| Literature DB >> 26256793 |
Greg M Delgoffe1, Jonathan D Powell2.
Abstract
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.Entities:
Keywords: Anergy; Exhaustion; Metabolism; T cells; Tolerance; mTOR
Mesh:
Year: 2015 PMID: 26256793 PMCID: PMC4837657 DOI: 10.1016/j.molimm.2015.07.026
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407