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Screening for autoantibodies in inflammatory neurological syndrome using fluorescence pattern in a tissue-based assay: Cerebrospinal fluid findings from 793 patients

抗体 星形胶质细胞 免疫荧光 自身抗体 脑脊液 抗原 少突胶质细胞 病理 免疫学 医学 多发性硬化 免疫球蛋白G 生物 中枢神经系统 内科学 髓鞘
作者
Tianni Liu,Baikeng Chen,Huacai Yang,Jiehong Huang,Si Liu,Xinguang Yang,Li Huang,Haiyan Yao,Wei Qiu,Honghua Zhuang,Youming Long,Cong Gao
出处
期刊:Multiple sclerosis and related disorders [Elsevier BV]
卷期号:28: 177-183 被引量:22
标识
DOI:10.1016/j.msard.2018.12.036
摘要

Background To evaluate indirect immunofluorescence patterns of auto-antibodies and the targeting antigens to Immunoglobulin Gs (IgGs) in the cerebrospinal fluid (CSF) by a tissue-based assay(TBA). Methods CSF samples were collected from 793 patients. Auto-antibody levels were measured via an immunofluorescence assay. Results 110 (13.9%) CSF samples with a specific response were confirmed. Of these, 37 showed a neuronal pattern, 57 an astrocyte pattern, 7 a neuronal and astrocyte pattern, and 9 samples showed an oligodendrocyte pattern. In the neuronal antibody group, 16 patients had NMDAR-IgGs, 3 had LGi1-IgGs, 2 had AMPA2-IgGs, 2 had GAD65-IgGs, 1 patient had GABA-IgGs, and 1 patient had overlapping NMDAR-IgGs and AQP4-IgGs. Of the unidentified neuronal antibodies, two were cellular surface antibodies, three were cellular surface and cytoplasm antibodies, three were cytoplasm antibodies, and four were nuclear and cytoplasm antibodies. Among the 57 patients with the astrocyte pattern, 28 patients were positive for AQP4-IgGs, 21 were positive for GFAP-IgGs, 5 patients had overlapping AQP4 and GFAP-IgGs, and 3 patients had an unidentified antigen. Seven patients showed neuronal and astrocyte patterns simultaneously; four of them had unknown neuronal antibodies. In the patients with an oligodendrocyte pattern, one was positive for MOG-IgGs and four for MBP-IgGs. Conclusions The TBA is helpful for diagnosing autoimmune neurological syndrome, especially in patients with unknown antibodies and antigens. Presence of unidentified antibodies against neuronal or glial cells could be an interesting finding, but should be investigated in future studies which incorporate parallel serum samples at an appropriate IgG dilution.
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