Centre d'Étude des Pathologies Respiratoires (CEPR), Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche 1100, Faculté de Médecine, Université de Tours, Tours, France.
Department of Immunology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Trends Immunol. 2022 Jul;43(7):503-512. doi: 10.1016/j.it.2022.04.012. Epub 2022 May 31.
Invariant natural killer T (iNKT) cells are increasingly regarded as disease biomarkers and immunotherapeutic targets. However, a greater understanding of their biology is necessary to effectively target these cells in the clinic. The discovery of iNKT1/2/17 cell effector subsets was a milestone in our understanding of iNKT cell development and function. Recent transcriptomic studies have uncovered an even greater heterogeneity and challenge our understanding of iNKT cell ontogeny and effector differentiation. We propose a refined model whereby iNKT cells differentiate through a dynamic and continuous instructive process that requires the accumulation and integration of various signals within the thymus or peripheral tissues. Within this framework, we question the existence of true iNKT2 cells and discuss the parallels between mouse and human iNKT cells.
不变自然杀伤 T(iNKT) 细胞越来越被视为疾病生物标志物和免疫治疗靶点。然而,为了在临床上有效地靶向这些细胞,我们需要更深入地了解它们的生物学特性。iNKT1/2/17 细胞效应子亚群的发现是我们理解 iNKT 细胞发育和功能的一个里程碑。最近的转录组学研究揭示了更高的异质性,挑战了我们对 iNKT 细胞发生和效应分化的理解。我们提出了一个经过改进的模型,即 iNKT 细胞通过一个动态和连续的指令性过程进行分化,该过程需要在胸腺或外周组织中积累和整合各种信号。在这个框架内,我们质疑真正的 iNKT2 细胞的存在,并讨论了小鼠和人类 iNKT 细胞之间的相似之处。