Anti-GluK2 Encephalitis in an Asian Child: A Case Report and Literature Review.

IF 6.2 Q1 IMMUNOLOGY
ImmunoTargets and Therapy Pub Date : 2024-12-17 eCollection Date: 2024-01-01 DOI:10.2147/ITT.S498345
Shimeng Chen, Miriam Kessi, Fang He, Fei Yin, Jing Peng, Lifen Yang
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引用次数: 0

Abstract

Background: Anti-glutamate kainate receptor subunit 2 (anti-GluK2) antibodies mediated encephalitis is very rare in both children and adults. This study aimed to describe the second report of the anti-GluK2 encephalitis worldwide, the first youngest patient worldwide, and the first case ever in Asia. Besides, this study provides a summary of the clinical manifestations of all previous reported cases.

Methods: The patient was attended at the Department of Pediatrics, Xiangya Hospital, Central South University. Anti-GluK2 antibodies were tested in the serum and cerebrospinal fluid (CSF) by the indirect immunofluorescence on cell-based assays. The clinical information of the patient was collected. In addition, a literature search was carried out in the PubMed.

Results: Our patient was a male who presented with lethargy, recurrent dizziness and vomiting, headache and cerebellar ataxia at the age of 13 years. Prodromal illnesses included Herpes Zoster infection and Mycoplasma pneumonia. The anti-GluK2 antibodies and elevated IL-6 levels were detected in serum while high oligoclonal bands levels were found in the CSF. The intravenous methylprednisolone, immunoglobulin, antibiotics and other symptomatic treatments helped the patient to recover full. We could only find one previous report in the literature (from Barcelona). The literature review plus our report unveiled eight patients with pure anti-GluK2 antibodies related encephalitis. The median age of onset was 28.50 years and majority were males (75.00%). Most of the cases (87.50%) presented with acute cerebellitis symptoms and signs. Preceding or concurrent infection was observed in two patients, while paraneoplastic tumors were observed in two patients. Patients had non-parenchymal brain lesions; the commonest anomalies were those localized in the cerebellum (62.50%).

Conclusion: Our report provides more evidence that anti-GluK2 antibodies may be pathogenic for the autoimmune encephalitis (cerebellitis). Immunotherapy can be used to treat it with good outcome.

亚洲儿童抗gluk2脑炎1例报告及文献复习。
背景:抗谷氨酸盐受体亚单位2(抗gluk2)抗体介导的脑炎在儿童和成人中都非常罕见。本研究旨在描述全球第二例抗gluk2脑炎报告,全球第一例最年轻患者,亚洲首例病例。此外,本研究总结了以往所有报告病例的临床表现。方法:患者在中南大学湘雅医院儿科就诊。采用细胞间接免疫荧光法检测血清和脑脊液中gluk2抗体。收集患者的临床资料。此外,在PubMed中进行文献检索。结果:患者为男性,13岁时出现嗜睡、反复头晕呕吐、头痛和小脑性共济失调。前驱疾病包括带状疱疹感染和肺炎支原体。血清中检测到抗gluk2抗体和IL-6水平升高,脑脊液中检测到高低克隆带水平。静脉注射甲基强的松龙、免疫球蛋白、抗生素等对症治疗使患者完全康复。我们只能在文献中找到一个先前的报告(来自巴塞罗那)。文献回顾加上我们的报告揭示了8例纯抗gluk2抗体相关脑炎患者。中位发病年龄28.50岁,以男性居多(75.00%)。绝大多数病例(87.50%)表现为急性小脑炎症状和体征。2例患者有既往感染或并发感染,2例患者有副肿瘤。患者有非脑实质病变;最常见的异常是局限于小脑(62.50%)。结论:本报告提供了更多证据,证明抗gluk2抗体可能是自身免疫性脑炎(小脑炎)的致病性。免疫疗法可用于治疗,效果良好。
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来源期刊
CiteScore
16.50
自引率
0.00%
发文量
7
审稿时长
16 weeks
期刊介绍: Immuno Targets and Therapy is an international, peer-reviewed open access journal focusing on the immunological basis of diseases, potential targets for immune based therapy and treatment protocols employed to improve patient management. Basic immunology and physiology of the immune system in health, and disease will be also covered.In addition, the journal will focus on the impact of management programs and new therapeutic agents and protocols on patient perspectives such as quality of life, adherence and satisfaction.
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