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与致命性东部马脑炎病毒在猕猴中相关的大脑的生理和免疫变化。

Physiological and immunological changes in the brain associated with lethal eastern equine encephalitis virus in macaques.

机构信息

Center for Vaccine Research, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.

Department of Infectious Diseases and Microbiology, School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.

出版信息

PLoS Pathog. 2021 Feb 3;17(2):e1009308. doi: 10.1371/journal.ppat.1009308. eCollection 2021 Feb.

Abstract

Aerosol exposure to eastern equine encephalitis virus (EEEV) can trigger a lethal viral encephalitis in cynomolgus macaques which resembles severe human disease. Biomarkers indicative of central nervous system (CNS) infection by the virus and lethal outcome of disease would be useful in evaluating potential medical countermeasures, especially for therapeutic compounds. To meet requirements of the Animal Rule, a better understanding of the pathophysiology of EEEV-mediated disease in cynomolgus macaques is needed. In this study, macaques given a lethal dose of clone-derived EEEV strain V105 developed a fever between 2-3 days post infection (dpi) and succumbed to the disease by 6 dpi. At the peak of the febrile phase, there was a significant increase in the delta electroencephalography (EEG) power band associated with deep sleep as well as a sharp rise in intracranial pressure (ICP). Viremia peaked early after infection and was largely absent by the onset of fever. Granulocytosis and elevated plasma levels of IP-10 were found early after infection. At necropsy, there was a one hundred- to one thousand-fold increase in expression of traumatic brain injury genes (LIF, MMP-9) as well as inflammatory cytokines and chemokines (IFN-γ, IP-10, MCP-1, IL-8, IL-6) in the brain tissues. Phenotypic analysis of leukocytes entering the brain identified cells as primarily lymphoid (T, B, NK cells) with lower levels of infiltrating macrophages and activated microglia. Massive amounts of infectious virus were found in the brains of lethally-infected macaques. While no infectious virus was found in surviving macaques, quantitative PCR did find evidence of viral genomes in the brains of several survivors. These data are consistent with an overwhelming viral infection in the CNS coupled with a tremendous inflammatory response to the infection that may contribute to the disease outcome. Physiological monitoring of EEG and ICP represent novel methods for assessing efficacy of vaccines or therapeutics in the cynomolgus macaque model of EEEV encephalitis.

摘要

东方马脑炎病毒(EEEV)气溶胶暴露可在食蟹猴中引发致命的病毒性脑炎,类似于严重的人类疾病。指示病毒对中枢神经系统(CNS)感染和疾病致死结局的生物标志物将有助于评估潜在的医疗对策,特别是治疗性化合物。为了满足动物规则的要求,需要更好地了解 EEEV 在食蟹猴中的发病机制。在这项研究中,给予致死剂量克隆衍生的 EEEV 株 V105 的食蟹猴在感染后 2-3 天(dpi)出现发热,并在 6 dpi 时死于该疾病。在发热期的高峰期,与深度睡眠相关的脑电图(EEG)功率带的 delta 显著增加,颅内压(ICP)急剧上升。病毒血症在感染后早期达到高峰,并在发热开始时基本消失。感染后早期发现粒细胞增多和 IP-10 血浆水平升高。尸检时,脑组织中创伤性脑损伤基因(LIF、MMP-9)以及炎症细胞因子和趋化因子(IFN-γ、IP-10、MCP-1、IL-8、IL-6)的表达增加了 100 到 1000 倍。进入大脑的白细胞的表型分析表明,细胞主要是淋巴细胞(T、B、NK 细胞),浸润的巨噬细胞和激活的小胶质细胞水平较低。在致死性感染的食蟹猴大脑中发现了大量传染性病毒。虽然在幸存的食蟹猴中未发现传染性病毒,但定量 PCR 确实在数名幸存者的大脑中发现了病毒基因组的证据。这些数据与中枢神经系统中压倒性的病毒感染以及对感染的巨大炎症反应一致,这可能导致疾病结局。EEG 和 ICP 的生理监测代表了评估 EEEV 脑炎食蟹猴模型中疫苗或治疗剂疗效的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9453/7886169/c6195458e9bc/ppat.1009308.g001.jpg

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