多发性硬化症患者和对照组脑脊液和血液中的爱泼斯坦-巴氏病毒

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY Neurology® Neuroimmunology & Neuroinflammation Pub Date : 2024-05-01 Epub Date: 2024-04-12 DOI:10.1212/NXI.0000000000200226
Joonas Lehikoinen, Katariina Nurmi, Mari Ainola, Jonna Clancy, Janne K Nieminen, Lilja Jansson, Hanna Vauhkonen, Antti Vaheri, Teemu Smura, Sini M Laakso, Kari K Eklund, Pentti J Tienari
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引用次数: 0

摘要

背景和目的:爱泼斯坦-巴氏病毒(EBV)感染是多发性硬化症(MS)的一个主要危险因素。我们研究了多发性硬化症患者和对照组的脑脊液和血液中是否存在 EBV DNA。我们分析了EBV DNA在多发性硬化症患者的脑脊液中是否比在对照组中更常见,并估算了脑脊液和血液中EBV阳性B细胞的比例:45名多发性硬化症患者和45名患有其他疾病的HLA-DR15匹配对照者在诊断性腰椎穿刺时采集了CSF上清液和细胞,所有参与者均为EBV血清阳性。细胞 DNA 经针对宿主和病毒 DNA 的 Phi 聚合酶扩增,在 28 个病例和 28 个对照组中获得了代表性样本。对一部分参与者的脑脊液细胞(14 例,14 例对照组)和血液 B 细胞(10 例,10 例对照组)中未扩增的 DNA 进行了分析。对每个样本进行多次液滴数字 PCR(ddPCR)检测,以评估 EBV 阳性率的累积情况。为了检测作为活化标志的病毒 RNA,对 21 名多发性硬化症患者和 3 名对照组的血液 CD4 阳性、CD8 阳性和 CD19 阳性细胞进行了 RNA 测序:45 名多发性硬化症患者中有一人,45 名对照组中没有一人在 CSF 上清液(1 mL)中发现 EBV DNA 阳性。对 CSF 细胞 DNA 进行了 8 次独立的 ddPCR 分析:28 名多发性硬化症患者中有 18 人(64%)至少检测到一次 EBV DNA,28 名对照组中有 15 人(54%)至少检测到一次 EBV DNA(费雪检验,p = 0.59)。在连续的 ddPCR 中,累计 EBV 阳性率稳步上升至 59%,这表明如果分析更多的 DNA,所有患者的 CSF 细胞中都会出现 EBV 阳性。在 CSF 和血液中,EBV 阳性 B 细胞的估计比例均大于 1/10,000。除了内源性逆转录病毒外,我们在血液淋巴细胞亚群中没有检测到病毒 RNA:讨论:用 ddPCR 法在多发性硬化症患者和对照组的 CSF 细胞中同样可检测到 EBV-DNA,概率法表明,EBV 阳性者的真实阳性率接近 100%。EBV 阳性 B 细胞的比例似乎高于之前的估计。
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Epstein-Barr Virus in the Cerebrospinal Fluid and Blood Compartments of Patients With Multiple Sclerosis and Controls.

Background and objectives: Epstein-Barr virus (EBV) infection is a major risk factor of multiple sclerosis (MS). We examined the presence of EBV DNA in the CSF and blood of patients with MS and controls. We analyzed whether EBV DNA is more common in the CSF of patients with MS than in controls and estimated the proportions of EBV-positive B cells in the CSF and blood.

Methods: CSF supernatants and cells were collected at diagnostic lumbar punctures from 45 patients with MS and 45 HLA-DR15 matched controls with other conditions, all participants were EBV seropositive. Cellular DNA was amplified by Phi polymerase targeting both host and viral DNA, and representative samples were obtained in 28 cases and 28 controls. Nonamplified DNA from CSF cells (14 cases, 14 controls) and blood B cells (10 cases, 10 controls) were analyzed in a subset of participants. Multiple droplet digital PCR (ddPCR) runs were performed per sample to assess the cumulative EBV positivity rate. To detect viral RNA as a sign of activation, RNA sequencing was performed in blood CD4-positive, CD8-positive, and CD19-positive cells from 21 patients with MS and 3 controls.

Results: One of the 45 patients with MS and none of the 45 controls were positive for EBV DNA in CSF supernatants (1 mL). CSF cellular DNA was analyzed in 8 independent ddPCRs: EBV DNA was detected at least once in 18 (64%) of the 28 patients with MS and in 15 (54%) of the 28 controls (p = 0.59, Fisher test). The cumulative EBV positivity increased steadily up to 59% in the successive ddPCRs, suggesting that all individuals would have reached EBV positivity in the CSF cells, if more DNA would have been analyzed. The estimated proportion of EBV-positive B cells was >1/10,000 in both the CSF and blood. We did not detect viral RNA, except from endogenous retroviruses, in the blood lymphocyte subpopulations.

Discussion: EBV-DNA is equally detectable in the CSF cells of both patients with MS and controls with ddPCR, and the probabilistic approach indicates that the true positivity rate approaches 100% in EBV-positive individuals. The proportion of EBV-positive B cells seems higher than previously estimated.

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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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