Nguyen Hai Duc, Kim Daesik, Kim Yong-Hee, Flemington Erik, Giovannoni Gavin, Park Chung-Gyu, Kim Woong-Ki
Division of Microbiology, Tulane National Primate Research Center, Tulane University, Covington, LA, USA.
Transplantation Research Institute, Seoul National University, Seoul, South Korea.
Exp Mol Med. 2025 Jun;57(6):1143-1151. doi: 10.1038/s12276-025-01482-5. Epub 2025 Jun 30.
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.
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。