Altered Basal Lipid Metabolism Underlies the Functional Impairment of Naive CD8+ T Cells in Elderly Humans

  • Francesco Nicoli
  • , Mariela P. Cabral-Piccin
  • , Laura Papagno
  • , Eleonora Gallerani
  • , Mathieu Fusaro
  • , Victor Folcher
  • , Marion Dubois
  • , Emmanuel Clave
  • , Hélène Vallet
  • , Justin J. Frere
  • , Emma Gostick
  • , Sian Llewellyn-Lacey
  • , David A. Price
  • , Antoine Toubert
  • , Loïc Dupré
  • , Jacques Boddaert
  • , Antonella Caputo
  • , Riccardo Gavioli
  • , Victor Appay

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

Aging is associated with functional deficits in the naive T cell compartment, which compromise the generation of de novo immune responses against previously unencountered Ags. The mechanisms that underlie this phenomenon have nonetheless remained unclear. We found that naive CD8+ T cells in elderly humans were prone to apoptosis and proliferated suboptimally in response to stimulation via the TCR. These abnormalities were associated with dysregulated lipid metabolism under homeostatic conditions and enhanced levels of basal activation. Importantly, reversal of the bioenergetic anomalies with lipid-altering drugs, such as rosiglitazone, almost completely restored the Ag responsiveness of naive CD8+ T cells. Interventions that favor lipid catabolism may therefore find utility as adjunctive therapies in the elderly to promote vaccine-induced immunity against targetable cancers and emerging pathogens, such as seasonal influenza viruses and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).

Original languageEnglish
Pages (from-to)562-570
Number of pages9
JournalJournal of Immunology
Volume208
Issue number3
DOIs
StatePublished - 1 Feb 2022
Externally publishedYes

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