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托珠单抗治疗糖皮质激素抵抗性巨细胞动脉炎伴进展性前部缺血性视神经病变。

Tocilizumab for giant cell arteritis with corticosteroid-resistant progressive anterior ischemic optic neuropathy.

机构信息

Service of Immunology and Allergy, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Lausanne, Switzerland; Transplantation Center, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Lausanne, Switzerland.

Service of Immunology and Allergy, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Lausanne, Switzerland.

出版信息

Joint Bone Spine. 2017 Oct;84(5):615-619. doi: 10.1016/j.jbspin.2017.04.009. Epub 2017 May 9.

Abstract

BACKGROUND

Giant cell arteritis is an inflammatory disorder of the medium- and large-size arteries. Permanent visual loss related to arteritic anterior ischemic optic neuropathy is among the most serious complications of this disease and initial treatment usually consists of high dose corticosteroids. There is no consensus in the literature concerning the optimal therapeutic approach in giant cell arteritis patients with corticosteroid-resistant arteritic anterior ischemic optic neuropathy.

CASE REPORT

A 73-year-old Caucasian female with biopsy-proven giant cell arteritis developed an acute visual loss of the right eye due to arteritic anterior ischemic optic neuropathy. Despite 5 daily methylprednisolone pulses, systemic symptoms persisted and rapid involvement of the controlateral eye was documented. Therefore, tocilizumab (humanised monoclonal antibody binding the human interleukin-6 receptor) was introduced as a potential salvage therapy with a swift consecutive resolution of the systemic symptoms and stabilization of the ophthalmic lesions.

CONCLUSIONS

Although a late effect of steroids pulses cannot be formally ruled out in this dramatic situation, tocilizumab likely offered a decisive effect in preventing bilateral blindness and may have contributed to steroid tapering. Tocilizumab may represent a new early effective second-line treatment option in corticosteroid-resistant anterior ischemic optic neuropathy. More data are needed to confirm this observation and to evaluate the safety profile of this treatment.

摘要

背景

巨细胞动脉炎是一种中、大动脉的炎症性疾病。与动脉炎性前部缺血性视神经病变相关的永久性视力丧失是该疾病最严重的并发症之一,初始治疗通常包括大剂量皮质类固醇。对于皮质类固醇耐药性动脉炎性前部缺血性视神经病变的巨细胞动脉炎患者,文献中尚无关于最佳治疗方法的共识。

病例报告

一位 73 岁的白人女性,经活检证实患有巨细胞动脉炎,因动脉炎性前部缺血性视神经病变而导致右眼急性视力丧失。尽管接受了 5 天的甲基强的松龙脉冲治疗,但全身症状仍持续存在,并记录到对侧眼睛迅速受累。因此,托珠单抗(一种与人白细胞介素-6 受体结合的人源化单克隆抗体)被引入作为一种潜在的挽救疗法,全身症状迅速缓解,眼部病变稳定。

结论

尽管在这种戏剧性的情况下不能正式排除类固醇脉冲的迟发效应,但托珠单抗可能在预防双眼失明方面发挥了决定性作用,并可能有助于皮质类固醇的减量。托珠单抗可能是皮质类固醇耐药性前部缺血性视神经病变的一种新的早期有效二线治疗选择。需要更多的数据来证实这一观察结果,并评估这种治疗的安全性。

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