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爱泼斯坦-巴尔病毒与多发性硬化症:为开发更好的非人灵长类动物模型所汲取的经验教训。

Epstein-Barr virus and multiple sclerosis: lesson learned to develop better nonhuman primate models.

作者信息

Nguyen Hai Duc, Kim Daesik, Kim Yong-Hee, Flemington Erik, Giovannoni Gavin, Park Chung-Gyu, Kim Woong-Ki

机构信息

Division of Microbiology, Tulane National Primate Research Center, Tulane University, Covington, LA, USA.

Transplantation Research Institute, Seoul National University, Seoul, South Korea.

出版信息

Exp Mol Med. 2025 Jun;57(6):1143-1151. doi: 10.1038/s12276-025-01482-5. Epub 2025 Jun 30.

DOI:10.1038/s12276-025-01482-5
PMID:40588526
Abstract

Multiple sclerosis (MS) is a chronic autoimmune disorder with a complex etiology, and Epstein-Barr virus (EBV) is considered the leading cause. While understanding the role of EBV infection in the pathogenesis of MS in human subjects is crucial, animal models, particularly nonhuman primates (NHPs), would provide an ideal controlled environment for testing EBV hypotheses and identifying potential therapeutic targets. Here in this Review we address clinically relevant questions regarding the link between EBV infection and MS to inform the development and refinement of virally induced NHP models. We focus on integrating known EBV-related risk factors for MS, including age at infection, infectious mononucleosis, genetic predispositions such as the human leukocyte antigen (HLA)-DR15 haplotype, sex-specific susceptibility, low vitamin D levels and CD8 T cell deficiency. We also explore the application of these risk factors in model development, investigate why most EBV-infected individuals do not develop MS and propose potential disease-modifying therapeutic options and vaccines. Integrating these approaches into NHP models will improve our understanding of MS pathogenesis and guide the development of targeted strategies for disease management and prevention. We propose to develop a refined EBV infection NHP model of MS coupled with CD8 cell depletion and other inclusion and exclusion criteria.

摘要

多发性硬化症(MS)是一种病因复杂的慢性自身免疫性疾病,而爱泼斯坦-巴尔病毒(EBV)被认为是主要病因。虽然了解EBV感染在人类MS发病机制中的作用至关重要,但动物模型,特别是非人类灵长类动物(NHP),将为测试EBV假说和确定潜在治疗靶点提供理想的可控环境。在本综述中,我们探讨了与EBV感染和MS之间联系相关的临床问题,以为病毒诱导的NHP模型的开发和完善提供参考。我们着重整合已知的MS相关EBV危险因素,包括感染年龄、传染性单核细胞增多症、遗传易感性(如人类白细胞抗原(HLA)-DR15单倍型)、性别特异性易感性、低维生素D水平和CD8 T细胞缺陷。我们还探讨了这些危险因素在模型开发中的应用,研究为何大多数EBV感染个体不会患MS,并提出潜在的疾病改善治疗选择和疫苗。将这些方法整合到NHP模型中将增进我们对MS发病机制的理解,并指导疾病管理和预防的靶向策略的开发。我们建议开发一种完善的MS的EBV感染NHP模型,结合CD8细胞耗竭以及其他纳入和排除标准。

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Epstein-Barr virus and multiple sclerosis: lesson learned to develop better nonhuman primate models.爱泼斯坦-巴尔病毒与多发性硬化症:为开发更好的非人灵长类动物模型所汲取的经验教训。
Exp Mol Med. 2025 Jun;57(6):1143-1151. doi: 10.1038/s12276-025-01482-5. Epub 2025 Jun 30.
2
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Cochrane Database Syst Rev. 2021 Nov 16;11(11):CD013647. doi: 10.1002/14651858.CD013647.pub2.

本文引用的文献

1
Emboldened or not: The potential fall-out of a failed anti-EBV trial in multiple sclerosis.成败与否:多发性硬化症中一项抗EBV试验失败的潜在后果。
Mult Scler Relat Disord. 2024 Jan;81:105364. doi: 10.1016/j.msard.2023.105364. Epub 2023 Dec 10.
2
Immune control of human γ-herpes infections.人类γ-疱疹病毒感染的免疫控制
Semin Arthritis Rheum. 2024 Feb;64S:152320. doi: 10.1016/j.semarthrit.2023.152320. Epub 2023 Nov 21.
3
Regulation of CD8 T memory and exhaustion by the mTOR signals.mTOR 信号对 CD8 T 细胞记忆和耗竭的调节。
Cell Mol Immunol. 2023 Sep;20(9):1023-1039. doi: 10.1038/s41423-023-01064-3. Epub 2023 Aug 15.
4
Epstein-Barr virus and multiple sclerosis: moving from questions of association to questions of mechanism.爱泼斯坦-巴尔病毒与多发性硬化症:从关联性问题转向机制性问题。
Clin Transl Immunology. 2023 May 17;12(5):e1451. doi: 10.1002/cti2.1451. eCollection 2023.
5
Immunosenescence: molecular mechanisms and diseases.免疫衰老:分子机制与疾病。
Signal Transduct Target Ther. 2023 May 13;8(1):200. doi: 10.1038/s41392-023-01451-2.
6
Epstein-Barr virus as a leading cause of multiple sclerosis: mechanisms and implications.EB 病毒是多发性硬化症的主要病因:机制和意义。
Nat Rev Neurol. 2023 Mar;19(3):160-171. doi: 10.1038/s41582-023-00775-5. Epub 2023 Feb 9.
7
Targeting integrin pathways: mechanisms and advances in therapy.靶向整合素途径:机制与治疗进展。
Signal Transduct Target Ther. 2023 Jan 2;8(1):1. doi: 10.1038/s41392-022-01259-6.
8
What do animal models tell us about the role of EBV in the pathogenesis of multiple sclerosis?动物模型向我们揭示了 EBV 在多发性硬化症发病机制中的作用吗?
Front Immunol. 2022 Nov 17;13:1036155. doi: 10.3389/fimmu.2022.1036155. eCollection 2022.
9
Increased expression of PD-1 in CD8  CD3  T cells correlates with EBV viral load in MS patients.CD8+CD3+T 细胞中 PD-1 的表达增加与 MS 患者 EBV 病毒载量相关。
J Neurovirol. 2022 Dec;28(4-6):497-504. doi: 10.1007/s13365-022-01083-2. Epub 2022 Oct 15.
10
Infectious mononucleosis is associated with an increased incidence of multiple sclerosis: Results from a cohort study of 32,116 outpatients in Germany.传染性单核细胞增多症与多发性硬化症的发病率增加有关:来自德国 32116 名门诊患者队列研究的结果。
Front Immunol. 2022 Aug 2;13:937583. doi: 10.3389/fimmu.2022.937583. eCollection 2022.