2例多发性硬化患者输注奥雷利珠单抗后的血清疾病/血清疾病样反应。

Q1 Nursing
International journal of MS care Pub Date : 2023-09-01 Epub Date: 2023-09-14 DOI:10.7224/1537-2073.2022-080
Nicole Bou Rjeily, Bardia Nourbakhsh, Ellen M Mowry
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引用次数: 1

摘要

血清病(SS)是一种罕见的超敏反应,单克隆抗体可能会发生,ocrelizumab仅报告了1例SS病例。我们描述了2名多发性硬化症(MS)患者,他们在奥瑞珠单抗输注后出现SS/SS样反应(SSLRs)。一名45岁的男性和一名59岁的女性均患有原发性进行性多发性硬化症,在输注ocrelizumab后出现全身无力和关节痛。脑和脊髓核磁共振成像均未发现新的或增强性脱髓鞘病变。他们都有升高的炎症标志物和阴性的感染检查。随后,他们接受了类固醇减量治疗(第二例使用强效抗炎药),症状在几天后显著改善。这些病例表明,如果患者在接受ocrelizumab输注后出现新发关节痛,并且对类固醇反应迅速,则应怀疑SS/SSLR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum Sickness/Serum Sickness-like Reactions Following Ocrelizumab Infusion in 2 Patients With Multiple Sclerosis.

Serum sickness (SS) is a rare hypersensitivity reaction that can occur with monoclonal antibodies, and only 1 case of SS has been reported with ocrelizumab. We describe 2 patients with multiple sclerosis (MS) who developed SS/SS-like reactions (SSLRs) following ocrelizumab infusions. A man, aged 45 years, and a woman, aged 59 years, both with primary progressive MS, developed generalized weakness and arthralgias following their ocrelizumab infusions. Brain and spinal cord MRIs revealed no new or enhancing demyelinating lesions in both cases. They both had elevated inflammatory markers and negative infectious workups. They were subsequently treated for presumed SS with a steroid taper (and with potent anti-inflammatories in the second case), and symptoms improved dramatically after a few days. These cases suggest that SS/SSLRs should be suspected in a patient with new-onset arthralgia following ocrelizumab infusion who has an otherwise negative workup and rapid response to steroids.

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来源期刊
International journal of MS care
International journal of MS care Nursing-Advanced and Specialized Nursing
CiteScore
3.00
自引率
0.00%
发文量
40
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