转录组
CD8型
免疫系统
生物
免疫学
T细胞
细胞毒性T细胞
细胞
免疫衰老
基因表达
基因
遗传学
体外
标识
DOI:10.1016/j.it.2023.05.005
摘要
The ability of T cells to undergo robust cell division in response to antigenic stimulation is essential for competent T cell function. However, this ability is reduced with aging and contributes to increased susceptibility to infectious diseases, cancers, and other diseases among older adults. To better understand T cell aging, improved measurements of age-related cellular changes in T cells are necessary. The recent development of machine learning (ML)-assisted transcriptome-based quantification of individual CD8+ T cell age represents a significant step forward in this regard. It reveals both prominent and subtle changes in gene expression and points to potential functional alterations of CD8+ T cells with aging. I argue that single-cell transcriptome-based age prediction in the immune system may have promising future applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI