Running to Stand Still: Naive CD8+ T Cells Actively Maintain a Program of Quiescence

CD8(+) T cells play a pivotal role in clearing intracellular pathogens and combatting tumours. Upon infection, naive CD8(+) T cells differentiate into effector and memory cells, and this program is underscored by large-scale and coordinated changes in the chromatin architecture and gene expression. Importantly, recent evidence demonstrates that the epigenetic mechanisms that regulate the capacity for rapid effector function of memory T cells are shared by innate immune cells such as natural killer (NK) cells. Thus, it appears that the crucial difference between innate and adaptive immunity is the presence of the naive state. This important distinction raises an intriguing new hypothesis, that the naive state was evolutionary installed to restrain a default program of effector and memory differentiation in response to antigen recognition. We argue that the hallmark of adaptive T immunity is therefore the naive program, which actively maintains CD8(+) T cell quiescence until receipt of appropriate activation signals. In this review, we examine the mechanistic control of naive CD8(+) T cell quiescence and summarise the multiple levels of restraint imposed in naive cells in to limit spontaneous and inappropriate activation. This includes epigenetic mechanisms and transcription factor (TF) regulation of gene expression, in addition to novel inhibitory receptors, abundance of RNA, and protein degradation.