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病例报告:两例同时存在 MO G 抗体相关疾病和潜伏性感染的病例。

Case report: Concurrent MOG antibody-associated disease and latent infections in two patients.

机构信息

Department of Neurology and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University of Basel, Basel, Switzerland.

Departments of Biomedicine and Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.

出版信息

Front Immunol. 2024 Sep 4;15:1455355. doi: 10.3389/fimmu.2024.1455355. eCollection 2024.

Abstract

OBJECTIVES

Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) is frequently preceded by infections. The underlying pathomechanism, however, remains poorly understood. Here, we present the clinical data of two MOGAD patients with concurrent syphilis infection and investigate the reactivity of patient-derived antibodies to MOG and ().

METHODS

Longitudinal serum samples and soluble immunoglobulins in single B cell supernatants were measured for MOG reactivity by a live cell-based assay. Reactivity against was assessed by enzyme-linked immunosorbent assay.

RESULTS

The two patients presented MOGAD and concurrent latent syphilis infection, manifesting as cervical myelitis and unilateral optic neuritis, respectively. The first patient had been living with HIV on antiretroviral therapy, and the second was concomitantly diagnosed with chronic hepatitis B infection. Upon screening of B cell supernatants, we identified reactivity to MOG or Notably, one B cell showed reactivity to both antigens.

DISCUSSION

The coexistence of MOGAD diagnoses and latent syphilis, alongside the identification of antibody reactivity to MOG and , underscores the potential pathomechanistic link between syphilis infection and subsequent autoimmune neuroinflammation. Cross-reactivity between MOG and antibodies remains to be validated on a molecular level, and further characterization of infectious triggers associated with MOGAD is needed.

摘要

目的

髓鞘少突胶质细胞糖蛋白(MOG)抗体相关疾病(MOGAD)常以前驱感染为特征。然而,其潜在的发病机制仍知之甚少。在此,我们报告 2 例并发梅毒感染的 MOGAD 患者的临床资料,并探讨了患者来源的抗体对 MOG 和 ()的反应性。

方法

通过活细胞检测,测量 MOG 反应性的纵向血清样本和单个 B 细胞上清液中的可溶性免疫球蛋白。通过酶联免疫吸附试验评估针对 的反应性。

结果

这 2 名患者均表现为 MOGAD 和潜伏性梅毒感染,分别表现为颈髓炎和单侧视神经炎。第 1 例患者在接受抗逆转录病毒治疗的同时患有 HIV,第 2 例患者同时被诊断为慢性乙型肝炎感染。在筛选 B 细胞上清液时,我们发现对 MOG 或 有反应性。值得注意的是,有一个 B 细胞对这两种抗原均有反应性。

讨论

MOGAD 诊断与潜伏性梅毒共存,以及对 MOG 和 抗体的反应性鉴定,突出了梅毒感染与随后的自身免疫性神经炎症之间潜在的发病机制联系。MOG 和 抗体之间的交叉反应性尚需在分子水平上进行验证,并且需要进一步描述与 MOGAD 相关的感染触发因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f88/11408232/b9609125dc96/fimmu-15-1455355-g001.jpg

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