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脑炎型甲病毒、创伤性脑损伤和有机磷神经毒剂暴露的神经学表现。

Neurological manifestations of encephalitic alphaviruses, traumatic brain injuries, and organophosphorus nerve agent exposure.

作者信息

VanderGiessen Morgen, de Jager Caroline, Leighton Julia, Xie Hehuang, Theus Michelle, Johnson Erik, Kehn-Hall Kylene

机构信息

Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA, United States.

Center for Emerging, Zoonotic, and Arthropod-borne Pathogens, Virginia Polytechnic Institute and State University, Blacksburg, VA, United States.

出版信息

Front Neurosci. 2024 Dec 13;18:1514940. doi: 10.3389/fnins.2024.1514940. eCollection 2024.


DOI:10.3389/fnins.2024.1514940
PMID:39734493
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11671522/
Abstract

Encephalitic alphaviruses (EEVs), Traumatic Brain Injuries (TBI), and organophosphorus nerve agents (NAs) are three diverse biological, physical, and chemical injuries that can lead to long-term neurological deficits in humans. EEVs include Venezuelan, eastern, and western equine encephalitis viruses. This review describes the current understanding of neurological pathology during these three conditions, provides a comparative review of case studies vs. animal models, and summarizes current therapeutics. While epidemiological data on clinical and pathological manifestations of these conditions are known in humans, much of our current mechanistic understanding relies upon animal models. Here we review the animal models findings for EEVs, TBIs, and NAs and compare these with what is known from human case studies. Additionally, research on NAs and EEVs is limited due to their classification as high-risk pathogens (BSL-3) and/or select agents; therefore, we leverage commonalities with TBI to develop a further understanding of the mechanisms of neurological damage. Furthermore, we discuss overlapping neurological damage mechanisms between TBI, NAs, and EEVs that highlight novel medical countermeasure opportunities. We describe current treatment methods for reducing neurological damage induced by individual conditions and general neuroprotective treatment options. Finally, we discuss perspectives on the future of neuroprotective drug development against long-term neurological sequelae of EEVs, TBIs, and NAs.

摘要

脑炎型甲病毒(EEVs)、创伤性脑损伤(TBI)和有机磷神经毒剂(NAs)是三种不同的生物、物理和化学损伤,可导致人类长期神经功能缺损。EEVs包括委内瑞拉马脑炎病毒、东方马脑炎病毒和西方马脑炎病毒。本综述描述了目前对这三种情况下神经病理学的认识,对病例研究与动物模型进行了比较综述,并总结了当前的治疗方法。虽然这些情况在人类中的临床和病理表现的流行病学数据是已知的,但我们目前的许多机制性认识依赖于动物模型。在这里,我们回顾了EEVs、TBIs和NAs的动物模型研究结果,并将其与人类病例研究的已知情况进行比较。此外,由于NAs和EEVs被归类为高风险病原体(生物安全3级)和/或选择制剂,对它们的研究受到限制;因此,我们利用与TBI的共性来进一步了解神经损伤的机制。此外,我们还讨论了TBI、NAs和EEVs之间重叠的神经损伤机制,这些机制突出了新的医学对策机会。我们描述了目前减少个体情况引起的神经损伤的治疗方法和一般的神经保护治疗选择。最后,我们讨论了针对EEVs、TBIs和NAs的长期神经后遗症的神经保护药物开发的未来前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11af/11671522/263d766c76b5/fnins-18-1514940-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11af/11671522/9655b76442e0/fnins-18-1514940-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11af/11671522/aa53c4bff306/fnins-18-1514940-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11af/11671522/263d766c76b5/fnins-18-1514940-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11af/11671522/9655b76442e0/fnins-18-1514940-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11af/11671522/aa53c4bff306/fnins-18-1514940-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11af/11671522/263d766c76b5/fnins-18-1514940-g0003.jpg

相似文献

[1]
Neurological manifestations of encephalitic alphaviruses, traumatic brain injuries, and organophosphorus nerve agent exposure.

Front Neurosci. 2024-12-13

[2]
Neurological Sequelae Resulting from Encephalitic Alphavirus Infection.

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[3]
Comparative pathology study of Venezuelan, eastern, and western equine encephalitis viruses in non-human primates.

Antiviral Res. 2020-10

[4]
Neuropathogenesis of Encephalitic Alphaviruses in Non-Human Primate and Mouse Models of Infection.

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[5]
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[6]
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[7]
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[8]
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Viruses. 2023-1-28

[9]
Encephalitic Alphaviruses Exploit Caveola-Mediated Transcytosis at the Blood-Brain Barrier for Central Nervous System Entry.

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[10]
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引用本文的文献

[1]
Machine learning identifies genes linked to neurological disorders induced by equine encephalitis viruses, traumatic brain injuries, and organophosphorus nerve agents.

Front Comput Neurosci. 2025-5-13

本文引用的文献

[1]
Retrospective Analysis of Blood Biomarkers of Neurological Injury in Human Cases of Viral Infection and Bacterial Sepsis.

J Infect Dis. 2025-3-17

[2]
Molecular Epidemiology of Western Equine Encephalitis Virus, South America, 2023-2024.

Emerg Infect Dis. 2024-9

[3]
Astrocytes, reactive astrogliosis, and glial scar formation in traumatic brain injury.

Neural Regen Res. 2025-4-1

[4]
Characterization of Humanized Mouse Model of Organophosphate Poisoning and Detection of Countermeasures via MALDI-MSI.

Int J Mol Sci. 2024-5-22

[5]
Arbovirus infection increases the risk for the development of neurodegenerative disease pathology in the murine model.

Brain Behav Immun Health. 2024-4-24

[6]
Pesticides impacts on human health and the environment with their mechanisms of action and possible countermeasures.

Heliyon. 2024-4-4

[7]
Sleep, inflammation, and hemodynamics in rodent models of traumatic brain injury.

Front Neurosci. 2024-2-15

[8]
Is Alzheimer disease a disease?

Nat Rev Neurol. 2024-4

[9]
Post-exposure intranasal IFNα suppresses replication and neuroinvasion of Venezuelan Equine Encephalitis virus within olfactory sensory neurons.

J Neuroinflammation. 2024-1-17

[10]
Traumatic brain injury extending to the striatum alters autonomic thermoregulation and hypothalamic monoamines in recovering rats.

Front Neurosci. 2023-12-7

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