Neurocenter of Southern Switzerland, Ospedale Regionale di Lugano, Via Tesserete 46, 6903 Lugano, Switzerland.
Institute for Research in Biomedicine, Università della Svizzera italiana, 6500 Bellinzona, Switzerland.
Mult Scler Relat Disord. 2020 May;40:101927. doi: 10.1016/j.msard.2020.101927. Epub 2020 Jan 3.
Discontinuation of disease-modifying therapy with fingolimod can lead to severe Multiple Sclerosis (MS) rebound activity; however, this phenomenon remains mechanistically incompletely understood, and the short-term impact of a therapy switch on inflammatory gene expression in T lymphocytes is unknown. We present the clinico-radiological and immunological description of a case of rebound activity after fingolimod discontinuation and switching to rituximab treatment in a relapsing-remitting MS patient. After severe rebound, a reduction in the expression of inflammatory cytokines and transcription factors was rapidly observed after administration of methylprednisolone and rituximab. Rituximab led to an effective suppression of inflammatory activity, and at least in this specific case it represented a valid switching approach after fingolimod discontinuation.
停用芬戈莫德可导致严重的多发性硬化症(MS)反弹活动;然而,这种现象在机制上仍不完全清楚,且治疗转换对 T 淋巴细胞中炎症基因表达的短期影响也未知。我们介绍了一例复发缓解型多发性硬化症患者停用芬戈莫德后出现反弹活动,并转换为利妥昔单抗治疗的临床、放射学和免疫学描述。在严重的反弹后,给予甲基强的松龙和利妥昔单抗后,迅速观察到炎症细胞因子和转录因子表达减少。利妥昔单抗可有效抑制炎症活动,至少在这个特定病例中,它是停用芬戈莫德后的一种有效转换方法。