Watanabe Mitsuru, Masaki Katsuhisa, Tanaka Eizo, Matsushita Takuya, Isobe Noriko
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Fukuoka, JPN.
Department of Neurology, Kochi Medical School, Kochi University, Nankoku, JPN.
Cureus. 2024 Nov 7;16(11):e73205. doi: 10.7759/cureus.73205. eCollection 2024 Nov.
Eculizumab, a monoclonal antibody against complement C5, has been approved to prevent neuromyelitis optica spectrum disorder (NMOSD) relapse. Although complement activation leads to neuroinflammation and tissue necrosis in NMOSD attacks, clinical reports on the efficacy of eculizumab in the acute phase of NMOSD are limited. To clarify its effectiveness against clinical symptoms in NMOSD attacks, we described five patients with NMOSD who were administered eculizumab soon after treatment for an attack. The patients included four female patients and one male patient aged 50-93 years. The index attacks were optic neuritis in three cases, myelitis in one case, and brainstem encephalitis and myelitis in one case. Three patients had not received any maintenance therapy. Although all patients had received intravenous methylprednisolone (IVMP) and plasma exchange (PE) several times, these treatments were not sufficient to improve their symptoms. Thereafter, eculizumab was initiated between 35 and 61 days after the attack onset and partially ameliorated the symptoms in all cases. These cases suggest eculizumab as a treatment option to lessen the symptoms of severe NMOSD attacks, although the efficacy of IVMP and PE before eculizumab administration cannot be excluded.
依库珠单抗是一种抗补体C5的单克隆抗体,已被批准用于预防视神经脊髓炎谱系障碍(NMOSD)复发。尽管补体激活在NMOSD发作时会导致神经炎症和组织坏死,但关于依库珠单抗在NMOSD急性期疗效的临床报告有限。为了阐明其对NMOSD发作时临床症状的有效性,我们描述了5例NMOSD患者,他们在发作治疗后不久就接受了依库珠单抗治疗。患者包括4名女性患者和1名年龄在50 - 93岁的男性患者。首发发作3例为视神经炎,1例为脊髓炎,1例为脑干脑炎和脊髓炎。3例患者未接受任何维持治疗。尽管所有患者都多次接受了静脉注射甲泼尼龙(IVMP)和血浆置换(PE),但这些治疗不足以改善他们的症状。此后,在发作开始后35至61天开始使用依库珠单抗,所有病例的症状均得到部分改善。这些病例表明,依库珠单抗可作为减轻严重NMOSD发作症状的一种治疗选择,尽管不能排除在使用依库珠单抗之前IVMP和PE的疗效。