Vasquez-Rios George, Edwards John C, Tummala Saketh, Chapel Ashley, Sunna Ramez, Brink David S, Laohathai Christopher, Vo Thanh-Mai
Internal Medicine Department, Saint Louis University School of Medicine.
Nephrology Division, Department of Medicine, Saint Louis University.
Clin Nephrol Case Stud. 2020 Sep 1;8:67-71. doi: 10.5414/CNCS110061. eCollection 2020.
Alemtuzumab can induce secondary autoimmunity affecting multiple organs. While kidney involvement is uncommon, it can be associated with devastating forms of glomerulonephritis (GN).
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.
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.
阿仑单抗可诱发影响多个器官的继发性自身免疫。虽然肾脏受累并不常见,但可能与严重的肾小球肾炎(GN)形式相关。
一名32岁非裔美国女性出现高血压、蛋白尿和进行性肾衰竭。她有继发性进展性多发性硬化症(SPMS)病史。在就诊前1年,她接受了首次诱导剂量的阿仑单抗治疗。评估时,她存在扫描式言语、多向性眼球震颤和轻度水肿。她的血清肌酐为2mg/dL。尿液检查显示蛋白尿和镜下血尿。她的血清学检查抗中性粒细胞胞浆抗体呈阳性(>1:640)。此外,发现她出现新发的严重甲状腺功能障碍,伴有抗甲状腺球蛋白和甲状腺过氧化物酶抗体。肾脏活检诊断为寡免疫性新月体性GN。患者接受甲泼尼龙和利妥昔单抗治疗后,肾脏、甲状腺和神经功能得以恢复。
这是一例阿仑单抗治疗后发生GN的非典型病例。我们推测免疫重建可能是一种潜在机制。阿仑单抗是SPMS的一种新治疗方法,可能与GN相关。实践指南应涉及对其肾脏并发症的管理。