Login / Signup

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

Suzanne P M WeltenAlexander YermanosNicolas S BaumannFranziska WagenNathalie OetikerIoana SanduAlessandro PedrioliJennifer D OduroSai T ReddyLuka Čičin ŠainWerner HeldAnnette Oxenius
Published in: Nature communications (2020)
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.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • transcription factor
  • signaling pathway
  • cell death
  • oxidative stress
  • machine learning
  • epstein barr virus
  • pi k akt
  • artificial intelligence
  • gene therapy