Münz Christian, Chijioke Obinna
Viral Immunobiology, Institute of Experimental Immunology, University of Zurich, Winterthurerstrasse, Zurich, Switzerland.
Institute of Pathology and Molecular Pathology, University Hospital Zurich, Schmelzbergstrasse, Zurich, Switzerland.
F1000Res. 2017 Jul 26;6. doi: 10.12688/f1000research.11197.1. eCollection 2017.
Natural killer (NK) cells are potent innate cytotoxic lymphocytes for the destruction of infected and transformed cells. Although they were originally considered to be ready-made assassins after their hematopoietic development, it has recently become clear that their activity is regulated by mechanisms such as repertoire composition, licensing, priming, and adaptive memory-like differentiation. Some of these mechanisms are influenced by infectious disease agents, including herpesviruses. In this review, we will compare expansion, stimulation, and effector functions of NK cell populations after infections with β- and γ -herpesviruses because, though closely related, these pathogens seem to drive completely opposite NK cell responses. The discussed findings suggest that different NK cell subsets expand and perform protective functions during infectious diseases and might be used diagnostically to predict resistance to the causative pathogens as well as treat them by adoptive transfer of the respective populations.
自然杀伤(NK)细胞是一种强大的先天性细胞毒性淋巴细胞,可用于破坏受感染和发生转化的细胞。尽管它们最初在造血发育后被认为是现成的杀手,但最近已经清楚地认识到,它们的活性受诸如库组成、许可、启动和适应性记忆样分化等机制的调节。其中一些机制受到包括疱疹病毒在内的传染病病原体的影响。在这篇综述中,我们将比较感染β-和γ-疱疹病毒后NK细胞群体的扩增、刺激和效应功能,因为尽管这些病原体密切相关,但它们似乎会驱动完全相反的NK细胞反应。所讨论的研究结果表明,不同的NK细胞亚群在传染病期间会扩增并发挥保护功能,并且可能在诊断上用于预测对致病病原体的抵抗力,以及通过相应群体的过继转移来治疗这些病原体。