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先天免疫对抗 Orthohantaviruses:不同的免疫相互作用能否解释宿主特异性疾病结局?

Innate Immunity to Orthohantaviruses: Could Divergent Immune Interactions Explain Host-specific Disease Outcomes?

机构信息

Department of Molecular Genetics and Microbiology, University of New Mexico, 915 Camino de Salud, Albuquerque, NM 87131, United States.

出版信息

J Mol Biol. 2022 Mar 30;434(6):167230. doi: 10.1016/j.jmb.2021.167230. Epub 2021 Sep 4.

DOI:10.1016/j.jmb.2021.167230
PMID:34487792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8894506/
Abstract

The genus Orthohantavirus (family Hantaviridae, order Bunyavirales) consists of numerous genetic and pathologically distinct viral species found within rodent and mammalian insectivore populations world-wide. Although reservoir hosts experience persistent asymptomatic infection, numerous rodent-borne orthohantaviruses cause severe disease when transmitted to humans, with case-fatality rates up to 40%. The first isolation of an orthohantavirus occurred in 1976 and, since then, the field has made significant progress in understanding the immune correlates of disease, viral interactions with the human innate immune response, and the immune kinetics of reservoir hosts. Much still remains elusive regarding the molecular mechanisms of orthohantavirus recognition by the innate immune response and viral antagonism within the reservoir host, however. This review provides a summary of the last 45 years of research into orthohantavirus interaction with the host innate immune response. This summary includes discussion of current knowledge involving human, non-reservoir rodent, and reservoir innate immune responses to viruses which cause hemorrhagic fever with renal syndrome and hantavirus cardio-pulmonary syndrome. Review of the literature concludes with a brief proposition for the development of novel tools needed to drive forward investigations into the molecular mechanisms of innate immune activation and consequences for disease outcomes in the various hosts for orthohantaviruses.

摘要

正汉坦病毒属(汉坦病毒科,布尼亚病毒目)由许多在全世界啮齿动物和哺乳动物食虫动物种群中发现的具有不同遗传和病理特征的病毒种组成。尽管储存宿主经历持续的无症状感染,但当许多啮齿动物传播的正汉坦病毒传播给人类时,会导致严重疾病,病死率高达 40%。第一个正汉坦病毒的分离发生在 1976 年,自那时以来,该领域在理解疾病的免疫相关性、病毒与人类先天免疫反应的相互作用以及储存宿主的免疫动力学方面取得了重大进展。然而,关于先天免疫反应对正汉坦病毒的识别以及储存宿主内病毒拮抗的分子机制,仍有许多未知之处。这篇综述提供了过去 45 年对正汉坦病毒与宿主先天免疫反应相互作用的研究总结。该综述包括对涉及引起肾综合征出血热和汉坦病毒心肺综合征的人类、非储存宿主啮齿动物和储存宿主先天免疫反应的现有知识的讨论。文献综述以对开发新型工具的简要建议结束,这些工具需要推动对先天免疫激活的分子机制以及各种正汉坦病毒宿主的疾病结果的研究。

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Genetic depletion studies inform receptor usage by virulent hantaviruses in human endothelial cells.遗传缺失研究阐明了强毒汉坦病毒在人血管内皮细胞中的受体利用情况。
Elife. 2021 Jul 6;10:e69708. doi: 10.7554/eLife.69708.
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Establishment of a Reverse Genetic System of Severe Fever with Thrombocytopenia Syndrome Virus Based on a C4 Strain.基于C4株的严重发热伴血小板减少综合征病毒反向遗传系统的建立
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Differential pathogenesis between Andes virus strains CHI-7913 and Chile-9717869in Syrian Hamsters.
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Orthohantavirus Replication in the Context of Innate Immunity.Orthohantavirus 复制与固有免疫的关系
Viruses. 2023 May 9;15(5):1130. doi: 10.3390/v15051130.
5
IL-15 induced bystander activation of CD8 T cells may mediate endothelium injury through NKG2D in Hantaan virus infection.汉坦病毒感染中,IL-15 诱导的 CD8 T 细胞旁观者激活可能通过 NKG2D 介导内皮细胞损伤。
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安第斯病毒毒株CHI-7913和智利-9717869在叙利亚仓鼠中的致病机制差异
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Interactions of Viral Proteins from Pathogenic and Low or Non-Pathogenic Orthohantaviruses with Human Type I Interferon Signaling.致病性和低致病性或非致病性正粘病毒的病毒蛋白与人 I 型干扰素信号转导的相互作用。
Viruses. 2021 Jan 19;13(1):140. doi: 10.3390/v13010140.
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