Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, Guangzhou, People's Republic of China.
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, People's Republic of China; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, National Key Clinical Department and Key Discipline of Neurology, Guangzhou, People's Republic of China.
J Neuroimmunol. 2024 Nov 15;396:578458. doi: 10.1016/j.jneuroim.2024.578458. Epub 2024 Sep 11.
Rituximab is recommended as the preferred second-line immunotherapy for autoimmune encephalitis (AE). However, Ofatumumab (OFA), a novel fully human anti-CD20 antibody, has been reported infrequently in patients with AE. Among the various forms of AE, anti-N-methyl-d-aspartate receptor (anti-NMDAR) encephalitis is the most common and severe. This study presents three cases of severe anti-NMDAR encephalitis treated with OFA following the failure of first-line immunotherapy. The results indicated that the patients experienced no significant adverse reactions after receiving OFA, and their clinical symptoms improved markedly within one week of treatment. One month post-treatment with OFA, scores on the Glasgow Coma Scale (GCS) and the Barthel Index of Activities of Daily Living (Barthel-ADL) increased, while scores on the modified Rankin Scale (mRS), Clinical Assessment Scale in Autoimmune Encephalitis (CASE), and Paroxysmal Sympathetic Hyperactivity Assessment Measure (PSH-AM) decreased. During the three-month and six-month follow-up periods, patients exhibited further symptomatic improvement, suggesting that OFA is a safe and effective treatment option for anti-NMDAR encephalitis. These findings propose a novel therapeutic strategy for severe refractory anti-NMDAR encephalitis.
利妥昔单抗被推荐为自身免疫性脑炎(AE)的首选二线免疫疗法。然而,奥法木单抗(OFA),一种新型的完全人抗 CD20 抗体,在 AE 患者中报道较少。在各种形式的 AE 中,抗 N-甲基-D-天冬氨酸受体(抗 NMDAR)脑炎是最常见和最严重的。本研究报告了三例接受一线免疫治疗失败后用 OFA 治疗的严重抗 NMDAR 脑炎患者。结果表明,患者在接受 OFA 后无明显不良反应,治疗后一周内临床症状明显改善。OFA 治疗一个月后,格拉斯哥昏迷量表(GCS)和日常生活活动量表(Barthel-ADL)评分增加,而改良 Rankin 量表(mRS)、自身免疫性脑炎临床评估量表(CASE)和阵发性交感神经过度活动评估量表(PSH-AM)评分降低。在三个月和六个月的随访期间,患者表现出进一步的症状改善,表明 OFA 是抗 NMDAR 脑炎的一种安全有效的治疗选择。这些发现为严重难治性抗 NMDAR 脑炎提出了一种新的治疗策略。