Meza Guzman Lizeth G, Keating Narelle, Nicholson Sandra E
The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia.
Department of Medical Biology, The University of Melbourne, Parkville, VIC 3010, Australia.
Cancers (Basel). 2020 Apr 11;12(4):952. doi: 10.3390/cancers12040952.
Natural killer (NK) cells play a pivotal role in cancer immunotherapy due to their innate ability to detect and kill tumorigenic cells. The decision to kill is determined by the expression of a myriad of activating and inhibitory receptors on the NK cell surface. Cell-to-cell engagement results in either self-tolerance or a cytotoxic response, governed by a fine balance between the signaling cascades downstream of the activating and inhibitory receptors. To evade a cytotoxic immune response, tumor cells can modulate the surface expression of receptor ligands and additionally, alter the conditions in the tumor microenvironment (TME), tilting the scales toward a suppressed cytotoxic NK response. To fully harness the killing power of NK cells for clinical benefit, we need to understand what defines the threshold for activation and what is required to break tolerance. This review will focus on the intracellular signaling pathways activated or suppressed in NK cells and the roles signaling intermediates play during an NK cytotoxic response.
自然杀伤(NK)细胞因其天生具备检测和杀伤致瘤细胞的能力,在癌症免疫治疗中发挥着关键作用。杀伤的决定由NK细胞表面众多激活和抑制受体的表达来决定。细胞间的相互作用导致自我耐受或细胞毒性反应,这由激活和抑制受体下游信号级联之间的精细平衡所控制。为了逃避细胞毒性免疫反应,肿瘤细胞可以调节受体配体的表面表达,此外,还可以改变肿瘤微环境(TME)中的条件,使天平向抑制细胞毒性NK反应倾斜。为了充分利用NK细胞的杀伤能力以获得临床益处,我们需要了解激活阈值的定义以及打破耐受所需的条件。本综述将聚焦于NK细胞中被激活或抑制的细胞内信号通路,以及信号中间体在NK细胞毒性反应中所起的作用。