Department of Neuroradiology, IRCCS San Raffaele Hospital, Milan, Italy.
Multiple Sclerosis Center, ASST Spedali Civili di Brescia, Brescia, Italy.
Mult Scler. 2019 Jul;25(8):1196-1201. doi: 10.1177/1352458519832259. Epub 2019 Apr 9.
A 31-year-old woman affected by multiple sclerosis (MS) experienced generalized tonic-clonic seizures 2 months after the second alemtuzumab cycle. Positive JC virus (JCV)-DNA in cerebrospinal fluid (CSF) and lesion iconography at magnetic resonance imaging (MRI) were suggestive of progressive multifocal leukoencephalopathy (PML). After 1 month, during full-blown immune reconstitution inflammatory syndrome, JCV-DNA became negative and symptoms gradually improved. New T- and B-cell output and T- and B-cell diversity were low and lymphocytes poorly responded to stimulation. This is the first case of an alemtuzumab-treated patient with clinical symptoms and radiological features compatible with PML. The lack of large T- and B-cell diversity, necessary for JCV recognition, is likely to have concurred to PML insurgence.
一位 31 岁的多发性硬化症(MS)女性患者,在接受第二次阿仑单抗治疗周期后 2 个月出现全身性强直阵挛性癫痫发作。脑脊液(CSF)中 JC 病毒(JCV)-DNA 阳性和磁共振成像(MRI)上的病变影像学提示进行性多灶性脑白质病(PML)。1 个月后,在完全免疫重建炎症综合征期间,JCV-DNA 转为阴性,症状逐渐改善。新的 T 细胞和 B 细胞输出以及 T 细胞和 B 细胞多样性较低,淋巴细胞对刺激反应不佳。这是首例阿仑单抗治疗的患者出现与 PML 相符的临床症状和影像学特征。缺乏识别 JCV 所需的大量 T 细胞和 B 细胞多样性,可能是导致 PML 发作的原因。