Stüve Olaf, Marra Christina M, Cravens Petra D, Singh Mahendra P, Hu Wei, Lovett-Racke Amy, Monson Nancy L, Phillips J Theodore, Tervaert Jan W Cohen, Nash Richard A, Hartung Hans-Peter, Kieseier Bernd C, Racke Michael M, Frohman Elliot M, Hemmer Bernhard
Neurology Section, Medical Service, Veterans Affairs North Texas Health Care System, Dallas, TX, USA.
Arch Neurol. 2007 Feb;64(2):169-76. doi: 10.1001/archneur.64.2.169.
Natalizumab (Tysabri) is an effective therapy for multiple sclerosis. Recently, 3 patients who were treated with natalizumab developed progressive multifocal leukoencephalopathy (PML), an opportunistic infection of the brain with the polyomavirus JC. The pathogenesis of natalizumab-associated PML may be different from that of PML not associated with the drug. We reviewed biologically feasible interventions for patients diagnosed as having PML or other infections while receiving natalizumab therapy. Existing interventions include antiviral treatment, immunomodulatory therapies, hematopoietic growth factors, plasma exchange, intravenous immunoglobulins, and leukapheresis and autotransfusion of leukocytes. In addition, we examined the feasibility of experimental therapies, including small interfering RNA, the in vivo use of antiserum, and recombinant natalizumab-blocking molecules. There is only circumstantial evidence that any of the proposed treatments will benefit patients with multiple sclerosis treated with natalizumab who may develop PML. In addition, the expected incidence of PML in this patient population will likely be too low to test any of the proposed interventions in a controlled manner. Because it is currently impossible to identify patients at risk, and thus to prevent PML as a consequence of natalizumab therapy, it is important that neurologists be aware of possible therapeutic interventions.
那他珠单抗(泰萨比)是治疗多发性硬化症的一种有效疗法。最近,3名接受那他珠单抗治疗的患者发生了进行性多灶性白质脑病(PML),这是一种由多瘤病毒JC引起的脑部机会性感染。那他珠单抗相关PML的发病机制可能与非药物相关的PML不同。我们回顾了针对在接受那他珠单抗治疗时被诊断患有PML或其他感染的患者的生物学可行干预措施。现有的干预措施包括抗病毒治疗、免疫调节疗法、造血生长因子、血浆置换、静脉注射免疫球蛋白以及白细胞单采和白细胞自体输血。此外,我们研究了实验性疗法的可行性,包括小干扰RNA、抗血清的体内应用以及重组那他珠单抗阻断分子。仅有间接证据表明任何一种提议的治疗方法会使接受那他珠单抗治疗且可能发生PML的多发性硬化症患者受益。此外,该患者群体中PML的预期发病率可能过低,无法以对照方式测试任何一种提议的干预措施。由于目前无法识别有风险的患者,从而预防那他珠单抗治疗导致的PML,因此神经科医生了解可能的治疗干预措施很重要。