Greater humoral EBV response may be associated with choroid plexus inflammation in progressive MS.

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Dejan Jakimovski, Robert Zivadinov, Murali Ramanathan, Bianca Weinstock-Guttman, Eleonora Tavazzi, Michael G Dwyer, Niels Bergsland
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引用次数: 0

Abstract

Choroid plexus (CP) inflammation can be quantified in vivo with MRI in people with multiple sclerosis (pwMS). It remains unknown whether Epstein Barr Virus (EBV) is related to CP changes. Total of 170 pwMS (116 relapsing-remitting; RRMS and 54 progressive MS; PMS) underwent MRI examination and measurement of humoral anti-EBV response. CP volume and CP pseudo-T2 (pT2), a relaxation time indicative of edema and neuroinflammation, were measured. Moreover, anti-EBV nuclear antigen-1 (EBNA-1) IgG and anti-EBV capsid antigen (VCA) IgG antibodies were measured. The PMS group had greater CP pT2 value when compared to RRMS (1120ms vs. 954ms, p = 0.037). After adjusting for age and therapy effects, higher CP pT2 values were associated with higher anti-EBNA-1 IgG levels only in PMS (r = 0.352, p = 0.015). Higher Anti-EBV humoral response in pwMS may be associated with increased CP neuroinflammatory changes and may be more relevant for the later chronic stage of the disease. Large-scale studies should investigate whether these findings are generalizable to all types of progressive MS.

进行性多发性硬化症的脉络丛炎症可能与更大的体液 EBV 反应有关。
多发性硬化症患者(pwMS)的脉络丛(CP)炎症可通过核磁共振成像进行活体量化。目前尚不清楚爱泼斯坦巴氏病毒(EBV)是否与CP变化有关。共有 170 名多发性硬化症患者(116 名复发缓解型多发性硬化症患者(RRMS)和 54 名进行性多发性硬化症患者(PMS))接受了核磁共振成像检查和体液抗 EBV 反应测量。测量了CP体积和CP假T2(pT2),假T2是表示水肿和神经炎症的弛豫时间。此外,还测量了抗EBV核抗原-1(EBNA-1)IgG和抗EBV囊抗原(VCA)IgG抗体。与 RRMS 相比,PMS 组的 CP pT2 值更高(1120ms 对 954ms,p = 0.037)。在对年龄和治疗效果进行调整后,只有PMS组较高的CP pT2值与较高的抗EBNA-1 IgG水平相关(r = 0.352,p = 0.015)。pwMS 中较高的抗 EBV 体液反应可能与 CP 神经炎症变化的增加有关,并且可能与疾病的后期慢性阶段更为相关。大规模研究应探讨这些发现是否适用于所有类型的进行性多发性硬化症。
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来源期刊
Journal of NeuroVirology
Journal of NeuroVirology 医学-病毒学
CiteScore
6.60
自引率
3.10%
发文量
77
审稿时长
6-12 weeks
期刊介绍: The Journal of NeuroVirology (JNV) provides a unique platform for the publication of high-quality basic science and clinical studies on the molecular biology and pathogenesis of viral infections of the nervous system, and for reporting on the development of novel therapeutic strategies using neurotropic viral vectors. The Journal also emphasizes publication of non-viral infections that affect the central nervous system. The Journal publishes original research articles, reviews, case reports, coverage of various scientific meetings, along with supplements and special issues on selected subjects. The Journal is currently accepting submissions of original work from the following basic and clinical research areas: Aging & Neurodegeneration, Apoptosis, CNS Signal Transduction, Emerging CNS Infections, Molecular Virology, Neural-Immune Interaction, Novel Diagnostics, Novel Therapeutics, Stem Cell Biology, Transmissable Encephalopathies/Prion, Vaccine Development, Viral Genomics, Viral Neurooncology, Viral Neurochemistry, Viral Neuroimmunology, Viral Neuropharmacology.
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