Delgoffe Greg M, Powell Jonathan D
Tumor Microenvironment Center, Department of Immunology, University of Pittsburgh Cancer Institute, Pittsburgh, PA 15232, United States.
Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21223, United States.
Mol Immunol. 2015 Dec;68(2 Pt C):492-6. doi: 10.1016/j.molimm.2015.07.026.
Through the direct control of infection or by providing cytokine signals to other cellular players, T cells play a central role in the orchestration of the immune response. However, in many disease states, T cells are rendered dysfunctional, unable to carry out their effector functions. As T cell activation is bioenergetically demanding, some T cell dysfunction can have metabolic underpinnings. In this review, we will discuss how T cells are programmed to fuel their effector response, and how programmed or pathologic changes can disrupt their ability to generate the energy needed to proliferate and carry out their critical functions.
通过直接控制感染或向其他细胞参与者提供细胞因子信号,T细胞在协调免疫反应中发挥核心作用。然而,在许多疾病状态下,T细胞会功能失调,无法执行其效应功能。由于T细胞活化对生物能量需求很高,一些T细胞功能障碍可能有代谢基础。在本综述中,我们将讨论T细胞如何被编程以支持其效应反应,以及程序性或病理性变化如何破坏它们产生增殖和执行关键功能所需能量的能力。