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

Nat Commun. 2020 May 8;11(1):2295. doi: 10.1038/s41467-020-16219-3.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

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

Substances

  • Interferon Type I
  • T Cell Transcription Factor 1
  • Interleukin-12