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Case Reports
. 2024 Jul 26:17:17562864241258787.
doi: 10.1177/17562864241258787. eCollection 2024.

A rare adverse effect in inebilizumab therapy for neuromyelitis optica spectrum disorder: a case report

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Case Reports

A rare adverse effect in inebilizumab therapy for neuromyelitis optica spectrum disorder: a case report

Xuefen Chen et al. Ther Adv Neurol Disord. .

Abstract

Inebilizumab is one of the monoclonal antibodies approved as maintenance therapy for aquaporin-4 immunoglobulin G-seropositive neuromyelitis optica spectrum disorder (NMOSD). It is a humanized monoclonal antibody targeting cluster of differentiation 19 (CD19). Common adverse reactions include urinary tract infections, nasopharyngitis, arthralgia, infusion reactions, headaches and a decrease in immunoglobulin levels. Here, we present a case of an NMOSD patient who experienced transient hyperCKaemia after the use of inebilizumab. The adverse reactions of this very rare monoclonal antibody drug improved after discontinuation.

Keywords: adverse effect; case report; hyperCKaemia; inebilizumab; neuromyelitis optica spectrum disorder.

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Figures

Figure 1.
Figure 1.
Spinal cord MRI taken at the first attack. Sagittal (a) and axial (b) MR images of the thoracic spine show a long-segment T2 hyperintensity. MRI, magnetic resonance imaging.
Figure 2.
Figure 2.
Spinal cord MRI taken during the inflammatory myelitis episode. Sagittal (a–c) and axial (d–f) MR images of the thoracic spine show a long-segment T2 hyperintensity, with increased enhancement observed. MRI, magnetic resonance imaging.
Figure 3.
Figure 3.
Timeline of the patient’s condition with relevant data of past episodes. (a) Relapse and treatment. (b) CK values. The red arrow indicates the time points of inebilizumab usage. AM, acute myelitis; CK, creatinine kinase; MMF, mycophenolate mofetil; ON, optic neuritis; RTX, rituximab.

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