Bone Marrow Transplant and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee 38105-3678, USA.
Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Cold Spring Harb Perspect Biol. 2022 Mar 1;14(3):a037804. doi: 10.1101/cshperspect.a037804.
The pool of memory CD8 T cells is comprised of highly specialized subpopulations of cells with both shared and distinct functions. The ongoing study of T-cell memory is focused on how these different subpopulations arise, how the cells are maintained over the life of the host, and how the cells protect a host against reinfection. As a field we have used the convenience of a narrow range of surface markers to define and study these memory T-cell subsets. However, as we learn more about these cells, it is becoming clear that these broad definitions are insufficient to capture the complexity of the CD8 memory T-cell pool, and an updated definition of these cellular states are needed. Here, we discuss data that have recently arisen that highlight the difficulty in using surface markers to functionally characterize CD8 T-cell populations, and the possibility of using the epigenetic state of cells to more clearly define the functional capacity of CD8 memory T-cell subsets.
记忆 CD8 T 细胞库由具有共享和独特功能的高度专业化细胞亚群组成。目前对 T 细胞记忆的研究集中在这些不同亚群如何产生、细胞如何在宿主的一生中维持以及细胞如何保护宿主免受再感染。作为一个领域,我们已经利用一系列狭窄的表面标记物来定义和研究这些记忆 T 细胞亚群的便利性。然而,随着我们对这些细胞了解的增多,很明显,这些广泛的定义不足以捕捉 CD8 记忆 T 细胞库的复杂性,因此需要对这些细胞状态进行更新定义。在这里,我们讨论了最近出现的数据,这些数据突出了使用表面标记物来对 CD8 T 细胞群体进行功能特征描述的困难,以及使用细胞的表观遗传状态更清楚地定义 CD8 记忆 T 细胞亚群的功能能力的可能性。