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在治疗难治性抗NMDAR脑炎中成功联合靶向B细胞和浆细胞。

Successful combined targeting of B- and plasma cells in treatment refractory anti-NMDAR encephalitis.

作者信息

Sveinsson Olafur, Granqvist Mathias, Forslin Yngve, Blennow Kaj, Zetterberg Henrik, Piehl Fredrik

机构信息

Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Department of Neurology, Karolinska University Hospital, Stockholm, Sweden.

Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden; Department of Neurology, Karolinska University Hospital, Stockholm, Sweden.

出版信息

J Neuroimmunol. 2017 Nov 15;312:15-18. doi: 10.1016/j.jneuroim.2017.08.011. Epub 2017 Aug 25.

Abstract

We describe an extremely severe case of therapy refractory NMDA receptor encephalitis (NMDAe) in a 26-year-old woman. After rituximab, bilateral oophorectomy, repeated cycles of high dose methylprednisolone and plasma exchange, she received repeated cyclophosphamide, tocilizumab (interleukin-6 inhibitor) and finally bortezomib (plasma cell depleting drug) leading to remission after 204days in intensive care. Two years after disease onset her cognitive functions are still affected, but slowly improving and the cerebral atrophy has been partly reversed. The cerebrospinal fluid biomarker profile suggests an early synaptic/dendritic process, with subsequent neuroaxonal degeneration motivating aggressive treatment early on.

摘要

我们描述了一名26岁女性患有极其严重的难治性N-甲基-D-天冬氨酸受体脑炎(NMDAe)的病例。在接受利妥昔单抗、双侧卵巢切除术、多次大剂量甲基强的松龙和血浆置换治疗后,她又接受了多次环磷酰胺、托珠单抗(白细胞介素-6抑制剂)治疗,最后接受硼替佐米(浆细胞清除药物)治疗,在重症监护204天后病情缓解。发病两年后,她的认知功能仍受影响,但正在缓慢改善,脑萎缩也已部分逆转。脑脊液生物标志物谱表明早期存在突触/树突过程,随后出现神经轴突退变,这促使早期进行积极治疗。

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