients (86%) with recurrent MN in the current cohort had progressive increases in proteinuria. Eight recipients were treated with Rituximab after their proteinuria increased from median, 211 mg/day (64-4898) at diagnosis to 4489 (898-13 855) (p = 0.038). Twelve months post-Rituximab, 75% of patients had either partial (PR) or complete remission (CR). After 24 months 6/7 (86%) had PR/CR and one patient relapsed. Posttreatment biopsies showed resorption of electron dense immune deposits in 6/7 cases and were negative for C3 (4/7) and IgG (3/7). Protocol biopsies allow early diagnosis of subclinical recurrent MN, which is often progressive. Treatment of recurrent MN with Rituximab is promising and should be evaluated in a prospective randomized controlled trial.

摘要

膜性肾病 (MN) 在 42%的移植后患者中复发。我们比较了 1990 年至 1999 年期间移植的历史队列和通过协议活检诊断的当前队列中的 MN 复发率,分析了疾病的进展,并评估了抗 CD20 抗体(利妥昔单抗)对复发性 MN 的影响。历史队列(53%)和当前队列(41%)的复发性 MN 发生率相似,尽管后者的诊断更早(中位数,4[2-21]个月与 83[6-149],p=0.002),且疾病的临床表现更轻微。在当前队列中,14 例复发性 MN 中有 12 例(86%)的蛋白尿持续增加。8 例患者在蛋白尿从诊断时的中位数 211 mg/天(64-4898)增加至 4489(898-13855)时(p=0.038)接受了利妥昔单抗治疗。利妥昔单抗治疗后 12 个月,75%的患者有部分缓解(PR)或完全缓解(CR)。24 个月后,6/7(86%)例有 PR/CR,1 例复发。治疗后活检显示 6/7 例电子致密免疫沉积物吸收,4/7 例 C3 阴性(4/7)和 IgG 阴性(3/7)。协议活检可早期诊断亚临床复发性 MN,其通常是进行性的。用利妥昔单抗治疗复发性 MN 有希望,应在前瞻性随机对照试验中进行评估。

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