Serafini Barbara, Scorsi Eleonora, Rosicarelli Barbara, Rigau Valérie, Thouvenot Eric, Aloisi Francesca
Department of Neuroscience, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Department of Pathology, Hôpital Gui de Chauliac, and Team 'Brain plasticity, Human stem cells and Glial tumors', INSERM U1051, Institute for Neurosciences, 80 avenue Augustin Fliche, 34295 Montpellier, France.
J Neuroimmunol. 2017 Jun 15;307:14-17. doi: 10.1016/j.jneuroim.2017.03.013. Epub 2017 Mar 16.
Rebound of disease activity in multiple sclerosis patients after natalizumab withdrawal is a potentially life-threatening event. To verify whether highly destructive inflammation after natalizumab withdrawal is associated with Epstein-Barr virus (EBV) reactivation in central nervous system infiltrating B-lineage cells and cytotoxic immunity, we analyzed post-mortem brain tissue from a patient who died during a fulminating MS relapse following natalizumab withdrawal. Numerous EBV infected B cells/plasma cells and CD8+ T cells infiltrated all white matter lesions; the highest frequency of EBV lytically infected cells and granzyme B+ CD8+ T cells was observed in actively demyelinating lesions. These results may encourage switching to B-cell depleting therapy after natalizumab discontinuation.
那他珠单抗停药后多发性硬化症患者疾病活动的反弹是一个潜在的危及生命的事件。为了验证那他珠单抗停药后高度破坏性炎症是否与中枢神经系统浸润B淋巴细胞系细胞中的爱泼斯坦-巴尔病毒(EBV)再激活及细胞毒性免疫相关,我们分析了一名在那他珠单抗停药后暴发性多发性硬化症复发期间死亡患者的尸检脑组织。大量EBV感染的B细胞/浆细胞和CD8+T细胞浸润了所有白质病变;在活动性脱髓鞘病变中观察到EBV裂解感染细胞和颗粒酶B+CD8+T细胞的频率最高。这些结果可能会促使在停用那他珠单抗后改用B细胞清除疗法。