Vail Krystal J, Macha Brittany N, Hellmers Linh, Fischer Tracy
Division of Comparative Pathology, Tulane National Primate Research Center, Covington, LA 70433, USA.
Int J Mol Sci. 2025 Jul 17;26(14):6886. doi: 10.3390/ijms26146886.
While viral pathogens are often subdivided into neurotropic and non-neurotropic categories, systemic inflammation caused by non-neurotropic viruses still possesses the ability to alter the central nervous system (CNS). Studies of CNS disease induced by viral infection, whether neurotropic or not, are presented with a unique set of challenges. First, because brain biopsies are rarely necessary to diagnose viral-associated neurological disorders, antemortem tissue samples are not readily available for study and human pathological studies must rely on end-stage, postmortem evaluations. Second, in vitro models fail to fully capture the nuances of an intact immune system, necessitating the use of animal models to fully characterize pathogenesis and identify potential therapeutic approaches. Non-human primates (NHP) represent a particularly attractive animal model in that they overcome many of the limits posed by more distant species and most closely mirror human disease pathogenesis and susceptibility. Here, we review NHP infection models of viruses known to infect and/or replicate within cells of the CNS, including West Nile virus, the equine encephalitis viruses, Zika virus, and herpesviruses, as well as those known to alter the immune status of the brain in the absence of significant CNS penetrance, including human immunodeficiency virus (HIV) in the current era of combination antiretroviral therapy (cART) and the coronavirus of severe acute respiratory syndrome (SARS)-CoV-2. This review focuses on viruses with an established role in causing CNS disease, including encephalitis, meningitis, and myelitis and NHP models of viral infection that are directly translatable to the human condition through relevant routes of infection, comparable disease pathogenesis, and responses to therapeutic intervention.
虽然病毒病原体通常可分为嗜神经病毒和非嗜神经病毒两类,但非嗜神经病毒引起的全身炎症仍具有改变中枢神经系统(CNS)的能力。对病毒感染引起的中枢神经系统疾病的研究,无论病毒是否嗜神经,都面临着一系列独特的挑战。首先,由于诊断病毒相关神经系统疾病很少需要进行脑活检,生前组织样本难以获取用于研究,人类病理学研究必须依赖终末期的尸检评估。其次,体外模型无法完全捕捉完整免疫系统的细微差别,因此需要使用动物模型来全面表征发病机制并确定潜在的治疗方法。非人灵长类动物(NHP)是一种特别有吸引力的动物模型,因为它们克服了许多更远缘物种所带来的限制,并且最能反映人类疾病的发病机制和易感性。在这里,我们综述了已知感染和/或在中枢神经系统细胞内复制的病毒的非人灵长类动物感染模型,包括西尼罗河病毒、马脑炎病毒、寨卡病毒和疱疹病毒,以及那些已知在没有明显中枢神经系统侵袭的情况下改变脑部免疫状态的病毒,包括在当前联合抗逆转录病毒疗法(cART)时代的人类免疫缺陷病毒(HIV)和严重急性呼吸综合征冠状病毒(SARS)-CoV-2。本综述重点关注在引起中枢神经系统疾病(包括脑炎、脑膜炎和脊髓炎)中起既定作用的病毒,以及通过相关感染途径、可比的疾病发病机制和对治疗干预的反应可直接转化为人类情况的病毒感染的非人灵长类动物模型。