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 language | English |
|---|---|
| Article number | 2295 |
| Pages (from-to) | 2295 |
| Journal | Nature Communications |
| Volume | 11 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 8 May 2020 |
| Externally published | Yes |
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