Center for Crohn's and Colitis, Department of Gastroenterology, Kyung Hee University Hospital, Kyung Hee University College of Medicine, Seoul, South Korea.
Department of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea.
Front Immunol. 2022 Oct 31;13:957575. doi: 10.3389/fimmu.2022.957575. eCollection 2022.
Infliximab, a chimeric monoclonal antibody against anti-tumor necrosis factor-α (TNF-α), has revolutionized the management of inflammatory bowel disease. However, a recent nested case-control study showed that anti-TNF-α therapy exposure in patients with autoimmune diseases is associated with an increased risk of inflammatory central nervous system (CNS) events. A 27-year-old man diagnosed with Crohn's disease at 17 years of age was referred to our clinic for suffering with Wernicke's aphasia and the right-hand weakness over two weeks. Nine years of treatment for Crohn's disease with infliximab anti-TNF-α therapy was well tolerated. An initial MRI revealed diffuse leptomeningeal enhancement along the bilateral cerebral sulci without any parenchymal abnormalities. Cerebrospinal fluid (CSF) and serum N-methyl-D-aspartate receptor (NMDAR) antibody testing yielded positive results. Anti-NMDAR encephalitis was diagnosed, and the patient was treated with rituximab. A follow-up brain MRI showed new multiple cerebral lesions in the left insular cortex and subcortical white matter of the left frontal and temporal gyri. Approximately 8 months after symptom onset, the CSF and serum NMDAR antibody converted to negative. Twelve months later, the patient fully recovered from anti-NMDAR encephalitis without any neurological deficits and is currently being treated with the anti-interleukin 12/23 agent ustekinumab for Crohn's disease. This is the first report of not only a patient with infliximab-associated anti-NMDAR encephalitis in Crohn's disease but also of an inflammatory non-demyelinating CNS event during long-term suppression of TNF-α. Our case highlights the need for clinicians to recognize the possibility of a paradoxical autoimmune response occurring with novel biological therapies.
英夫利昔单抗是一种针对肿瘤坏死因子-α(TNF-α)的嵌合单克隆抗体,它彻底改变了炎症性肠病的治疗方法。然而,最近一项巢式病例对照研究表明,自身免疫性疾病患者接受抗 TNF-α 治疗与炎症性中枢神经系统(CNS)事件的风险增加相关。
一名 27 岁男性,17 岁时被诊断患有克罗恩病,因两周来出现韦尼克失语症和右手无力而被转至我科就诊。该患者接受英夫利昔单抗抗 TNF-α 治疗 9 年,病情一直得到很好的控制。最初的 MRI 显示双侧大脑脑沟弥漫性脑膜增强,无任何实质异常。脑脊液(CSF)和血清 N-甲基-D-天冬氨酸受体(NMDAR)抗体检测结果均为阳性。诊断为抗 NMDAR 脑炎,给予利妥昔单抗治疗。随访脑 MRI 显示左侧岛叶皮质和左侧额颞叶皮质下白质出现新的多发性脑病变。症状出现约 8 个月后,CSF 和血清 NMDAR 抗体转为阴性。12 个月后,患者完全从抗 NMDAR 脑炎中康复,无任何神经功能缺损,目前正在接受抗白细胞介素 12/23 制剂乌司奴单抗治疗克罗恩病。这是首例报告既患有克罗恩病相关的英夫利昔单抗相关抗 NMDAR 脑炎,又患有 TNF-α 长期抑制后炎症性非脱髓鞘性 CNS 事件的患者。我们的病例强调了临床医生需要认识到新型生物疗法可能会出现矛盾的自身免疫反应。