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首页> 外文期刊>Frontiers in Neurology >Commentary: Detection Methods for Autoantibodies in Suspected Autoimmune Encephalitis
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Commentary: Detection Methods for Autoantibodies in Suspected Autoimmune Encephalitis

机译:评论:疑似自身免疫性脑炎中自身抗体的检测方法

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In their paper, Recken and colleagues, review the different autoantibodies, related clinical presentations and cancer associations and detection methods for autoantibodies. The review was comprehensive and nicely described most of the established antibodies. However, when discussing paraneoplastic associated antibodies, the authors failed to mention Purkinje cell antibody type 2 (PCA-2) which is a well-established paraneoplastic antibody ( 1 ). PCA-2 has first been described in 2000 by Vernino and Lennon ( 2 ) that reported 10 patients with diverse clinical presentations of which 80% had lung cancer. Recently it was discovered that this antibody targets the microtubule associated protein 1B (MAP1B) ( 3 ). MAP1B is a part of the microtubule associated protein family that also includes MAP1 (A and B), MAP2 (A and B), and tau protein. These proteins bind and stabilize microtubules. MAP1B expression peaks during early stages of neuronal development and plays an important role in neuronal differentiation, including dendritic spine formation and synaptic maturation ( 4 ). In this recent paper, describing 118 patients, PCA-2 was shown to be as common as anti amphiphysin IgG and more common than ANNA-2 (also known as anti-Ri) and PCA-Tr (also known as deltaotch-like epidermal growth factor-related receptor [DNER]). PCA-2 positivity was associated with cancer in 79% of the patients, with the majority being small cell lung cancer (SCLC) ( 3 ). The clinical presentation among patients varied and included peripheral neuropathy, 53%; cerebellar ataxia, dysmetria, or dysarthria, 38%; and encephalopathy, 27%. Ophthalmologic and spinal involvements were also reported. MAP1B was shown to present in SCLC as well as in the brain which further support it as a paraneoplastic marker. The fact that PCA-2 is not yet available in commercial kits, might mistakenly rule out the diagnosis of a paraneoplastic neurological syndrome. This makes including PCA-2 in such a review even more important so it will remain in the differential diagnosis in cases the available commercial kits are negative. In such cases it is important to seek for cancer and if possible use immuno-fluorescence assays available for PCA-2 detection. Author Contributions The author confirms being the sole contributor of this work and has approved it for publication. Conflict of Interest Statement The author published a paper in which MAP1B was described as the antigen of PCA-2. The author is a part of the group that holds a patent on MAP1B as a marker for SCLC and paraneoplastic neurological autoimmunity – patent number 2016-372.
机译:Recken及其同事在其论文中回顾了不同的自身抗体,相关的临床表现,癌症关联以及自身抗体的检测方法。该综述是全面的,并且很好地描述了大多数已建立的抗体。但是,当讨论副肿瘤相关抗体时,作者没有提及2型的Purkinje细胞抗体(PCA-2),这是一种公认​​的副肿瘤抗体(1)。 PCA-2在2000年由Vernino和Lennon(2)首次描述,该研究报告了10名具有不同临床表现的患者,其中80%患有肺癌。最近发现该抗体靶向微管相关蛋白1B(MAP1B)(3)。 MAP1B是微管相关蛋白家族的一部分,还包括MAP1(A和B),MAP2(A和B)和tau蛋白。这些蛋白质结合并稳定微管。 MAP1B表达在神经元发育的早期达到峰值,并在神经元分化(包括树突棘形成和突触成熟)中发挥重要作用(4)。在最近的描述118位患者的论文中,PCA-2被证明与抗两亲性IgG一样常见,并且比ANNA-2(也被称为抗Ri)和PCA-Tr(也被称为δ/缺口样)更为常见。表皮生长因子相关受体[DNER]。在79%的患者中,PCA-2阳性与癌症相关,大多数为小细胞肺癌(SCLC)(3)。患者的临床表现各不相同,包括周围神经病变,占53%。小脑共济失调,子宫发育不良或构音障碍38%;和脑病占27%。也有眼科和脊柱受累的报道。 MAP1B已显示出存在于SCLC以及大脑中,这进一步支持了它作为副肿瘤标记。 PCA-2尚未在商业工具包中提供,这一事实可能会错误地排除诊断副肿瘤性神经系统综合症的可能性。这样一来,将PCA-2纳入这一审查就显得尤为重要,因此,在市售试剂盒阴性的情况下,它将保留在鉴别诊断中。在这种情况下,寻找癌症非常重要,如果可能,请使用可用于PCA-2检测的免疫荧光测定法。作者贡献作者确认是该作品的唯一贡献者,并已批准将其发表。利益冲突声明作者发表了一篇论文,其中MAP1B被描述为PCA-2的抗原。作者是该小组的成员之一,该小组拥有MAP1B的专利,作为SCLC和副肿瘤神经系统自身免疫性疾病的标记物-专利号2016-372。

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