Warnke Clemens, Menge Til, Hartung Hans-Peter, Racke Michael K, Cravens Petra D, Bennett Jeffrey L, Frohman Elliot M, Greenberg Benjamin M, Zamvil Scott S, Gold Ralf, Hemmer Bernhard, Kieseier Bernd C, Stüve Olaf
Neurology Section, VA North Texas Health Care System, Medical Service, 4500 S Lancaster Rd, Dallas, TX 75216, USA.
Arch Neurol. 2010 Aug;67(8):923-30. doi: 10.1001/archneurol.2010.161.
Natalizumab (Tysabri) was the first monoclonal antibody approved for the treatment of relapsing forms of multiple sclerosis (MS). After its initial approval, 3 patients undergoing natalizumab therapy in combination with other immunoregulatory and immunosuppressive agents were diagnosed with progressive multifocal leukoencephalopathy (PML). The agent was later reapproved and its use restricted to monotherapy in patients with relapsing forms of MS. Since reapproval in 2006, additional cases of PML were reported in patients with MS receiving natalizumab monotherapy. Thus, there is currently no convincing evidence that natalizumab-associated PML is restricted to combination therapy with other disease-modifying or immunosuppressive agents. In addition, recent data indicate that risk of PML might increase beyond 24 months of treatment.
那他珠单抗(泰萨比)是首个被批准用于治疗复发型多发性硬化症(MS)的单克隆抗体。在其首次获批后,3名接受那他珠单抗治疗并联合其他免疫调节和免疫抑制药物的患者被诊断出患有进行性多灶性白质脑病(PML)。该药物后来再次获批,其使用仅限于复发型MS患者的单一疗法。自2006年再次获批以来,接受那他珠单抗单一疗法的MS患者中又报告了多例PML病例。因此,目前没有令人信服的证据表明与那他珠单抗相关的PML仅限于与其他疾病改善或免疫抑制药物联合治疗。此外,最近的数据表明,PML的风险可能在治疗超过24个月后增加。