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病毒 CD229(Ly9)同源物作为宿主免疫的新调节剂。

Viral CD229 (Ly9) homologs as new manipulators of host immunity.

机构信息

Immunology Unit, Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.

Institut d'Investigacions Biomèdiques, August Pi i Sunyer, Barcelona, Spain.

出版信息

J Leukoc Biol. 2019 May;105(5):947-954. doi: 10.1002/JLB.2MR1018-413R. Epub 2019 Feb 21.

DOI:10.1002/JLB.2MR1018-413R
PMID:30791129
Abstract

The signaling lymphocytic activation molecule family (SLAMF) of receptors plays crucial roles during innate and adaptive immune responses. The SLAMF member CD229 (Ly9, SLAMF3) is a homophilic receptor predominantly expressed on the surface of B and T cells. CD229 acts as a cosignaling molecule, regulating lymphocyte homoeostasis and activation. To promote viral replication and survival in their hosts, viruses have developed sophisticated mechanisms to combat and avoid immune surveillance. Many of these strategies rely on host defense genes captured during the process of virus-host coevolution. In particular, large DNA viruses devote a wide range of proteins to interfere with almost every host immune pathway. Given that CD229 is critically involved in regulating immune responses, it is not surprising that viruses have designed tactics to mimic or interfere with this receptor. The discovery, in recent years, that some viruses have hijacked CD229 genes from their hosts, incorporating them as an integral part of their genomes, or have evolved proteins to directly target CD229, indicates that this is the case. While it is still an emerging area of research, the present review discusses these viral molecules and their potential in immune modulation. A more detailed understanding of the mechanisms of action and the functional implications of these new viral CD229 mimics may not only provide seminal information on viral immune evasion mechanisms but also, unveil unrecognized aspects of CD229 immune functions.

摘要

信号淋巴细胞激活分子家族(SLAMF)受体在先天和适应性免疫反应中发挥着关键作用。SLAMF 成员 CD229(Ly9,SLAMF3)是一种主要表达于 B 和 T 细胞表面的同型受体。CD229 作为共信号分子,调节淋巴细胞的同源性和激活。为了促进其在宿主中的复制和存活,病毒已经开发出复杂的机制来对抗和避免免疫监视。这些策略中的许多依赖于病毒-宿主共同进化过程中捕获的宿主防御基因。特别是,大型 DNA 病毒专门投入了大量的蛋白质来干扰几乎每一种宿主免疫途径。鉴于 CD229 在调节免疫反应中起着至关重要的作用,病毒设计策略来模拟或干扰这种受体也就不足为奇了。近年来的发现表明,一些病毒从宿主中劫持了 CD229 基因,将其整合到基因组中作为其固有部分,或者进化出蛋白质直接靶向 CD229,这表明确实如此。虽然这仍然是一个新兴的研究领域,但本综述讨论了这些病毒分子及其在免疫调节中的潜力。对这些新的病毒 CD229 模拟物的作用机制和功能意义的更详细了解,不仅可能提供关于病毒免疫逃避机制的重要信息,而且还可能揭示 CD229 免疫功能的未被认识的方面。

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