Case report: Breaking CNS immuno-privilege: TNFα-inhibitor triggers aseptic meningitis in a patient with rheumatoid arthritis

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Benedetta Kassabian, Monica Facco, Alessandro Miscioscia, Samuela Carraro, Francesca Rinaldi, Paolo Gallo, Marco Puthenparampil
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引用次数: 0

Abstract

Blood-brain barrier dysfunction might be driven by peripheral inflammation. TNFα inhibitors (TNF-αi) are occasionally associated with a wide spectrum of neurological immuno-mediated disorders. However, patients with systemic autoimmune disorders, including rheumatoid arthritis (RA), might be prone to develop further organ-specific, including central nervous system (CNS), autoimmunity. Here we report the case of a patient, affected by RA and treated with etanercept, who suddenly developed focal neurological symptoms. Cerebrospinal fluid, magnetic resonance imaging (MRI), and positron emission tomography (PET)/MRI findings are reported and support the diagnosis of TNF-αi -associated aseptic meningitis.
病例报告:打破中枢神经系统免疫特权:TNFα 抑制剂引发类风湿性关节炎患者无菌性脑膜炎
血脑屏障功能障碍可能是由外周炎症引起的。TNFα 抑制剂(TNF-αi)偶尔会与多种神经系统免疫介导疾病相关。然而,包括类风湿性关节炎(RA)在内的全身性自身免疫性疾病患者可能容易进一步发展为器官特异性自身免疫,包括中枢神经系统(CNS)自身免疫。在此,我们报告了一例受类风湿关节炎影响并接受依那西普治疗的患者突然出现局灶性神经系统症状的病例。报告的脑脊液、磁共振成像(MRI)和正电子发射断层扫描(PET)/MRI结果支持TNF-αi相关性无菌性脑膜炎的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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