IL-15-dependent immune crosstalk between natural killer cells and dendritic cells in HIV-1 elite controllers

被引:3
|
作者
Hartana, Ciputra Adijaya [1 ]
Lancien, Melanie [1 ]
Gao, Ce [1 ]
Rassadkina, Yelizaveta [1 ]
Lichterfeld, Mathias [1 ,2 ,3 ]
Yu, Xu G. [1 ,2 ]
机构
[1] Ragon Inst MGH MIT & Harvard, Cambridge, MA 02139 USA
[2] Brigham & Womens Hosp, Infect Dis Div, Boston, MA 02115 USA
[3] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
来源
CELL REPORTS | 2023年 / 42卷 / 12期
关键词
RNA-SEQ DATA; NK CELL; REPLICATION; ACTIVATION; INDUCTION; INFECTION; MEMORY;
D O I
10.1016/j.celrep.2023.113530
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As the principal effector cell population of the innate immune system, natural killer (NK) cells may make crit-ical contributions to natural, immune-mediated control of HIV-1 replication. Using genome-wide assess-ments of activating and inhibitory chromatin features, we demonstrate here that cytotoxic NK (cNK) cells from elite controllers (ECs) display elevated activating histone modifications at the interleukin 2 (IL-2)/IL-15 receptor b chain and the BCL2 gene loci. These histone changes translate into increased responsiveness of cNK cells to paracrine IL-15 secretion, which coincides with higher levels of IL-15 transcription by myeloid dendritic cells in ECs. The distinct immune crosstalk between these innate immune cell populations results in improved IL-15-dependent cNK cell survival and cytotoxicity, paired with a metabolic profile biased toward IL-15-mediated glycolytic activities. Together, these results suggest that cNK cells from ECs display a pro-grammed IL-15 response signature and support the emerging role of innate immune pathways in natural,-free control of HIV-1.
引用
收藏
页数:18
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