Bennstein Sabrina Bianca
Nuffield Department of Surgical Sciences, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.
Front Immunol. 2018 Jan 9;8:1950. doi: 10.3389/fimmu.2017.01950. eCollection 2017.
Natural killer T-cells are a subset of innate-like T-cells with the ability to bridge innate and adaptive immunity. There is great interest in harnessing these cells to improve tumor therapy; however, greater understanding of invariant NKT (iNKT) cell biology is needed. The first step is to learn more about NKT development within the thymus. Recent studies suggest lineage separation of murine iNKT cells into iNKT1, iNKT2, and iNKT17 cells instead of shared developmental stages. This review will focus on these new studies and will discuss the evidence for lineage separation in contrast to shared developmental stages. The author will also highlight the classifications of murine iNKT cells according to identified transcription factors and cytokine production, and will discuss transcriptional and posttranscriptional regulations, and the role of mammalian target of rapamycin. Finally, the importance of these findings for human cancer therapy will be briefly discussed.
自然杀伤T细胞是一类具有连接天然免疫和适应性免疫能力的固有样T细胞亚群。利用这些细胞改善肿瘤治疗引起了人们极大的兴趣;然而,我们需要更深入地了解不变自然杀伤T(iNKT)细胞生物学。第一步是更多地了解胸腺内自然杀伤T细胞的发育。最近的研究表明,小鼠iNKT细胞谱系可分为iNKT1、iNKT2和iNKT17细胞,而不是共享发育阶段。本综述将聚焦于这些新研究,并讨论与共享发育阶段相对的谱系分离证据。作者还将根据已确定的转录因子和细胞因子产生情况强调小鼠iNKT细胞的分类,并讨论转录和转录后调控以及雷帕霉素哺乳动物靶点的作用。最后,将简要讨论这些发现对人类癌症治疗的重要性。