Targeting T cell metabolism to regulate T cell activation, differentiation and function in disease

Curr Opin Immunol. 2017 Jun:46:82-88. doi: 10.1016/j.coi.2017.04.006. Epub 2017 May 15.

Abstract

It is becoming increasingly clear that metabolic reprogramming plays a critical role in T cell activation, differentiation and function. To this end, cellular metabolism not only meets the energetic demands of T cells but also provides critical substrates for their growth and function. Furthermore, metabolites themselves are emerging as key regulators of immune responses. As the details of how metabolic reprogramming regulates immune function are revealed, new potential targets for modulating immune responses have emerged. Indeed, the distinct metabolic demands of different T cell subsets make them exquisitely sensitive to pharmacologic inhibitors of metabolism. In this review, we will describe the emerging strategies whereby targeting metabolism can shape the T cell response.

Publication types

  • Review

MeSH terms

  • Amino Acids / metabolism
  • Animals
  • Autoimmune Diseases / drug therapy
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / metabolism
  • Autoimmunity / drug effects
  • Autoimmunity / immunology
  • Cell Differentiation / drug effects
  • Cell Differentiation / immunology*
  • Cellular Microenvironment / drug effects
  • Cellular Microenvironment / immunology
  • Energy Metabolism* / drug effects
  • Glycolysis / drug effects
  • Graft Rejection / drug therapy
  • Graft Rejection / immunology
  • Graft Rejection / metabolism
  • Humans
  • Immunotherapy
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology*
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Molecular Targeted Therapy
  • Signal Transduction / drug effects
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism*
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Amino Acids
  • TOR Serine-Threonine Kinases