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自然杀伤细胞在小鼠巨细胞病毒和淋巴细胞性脉络丛脑膜炎病毒感染背景下的多方面作用

The Multifaceted Roles of NK Cells in the Context of Murine Cytomegalovirus and Lymphocytic Choriomeningitis Virus Infections.

作者信息

Hamdan Thamer A

机构信息

Department of Basic Dental Sciences, Faculty of Dentistry, Al-Ahliyya Amman University, Amman 19328, Jordan.

Department of Medical Laboratory Sciences, Faculty of Allied Medical Sciences, Al-Ahliyya Amman University, Amman 19328, Jordan.

出版信息

Immune Netw. 2024 Jun 27;24(4):e29. doi: 10.4110/in.2024.24.e29. eCollection 2024 Aug.

Abstract

NK cells belong to innate lymphoid cells and able to eliminate infected cells and tumor cells. NK cells play a valuable role in controlling viral infections. Also, they have the potential to shape the adaptive immunity via a unique crosstalk with the different immune cells. Murine models are important tools for delineating the immunological phenomena in viral infection. To decipher the immunological virus-host interactions, two major infection models are being investigated in mice regarding NK cell-mediated recognition: murine cytomegalovirus (MCMV) and lymphocytic choriomeningitis virus (LCMV). In this review, we recapitulate recent findings regarding the multifaceted role of NK cells in controlling LCMV and MCMV infections and outline the exquisite interplay between NK cells and other immune cells in these two settings. Considering that, infections with MCMV and LCMV recapitulates many physiopathological characteristics of human cytomegalovirus infection and chronic virus infections respectively, this study will extend our understanding of NK cells biology in interactions between the virus and its natural host.

摘要

自然杀伤细胞属于固有淋巴细胞,能够清除被感染细胞和肿瘤细胞。自然杀伤细胞在控制病毒感染中发挥着重要作用。此外,它们还具有通过与不同免疫细胞的独特相互作用来塑造适应性免疫的潜力。小鼠模型是阐明病毒感染中免疫现象的重要工具。为了解析免疫性病毒-宿主相互作用,目前正在小鼠中研究两种主要的感染模型,以探讨自然杀伤细胞介导的识别作用:小鼠巨细胞病毒(MCMV)和淋巴细胞性脉络丛脑膜炎病毒(LCMV)。在这篇综述中,我们总结了关于自然杀伤细胞在控制LCMV和MCMV感染中的多方面作用的最新发现,并概述了在这两种情况下自然杀伤细胞与其他免疫细胞之间的精妙相互作用。鉴于MCMV和LCMV感染分别概括了人类巨细胞病毒感染和慢性病毒感染的许多生理病理特征,本研究将扩展我们对病毒与其天然宿主相互作用中自然杀伤细胞生物学的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322c/11377952/b2beb3265fc1/in-24-e29-g001.jpg

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