Immune reconstitution, glomerulonephritis, and successful treatment with rituximab.

Clinical Nephrology. Case Studies Pub Date : 2020-09-01 eCollection Date: 2020-01-01 DOI:10.5414/CNCS110061
George Vasquez-Rios, John C Edwards, Saketh Tummala, Ashley Chapel, Ramez Sunna, David S Brink, Christopher Laohathai, Thanh-Mai Vo
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Abstract

Background: Alemtuzumab can induce secondary autoimmunity affecting multiple organs. While kidney involvement is uncommon, it can be associated with devastating forms of glomerulonephritis (GN).

Case presentation: A 32-year-old African American woman presented with hypertension, proteinuria, and progressive renal failure. Her medical history was remarkable for secondary progressive multiple sclerosis (SPMS). She had received her first induction dose of alemtuzumab 1 year prior to presentation. Upon evaluation, she had scanning speech, multidirectional nystagmus, and mild edema. Her serum creatinine was 2 mg/dL. Urine studies revealed proteinuria and microscopic hematuria. Her serologic tests were positive for c-antineutrophil cytoplasmic antibodies (> 1 : 640). In addition, she was found to have new-onset severe thyroid dysfunction with antibodies against thyroglobulin and thyroid peroxidase. Kidney biopsy was diagnostic for pauci-immune crescentic GN. The patient was treated with methylprednisolone and rituximab with subsequent renal, thyroid, and neurological recovery.

Conclusion: This is an atypical case of GN following therapy with alemtuzumab. We hypothesize that immune reconstitution may be a potential mechanism. Alemtuzumab is a new treatment for SPMS that can be associated with GN. Practice guidelines should address the management of its renal complications.

Abstract Image

Abstract Image

免疫重建,肾小球肾炎,利妥昔单抗治疗成功。
背景:阿仑单抗可诱导累及多器官的继发性自身免疫。虽然肾脏受累并不常见,但它可能与破坏性形式的肾小球肾炎(GN)有关。病例介绍:一名32岁的非裔美国女性,表现为高血压、蛋白尿和进行性肾衰竭。她的病史是继发性进行性多发性硬化症(SPMS)。她在就诊前1年接受了第一次阿仑单抗诱导剂量。经评估,她有扫描性言语,多向眼球震颤和轻度水肿。她的血清肌酐为2 mg/dL。尿液检查显示蛋白尿和显微镜下血尿。她的血清学试验c-抗中性粒细胞细胞质抗体阳性(> 1:40 0)。此外,她被发现有新发的严重甲状腺功能障碍,抗甲状腺球蛋白和甲状腺过氧化物酶抗体。肾活检诊断为缺乏免疫的月牙形GN。患者接受甲基强的松龙和利妥昔单抗治疗,随后肾脏、甲状腺和神经系统恢复。结论:这是一例阿仑单抗治疗后的非典型GN病例。我们假设免疫重建可能是一种潜在的机制。阿仑妥珠单抗是一种可与GN相关的SPMS新疗法。实践指南应解决其肾脏并发症的管理。
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