Hoepner Robert, Faissner Simon, Salmen Anke, Gold Ralf, Chan Andrew
Department of Neurology, St. Josef-Hospital, Ruhr-University Bochum, Germany.
J Cent Nerv Syst Dis. 2014 Apr 28;6:41-9. doi: 10.4137/JCNSD.S14049. eCollection 2014.
Natalizumab (Nat) is a humanized monoclonal antibody used for the treatment of relapsing multiple sclerosis (MS). Nat inhibits lymphocyte migration via the blood brain barrier (BBB) by blockage of an integrin adhesion molecule, very late antigen 4. During the phase III clinical trials, it was shown that Nat reduces disease activity and prevents disability progression. In addition, several smaller studies indicate a positive influence of Nat on cognition, depression, fatigue, and quality of life (Qol). Therapeutic efficacy has to be weighed against the risk of developing potentially fatal progressive multifocal leukoencephalopathy (PML), an opportunistic infection by JC-virus (JCV) with an incidence of 3.4/1000 (95% CI 3.08-3.74) in Nat treated MS patients. In this review article, we will review data on the presumed mechanism of Nat action, clinical and paraclinical efficacy parameters, and adverse drug reactions with a special focus on PML.
那他珠单抗(Nat)是一种用于治疗复发型多发性硬化症(MS)的人源化单克隆抗体。那他珠单抗通过阻断整合素黏附分子——极晚期抗原4,抑制淋巴细胞通过血脑屏障(BBB)迁移。在III期临床试验中,结果表明那他珠单抗可降低疾病活动度并预防残疾进展。此外,一些规模较小的研究表明,那他珠单抗对认知、抑郁、疲劳和生活质量(Qol)有积极影响。治疗效果必须与发生潜在致命性进行性多灶性白质脑病(PML)的风险相权衡,PML是由JC病毒(JCV)引起的一种机会性感染,在接受那他珠单抗治疗的MS患者中的发生率为3.4/1000(95%CI 3.08 - 3.74)。在这篇综述文章中,我们将回顾关于那他珠单抗作用的推测机制、临床和临床前疗效参数以及药物不良反应的数据,并特别关注PML。