Carayannopoulos Leonidas N, Yokoyama Wayne M
Howard Hughes Medical Institute, Division of Pulmonary and Critical Care Medicine, Washington University Medical Center, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Curr Opin Immunol. 2004 Feb;16(1):26-33. doi: 10.1016/j.coi.2003.11.003.
Under the influence of cytokines associated with innate immunity, natural killer (NK) cells rapidly become activated and migrate to sites of infection. Upon contact with infected parenchyma they proliferate, release cytokines and/or kill cells harboring pathogens. Multiple stimulatory and inhibitory receptors can provide the integrated signals that trigger this contact-mediated NK-cell function. Recent work has begun to define the ligands for these receptors in the context of infection by certain well-studied viruses. These results, in addition to future work involving other pathogens, will provide an understanding of the molecules present on parasitized cells that mark them as targets of innate immunity.
在与先天免疫相关的细胞因子影响下,自然杀伤(NK)细胞迅速被激活并迁移至感染部位。与受感染的实质细胞接触后,它们会增殖、释放细胞因子和/或杀死携带病原体的细胞。多种刺激和抑制性受体可提供触发这种接触介导的NK细胞功能的整合信号。最近的研究已开始在某些经过充分研究的病毒感染背景下确定这些受体的配体。这些结果以及未来涉及其他病原体的研究,将有助于理解被寄生细胞上存在的、将它们标记为先天免疫靶点的分子。