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抗 EBNA1 IgG 效价与多发性硬化症患者的疲劳无关。

Anti-EBNA1 IgG titre is not associated with fatigue in multiple sclerosis patients.

机构信息

Department of Neurology, University Medicine Essen, Essen, Germany.

Centre for Translational Neuro- and Behavioural Sciences (C-TNBS), University Medicine Essen, Essen, Germany.

出版信息

Neurol Neurochir Pol. 2022;56(3):236-245. doi: 10.5603/PJNNS.a2022.0043. Epub 2022 Jun 21.

Abstract

INTRODUCTION

Fatigue is the most frequent symptom in multiple sclerosis (MS), although it is still poorly understood due to its complexity and subjective nature. There is an urgent need to identify reliable biomarkers to improve disease prognosis and therapeutic strategies. Epstein-Barr virus (EBV) is the major environmental risk factor associated with MS aetiology, and trials with EBV-targeted T cell therapies have reduced fatigue severity in MS patients.

AIM OF THE STUDY

We investigated whether the serum amount of immunoglobulin (Ig)G-specific for EBV antigens could be a suitable prognostic marker for the assessment of MS-related fatigue.

MATERIAL AND METHODS

A total of 194 MS patients were enrolled. We quantified EBV nuclear antigen 1 (EBNA1) and EBV viral capsid antigen (VCA) immunoglobulin (Ig) G levels and B cell-activating factor of the tumour necrosis factor family (BAFF) concentration in the serum of patients with relapsing-remitting MS (RRMS) and chronic progressive MS (CPMS), and we analysed their correlation with aspects of fatigue and other clinical disease parameters.

RESULTS

A complete EBV seropositivity could be detected in our cohort. After adjusting for confounding variables and covariates, neither EBNA1 nor VCA antibody titres were associated with levels of fatigue, sleepiness, depression, or with any of the clinical values such as expanded disability status scale, lesion count, annual relapse rate, or disease duration. However, patients with RRMS had significantly higher EBNA1 IgG titre than those with CPMS, whereas this was not the case under therapies targeting CD20+ cells. BAFF levels in serum were inversely proportional to anti-EBNA1 IgG.

CONCLUSIONS AND CLINICAL IMPLICATIONS

Our results show that EBNA1 IgG titre is not associated with the presence or level of fatigue. Whether the increased EBNA1 titre in RRMS plays a direct role in disease progression, or is only a consequence of excessive B cell activation, remains to be answered in future studies.

摘要

简介

疲劳是多发性硬化症(MS)最常见的症状,但由于其复杂性和主观性,仍未得到充分理解。目前迫切需要确定可靠的生物标志物,以改善疾病预后和治疗策略。EB 病毒(EBV)是与 MS 病因学相关的主要环境风险因素,针对 EBV 靶向 T 细胞疗法的试验已降低了 MS 患者的疲劳严重程度。

研究目的

我们研究了针对 EBV 抗原的 IgG 特异性血清量是否可作为评估 MS 相关疲劳的合适预后标志物。

材料和方法

共纳入 194 例 MS 患者。我们定量检测了缓解-复发型 MS(RRMS)和慢性进展型 MS(CPMS)患者血清中的 EBV 核抗原 1(EBNA1)和 EBV 病毒衣壳抗原(VCA)IgG 水平以及肿瘤坏死因子家族 B 细胞激活因子(BAFF)浓度,并分析了它们与疲劳和其他临床疾病参数的相关性。

结果

我们的队列可检测到完整的 EBV 血清阳性。在调整混杂变量和协变量后,EBNA1 或 VCA 抗体滴度均与疲劳、嗜睡、抑郁水平或扩展残疾状况量表、病灶计数、年复发率或疾病持续时间等任何临床值均无相关性。然而,RRMS 患者的 EBNA1 IgG 滴度明显高于 CPMS 患者,但针对 CD20+细胞的治疗则不然。血清中 BAFF 水平与抗-EBNA1 IgG 呈反比。

结论和临床意义

我们的结果表明,EBNA1 IgG 滴度与疲劳的存在或程度无关。RRMS 中 EBNA1 滴度增加是否直接导致疾病进展,还是仅仅是过度 B 细胞激活的结果,仍有待未来研究回答。

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