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自身免疫性脑病和痴呆的免疫疗法。

Immunotherapeutics for autoimmune encephalopathies and dementias.

机构信息

College of Medicine, Mayo Clinic, 200 1st ST SW, Rochester, MN, 55905, USA,

出版信息

Curr Treat Options Neurol. 2013 Dec;15(6):723-37. doi: 10.1007/s11940-013-0251-8.

Abstract

The timely implementation of immunotherapy is key to successful treatment of autoimmune encephalopathies or dementias (from here on will be referred to as autoimmune encephalopathies). There are different levels of diagnostic certainty which should guide the immunological treatment of autoimmune encephalopathies. There is a high level of diagnostic certainty for patients who have classic limbic encephalitis and have a neural antibody detected in serum or CSF (such as potassium channel complex antibody). For these patients, initiating high-dose corticosteroids or IVIg is indicated, with plasma exchange, rituximab or cyclophosphamide used as second-line therapy if first-line therapy proves only partially beneficial. There is a lower level of diagnostic certainty in patients with non-limbic atypical phenotypes (though rapidly progressive) when no neural antibody is detected in serum and CSF. A trial of corticosteroids or IVIg (or both sequentially) may be undertaken in these patients, but if no objective improvements occur, further immunotherapy is unlikely to be beneficial. Antiepileptic treatment also plays a critical role in those who have seizures as well as cognitive symptoms. Evaluation for and treatment of any underlying cancer is another component for those patients with a paraneoplastic cause of encephalitis. An individualized maintenance regimen needs to be designed for patients who do improve with immunotherapy. Individual factors that need to be considered when formulating a program of maintenance treatment include disease severity, antibody specificity and proclivity for disease relapse. Azathioprine and mycophenolate mofetil are frequently used for the purpose of remission maintenance, and should permit gradual withdrawal of steroids, IVIg or more toxic immunosuppressants. The duration of maintenance therapy is uncertain, but this author typically recommends 3-5 years of relapse-free maintenance treatment before discontinuing immunotherapy altogether.

摘要

及时实施免疫疗法是成功治疗自身免疫性脑病或痴呆症(以下简称自身免疫性脑病)的关键。不同的诊断确定性水平应指导自身免疫性脑病的免疫治疗。对于具有经典边缘性脑炎且血清或 CSF 中检测到神经抗体(如钾通道复合物抗体)的患者,具有高度诊断确定性。对于这些患者,建议使用大剂量皮质类固醇或 IVIg,如果一线治疗仅部分有效,则使用血浆置换、利妥昔单抗或环磷酰胺作为二线治疗。对于血清和 CSF 中未检测到神经抗体的非边缘性非典型表型(尽管进展迅速)的患者,诊断确定性较低。对于这些患者,可以尝试使用皮质类固醇或 IVIg(或两者顺序使用),但如果没有客观改善,则进一步免疫治疗可能无益。抗癫痫治疗对于有癫痫发作和认知症状的患者也起着至关重要的作用。对于那些因副肿瘤性脑炎而患有脑炎的患者,评估和治疗任何潜在的癌症也是另一个组成部分。对于那些通过免疫疗法改善的患者,需要设计个体化的维持治疗方案。在制定维持治疗方案时需要考虑的个体因素包括疾病严重程度、抗体特异性和疾病复发倾向。硫唑嘌呤和霉酚酸酯常用于缓解维持,应允许逐渐停用皮质类固醇、IVIg 或更具毒性的免疫抑制剂。维持治疗的持续时间不确定,但作者通常建议在完全停止免疫治疗之前,进行 3-5 年无复发维持治疗。

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