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阿达木单抗治疗期间发生的进展型多发性硬化拓宽了抗TNF-α治疗相关脱髓鞘疾病的范围。

PPMS onset upon adalimumab treatment extends the spectrum of anti-TNF-α therapy-associated demyelinating disorders.

作者信息

Engel Sinah, Luessi Felix, Mueller Aneka, Schopf Rudolf E, Zipp Frauke, Bittner Stefan

机构信息

Department of Neurology, Focus Program Translational Neuroscience (FTN), and Immunotherapy (FZI), Rhine-Main Neuroscience Network (rmn), University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

Department of Dermatology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

出版信息

Ther Adv Neurol Disord. 2020 Jan 2;13:1756286419895155. doi: 10.1177/1756286419895155. eCollection 2020.

Abstract

Since their introduction in 1999, anti-tumour necrosis factor-α (anti-TNF-α) therapies have been suspected repeatedly to be associated with the occurrence of central nervous system (CNS) demyelinating disorders, including multiple sclerosis (MS). However, recent publications were restricted to descriptions of monophasic demyelinating events or cases of relapsing-remitting MS (RRMS). We here provide the first case report of primary progressive MS (PPMS) onset upon anti-TNF-α therapy as well as a literature review of previously published cases of anti-TNF-α therapy-associated MS onset. The 51-year old male patient was treated with adalimumab due to psoriasis arthritis. About 18 months after treatment initiation, he developed slowly progressing neurological deficits including gait impairment, paraesthesia of the lower limbs, strangury and visual impairment, which led to the discontinuation of adalimumab therapy. Magnetic resonance imaging of the brain and the spinal cord revealed multiple inflammatory lesions and cerebrospinal fluid examination showed slight pleocytosis and positive oligoclonal bands. Thus, PPMS was diagnosed according to the 2017 revision of the McDonald criteria. As PPMS often causes only subtle symptoms in the beginning and early treatment discontinuation of anti-TNF-α therapy seems essential to improve the patient's outcome, we think that it is important to increase the awareness of slowly progressing neurological deficits as a potential adverse event of anti-TNF-α therapy among all clinicians involved in the initiation and monitoring of these drugs. In addition, the occurrence of both RRMS and progressive MS upon anti-TNF-α therapy might suggest a shared TNF-α-mediated pathophysiological mechanism in the evolution of all MS subtypes.

摘要

自1999年引入以来,抗肿瘤坏死因子-α(抗TNF-α)疗法多次被怀疑与中枢神经系统(CNS)脱髓鞘疾病的发生有关,包括多发性硬化症(MS)。然而,最近的出版物仅限于对单相脱髓鞘事件或复发缓解型MS(RRMS)病例的描述。我们在此提供首例抗TNF-α治疗后发生原发性进行性MS(PPMS)的病例报告,并对先前发表的抗TNF-α治疗相关MS发病病例进行文献综述。该51岁男性患者因银屑病关节炎接受阿达木单抗治疗。治疗开始约18个月后,他出现了缓慢进展的神经功能缺损,包括步态障碍、下肢感觉异常、尿痛和视力障碍,这导致阿达木单抗治疗中断。脑和脊髓的磁共振成像显示多个炎性病灶,脑脊液检查显示轻度细胞增多和寡克隆带阳性。因此,根据2017年修订的麦克唐纳标准诊断为PPMS。由于PPMS在开始时通常仅引起轻微症状,并且早期停用抗TNF-α治疗似乎对改善患者预后至关重要,我们认为提高所有参与这些药物起始和监测的临床医生对缓慢进展的神经功能缺损作为抗TNF-α治疗潜在不良事件的认识非常重要。此外,抗TNF-α治疗后RRMS和进行性MS的发生可能提示在所有MS亚型的演变中存在共同的TNF-α介导的病理生理机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28be/6940603/de86abd2224b/10.1177_1756286419895155-fig1.jpg

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