Inuzuka Takashi, Hayashi Yuichi, Kimura Akio
Department of Neurology & Geriatrics, Gifu University Graduate School of Medicine.
Rinsho Shinkeigaku. 2011 Nov;51(11):834-7. doi: 10.5692/clinicalneurol.51.834.
Paraneoplastic neurological syndrome (PNS) is a rare disorder caused by the remote effects of cancer and is considered as immune-responses to the molecules on cancer which cross-react with self-antigens in the nervous system. Since the 1980s, several specific anti onconeural antibodies have been reported, which are useful diagnostic markers of PNS and occult cancer. Only a few onconeural antibodies have been identified as primary effectors of neurological damage. Recently sophisticated methods for the detection of new or low titer antibodies have been developed. Several new auto-antibodies against receptors or ion channels on the surface of neuronal membrane, such as NMDA receptors, AMPA receptors, GABA(B) receptors and VGKC complexes, have been reported in the patients with encephalopathy including limbic encephalitis. These diseases can be associated with tumor, but they are more often non-paraneoplastic. These antibodies are generally good biomarkers for effective immunomodulatory treatment for immune-mediated encephalitis with not only consciousness disturbance but also dementia, seizures and psychiatric symptoms which sometimes mimic schizophrenia. Further studies are required to clarify the exact mechanisms underlying neuronal damage in immune-mediated neurological diseases including PNS, which may lead to the development of more rational therapies and greater understanding of immunology in the nervous system.
副肿瘤性神经系统综合征(PNS)是一种由癌症的远隔效应引起的罕见疾病,被认为是对癌症上与神经系统自身抗原发生交叉反应的分子的免疫反应。自20世纪80年代以来,已报道了几种特异性抗肿瘤神经抗体,它们是PNS和隐匿性癌症的有用诊断标志物。只有少数肿瘤神经抗体被确定为神经损伤的主要效应物。最近,已开发出检测新的或低滴度抗体的精密方法。在包括边缘性脑炎在内的脑病患者中,已报道了几种针对神经元膜表面受体或离子通道的新自身抗体,如N-甲基-D-天冬氨酸(NMDA)受体、α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体、γ-氨基丁酸B(GABA(B))受体和电压门控钾通道(VGKC)复合物。这些疾病可能与肿瘤有关,但更常见的是非副肿瘤性的。这些抗体通常是有效的免疫调节治疗的良好生物标志物,用于治疗不仅有意识障碍,还伴有痴呆、癫痫和精神症状(有时类似精神分裂症)的免疫介导性脑炎。需要进一步研究以阐明包括PNS在内的免疫介导性神经疾病中神经元损伤的确切机制,这可能会导致开发更合理的治疗方法,并加深对神经系统免疫学的理解。