Laboratory of Infectious Diseases and Vaccines, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, PR China.
ImmunoTechnology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, 20892, USA.
Immunol Cell Biol. 2019 Jul;97(6):586-596. doi: 10.1111/imcb.12248. Epub 2019 Apr 8.
The peripheral maturation of human CD1d-restricted natural killer T (NKT) cells has not been well described. In this study, we identified four major subsets of NKT cells in adults, distinguished by the expression of CD4, CD8 and CCR5. Phenotypic analysis suggested a hierarchical pattern of differentiation, whereby immature CD4 CD8 CCR5 cells progressed to an intermediate CD4 CD8 CCR5 stage, which remained less differentiated than the CD4 CD8 and CD4 CD8 subsets, both of which expressed CCR5. This interpretation was supported by functional data, including clonogenic potential and cytokine secretion profiles, as well as T-cell receptor (TCR) excision circle analysis. Moreover, conventional and high-throughput sequencing of the corresponding TCR repertoires demonstrated significant clonotypic overlap within individuals, especially between the more differentiated CD4 CD8 and CD4 CD8 subsets. Collectively, these results mapped a linear differentiation pathway across the post-thymic landscape of human CD1d-restricted NKT cells.
人类 CD1d 限制性自然杀伤 T(NKT)细胞的外周成熟尚未得到很好的描述。在这项研究中,我们在成人中鉴定了 NKT 细胞的四个主要亚群,通过表达 CD4、CD8 和 CCR5 来区分。表型分析表明存在一种分化的层次模式,不成熟的 CD4+CD8+CCR5 细胞进展为中间 CD4+CD8+CCR5 阶段,该阶段的分化程度低于 CD4+CD8 和 CD4+CD8 亚群,后两者均表达 CCR5。这一解释得到了功能数据的支持,包括集落形成潜力和细胞因子分泌谱,以及 T 细胞受体(TCR)切除环分析。此外,相应 TCR 库的常规和高通量测序显示个体内存在显著的克隆型重叠,尤其是在分化程度更高的 CD4+CD8 和 CD4+CD8 亚群之间。综上所述,这些结果描绘了人类 CD1d 限制性 NKT 细胞在胸腺后景观中的线性分化途径。