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雪貂感染 H5N1 病毒的神经病理学研究。

Neuropathology of H5N1 virus infection in ferrets.

机构信息

Galveston National Laboratory, Sealy Vaccine Center and Institute for Human Infections and Immunity, Department of Pathology, University of Texas Medical Branch (UTMB), Galveston, TX 77555-0609, USA.

出版信息

Vet Microbiol. 2012 May 4;156(3-4):294-304. doi: 10.1016/j.vetmic.2011.11.025. Epub 2011 Dec 2.

Abstract

Highly pathogenic H5N1 virus remains a potential threat to humans. Over 289 fatalities have been reported in WHO confirmed human cases since 2003, and lack of effective vaccines and early treatments contribute to increasing numbers of cases and fatalities. H5N1 encephalitis is a recognized cause of death in Vietnamese cases, and brain pathology is described in other human cases and naturally infected animals. However, neither pathogenesis of H5N1 viral infection in human brain nor post-infection effects in survivors have been fully investigated. We report the brain pathology in a ferret model for active infection and 18-day survival stages. This model closely resembles the infection pattern and progression in human cases of influenza A, and our report is the first description of brain pathology for longer term (18-day) survival in ferrets. We analyzed viral replication, type and severity of meningoencephalitis, infected cell types, and cellular responses to infection. We found viral replication to very high titers in ferret brain, closely correlating with severity of meningoencephalitis. Viral antigens were detected predominantly in neurons, correlating with inflammatory lesions, and less frequently in astrocytes and ependymal cells during active infection. Mononuclear cell infiltrates were observed in early stages predominantly in cerebral cortex, brainstem, and leptomeninges, and less commonly in cerebellum and other areas. Astrogliosis was mild at day 4 post-infection, but robust by day 18. Early and continuous treatment with an antiviral agent (peramivir) inhibited virus production to non-detectable levels, reduced severity of brain injury, and promoted higher survival rates.

摘要

高致病性 H5N1 病毒仍然是人类的潜在威胁。自 2003 年以来,世界卫生组织确认的人类病例中已有 289 人死亡,缺乏有效的疫苗和早期治疗导致病例和死亡人数不断增加。H5N1 脑炎是越南病例死亡的公认原因,其他人类病例和自然感染动物的脑病理学已有描述。然而,H5N1 病毒感染人类大脑的发病机制以及感染后幸存者的影响尚未得到充分研究。我们报告了在活跃感染和 18 天存活阶段的雪貂模型中的脑病理学。该模型与人感染甲型流感的感染模式和进展非常相似,我们的报告是首次描述在雪貂中存活时间较长(18 天)的脑病理学。我们分析了病毒复制、脑膜脑炎的类型和严重程度、感染的细胞类型以及细胞对感染的反应。我们发现雪貂大脑中的病毒复制达到非常高的滴度,与脑膜脑炎的严重程度密切相关。在活跃感染期间,病毒抗原主要在神经元中检测到,与炎症病变相关,在星形胶质细胞和室管膜细胞中较少检测到。单核细胞浸润在早期主要观察到大脑皮层、脑干和软脑膜,在小脑和其他区域较少观察到。感染后第 4 天星形胶质细胞增生轻微,但第 18 天则很强。早期和连续使用抗病毒药物(帕拉米韦)治疗可抑制病毒产生,使其无法检测到,降低脑损伤严重程度,并提高存活率。

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