Ohtomo Takayuki, Ogino Sakura, Yanai Sayaka, Nakayama Sayaka, Yajima Risa, Sugawara Mayu, Yamada Junji, Aizawa Hitoshi, Taguchi Takeshi, Nanri Kazunori
Center for Clinical Pharmacy, Tokyo University of Pharmacy and Life Sciences.
Department of Neurology, Tokyo Medical University.
Rinsho Shinkeigaku. 2022 Feb 19;62(2):112-122. doi: 10.5692/clinicalneurol.cn-001621. Epub 2022 Jan 31.
Autoimmune cerebellar ataxia (AICA) is a general term for diseases in which the cerebellum is damaged by an autoimmune mechanism. For the diagnosis of the AICA, anti-thyroid antibodies (anti-thyroid peroxidase antibody and anti-thyroglobulin antibody), anti-glutamic acid decarboxylase (GAD) antibodies, and anti-gliadin antibodies are measured. Immunotherapy is known to be effective for AICA, but some patients with effective immunotherapy lack autoantibodies associated with cerebellar ataxia. The purpose of this study was to clarify whether the effectiveness of immunotherapy in patients with suspected AICA could be predicted by anti-mouse cerebellar tissue-derived antigen antibody tests.
This study was conducted on 25 patients with idiopathic cerebellar ataxia (excluding multiple system atrophy, hereditary spinocerebellar degeneration, cancer-bearing patients, and patients taking phenytoin) who received immunotherapy from 2005 to 2016 at Tokyo Medical University Hachioji Medical Center. The patients were suspected of having AICA because they were positive for cerebellar ataxia-related autoantibodies (anti-thyroid antibody, anti-GAD antibody, anti-gliadin antibody, or anti-transglutaminase 6 antibody) or other autoantibodies. Antibodies that bind to mouse cerebellar tissue-derived antigens were defined as "anti-mouse cerebellar tissue-derived antigen antibodies" in this study, and their IgG-class antibodies were comprehensively measured using a slot blot.
Anti-mouse cerebellar tissue-derived antigen antibody test results were correlated with immunotherapy efficacy. Furthermore, the combination of anti-mouse cerebellar tissue-derived antigen and anti-GAD antibody tests could predict the effectiveness of immunotherapy with 83% sensitivity and 100% specificity, while the combination of the anti-mouse cerebellar tissue-derived antigen, anti-GAD, and anti-gliadin (IgA class) antibody tests could predict the effectiveness of immunotherapy with 94% sensitivity and 86% specificity.
Anti-mouse cerebellar tissue-derived antigen antibody tests could help to provide useful information for immunotherapy administration to patients with idiopathic cerebellar ataxia suspected to be AICA.
自身免疫性小脑共济失调(AICA)是一类因自身免疫机制导致小脑受损的疾病的统称。对于AICA的诊断,需检测抗甲状腺抗体(抗甲状腺过氧化物酶抗体和抗甲状腺球蛋白抗体)、抗谷氨酸脱羧酶(GAD)抗体以及抗麦胶蛋白抗体。已知免疫疗法对AICA有效,但部分接受有效免疫疗法的患者缺乏与小脑共济失调相关的自身抗体。本研究旨在明确抗小鼠小脑组织衍生抗原抗体检测能否预测疑似AICA患者免疫疗法的疗效。
本研究纳入了2005年至2016年在东京医科大学八王子医疗中心接受免疫疗法的25例特发性小脑共济失调患者(排除多系统萎缩、遗传性脊髓小脑变性、癌症患者以及服用苯妥英的患者)。这些患者因小脑共济失调相关自身抗体(抗甲状腺抗体、抗GAD抗体、抗麦胶蛋白抗体或抗转谷氨酰胺酶6抗体)或其他自身抗体呈阳性而疑似患有AICA。在本研究中,与小鼠小脑组织衍生抗原结合的抗体被定义为“抗小鼠小脑组织衍生抗原抗体”,并使用狭缝印迹法综合检测其IgG类抗体。
抗小鼠小脑组织衍生抗原抗体检测结果与免疫疗法疗效相关。此外,抗小鼠小脑组织衍生抗原与抗GAD抗体检测联合可预测免疫疗法的有效性,敏感性为83%,特异性为100%;而抗小鼠小脑组织衍生抗原、抗GAD和抗麦胶蛋白(IgA类)抗体检测联合可预测免疫疗法的有效性,敏感性为94%,特异性为86%。
抗小鼠小脑组织衍生抗原抗体检测有助于为疑似AICA的特发性小脑共济失调患者的免疫疗法实施提供有用信息。