Tcf1+ cells are required to maintain the inflationary T cell pool upon MCMV infection

Suzanne P M Welten, Alexander Yermanos, Nicolas S Baumann, Franziska Wagen, Nathalie Oetiker, Ioana Sandu, Alessandro Pedrioli, Jennifer D Oduro, Sai T Reddy, Luka Cicin-Sain, Werner Held, Annette Oxenius*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Cytomegalovirus-based vaccine vectors offer interesting opportunities for T cell-based vaccination purposes as CMV infection induces large numbers of functional effector-like cells that accumulate in peripheral tissues, a process termed memory inflation. Maintenance of high numbers of peripheral CD8 T cells requires continuous replenishment of the inflationary T cell pool. Here, we show that the inflationary T cell population contains a small subset of cells expressing the transcription factor Tcf1. These Tcf1+ cells resemble central memory T cells and are proliferation competent. Upon sensing viral reactivation events, Tcf1+ cells feed into the pool of peripheral Tcf1- cells and depletion of Tcf1+ cells hampers memory inflation. TCR repertoires of Tcf1+ and Tcf1- populations largely overlap, with the Tcf1+ population showing higher clonal diversity. These data show that Tcf1+ cells are necessary for sustaining the inflationary T cell response, and upholding this subset is likely critical for the success of CMV-based vaccination approaches.

Original languageEnglish
Article number2295
Pages (from-to)2295
JournalNature Communications
Volume11
Issue number1
DOIs
Publication statusPublished - 8 May 2020
Externally publishedYes

Keywords

  • Animals
  • CD8-Positive T-Lymphocytes/immunology
  • Cell Proliferation
  • Clone Cells
  • Herpesviridae Infections/immunology
  • Immunologic Memory
  • Interferon Type I/metabolism
  • Interleukin-12/metabolism
  • Mice, Inbred C57BL
  • Muromegalovirus/physiology
  • Phenotype
  • T Cell Transcription Factor 1/metabolism
  • T-Lymphocytes/immunology

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