Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065; and.
Graduate Program in Immunology and Microbial Pathogenesis, Weill Cornell Graduate School of Medical Sciences, Cornell University, New York, NY 10065.
J Immunol. 2018 Jan 15;200(2):408-414. doi: 10.4049/jimmunol.1701124.
Innate lymphoid cells (ILCs) are critical components of tissues in the body, providing a first line of defense against challenges to host integrity. In contrast to strictly cytokine-producing helper ILCs, resident innate lymphocyte populations with cytolytic potential have been identified in multiple tissues in both mouse and human. These cells express the transcription factor Tbet, NK cell receptors, granzymes, perforin, and death receptors, and can directly kill tumor cells. Signals in the tumor microenvironment may promote this response, including the cytokine IL-15 and stress-associated ligands for activating NK receptors. Although there is evidence that these cells are tissue and tumor resident, their lineage remains unclear. Whether they are derived from the NK or helper ILC lineages or represent a third differentiation pathway remains to be determined. A better understanding of their lineage will help clarify their regulation and function in the context of antitumor immunity.
先天淋巴细胞 (ILC) 是体内组织的重要组成部分,为宿主完整性受到挑战提供了第一道防线。与严格的细胞因子产生辅助性 ILC 不同,在小鼠和人类的多种组织中已经鉴定出具有细胞毒性潜力的常驻先天淋巴细胞群体。这些细胞表达转录因子 Tbet、NK 细胞受体、颗粒酶、穿孔素和死亡受体,并可以直接杀死肿瘤细胞。肿瘤微环境中的信号可能会促进这种反应,包括细胞因子 IL-15 和激活 NK 受体的应激相关配体。尽管有证据表明这些细胞是组织和肿瘤驻留的,但它们的谱系仍不清楚。它们是来自 NK 细胞还是辅助性 ILC 谱系,或者代表第三种分化途径,还有待确定。更好地了解它们的谱系将有助于阐明它们在抗肿瘤免疫中的调节和功能。