4.7 Review

The spectrum of T cell metabolism in health and disease

Journal

NATURE REVIEWS IMMUNOLOGY
Volume 18, Issue 1, Pages 19-34

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nri.2017.99

Keywords

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Categories

Funding

  1. French Ligue contre le Cancer (equipe labellisee)
  2. Agence National de la Recherche (ANR) - Projets blancs
  3. ANR
  4. ERA-Net for Research on Rare Diseases
  5. Association pour la recherche sur le cancer (ARC)
  6. Canceropole Ile-de-France
  7. Institut National du Cancer (INCa)
  8. Institut Universitaire de France
  9. Fondation pour la Recherche Medicale (FRM)
  10. European Commission (ArtForce)
  11. European Research Council (ERC)
  12. LeDucq Foundation
  13. LabEx Immuno Oncology
  14. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  15. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  16. Paris Alliance of Cancer Research Institutes (PACRI)
  17. Department of Radiation Oncology of Weill Cornell Medical College (New York, USA)
  18. Sotio a.c. (Prague, Czech Republic)
  19. Swiss National Science Foundation (SNSF) [310030_153059, 31003A_172848, CRSII3_160766]
  20. Gebert Ruf Foundation [GRS-058/14]

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In healthy individuals, metabolically quiescent T cells survey lymph nodes and peripheral tissues in search of cognate antigens. During infection, T cells that encounter cognate antigens are activated and - in a context-specific manner - proliferate and/or differentiate to become effector T cells. This process is accompanied by important changes in cellular metabolism (known as metabolic reprogramming). The magnitude and spectrum of metabolic reprogramming as it occurs in T cells in the context of acute infection ensure host survival. By contrast, altered T cell metabolism, and hence function, is also observed in various disease states, in which T cells actively contribute to pathology. In this Review, we introduce the idea that the spectrum of immune cell metabolic states can provide a basis for categorizing human diseases. Specifically, we first summarize the metabolic and interlinked signalling requirements of T cells responding to acute infection. We then discuss how metabolic reprogramming of T cells is linked to disease.

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