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

Authors :
Welten, Suzanne P. M.
Yermanos, Alexander
Baumann, Nicolas S.
Wagen, Franziska
Oetiker, Nathalie
Sandu, Ioana
Pedrioli, Alessandro
Oduro, Jennifer D.
Reddy, Sai T.
Cicin-Sain, Luka
Held, Werner
Oxenius, Annette
Source :
Nature Communications; 5/8/2020, Vol. 11 Issue 1, p1-14, 14p
Publication Year :
2020

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<superscript>+</superscript> cells resemble central memory T cells and are proliferation competent. Upon sensing viral reactivation events, Tcf1<superscript>+</superscript> cells feed into the pool of peripheral Tcf1<superscript>−</superscript> cells and depletion of Tcf1<superscript>+</superscript> cells hampers memory inflation. TCR repertoires of Tcf1<superscript>+</superscript> and Tcf1<superscript>−</superscript> populations largely overlap, with the Tcf1<superscript>+</superscript> population showing higher clonal diversity. These data show that Tcf1<superscript>+</superscript> 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. Upon infection with cytomegalovirus, CD8<superscript>+</superscript> T cells undergo prolific expansion in a process known as memory inflation. Here the authors define a population of Tcf1 expressing cells within the inflationary pool that is critical in fuelling this process. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
11
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
143113468
Full Text :
https://doi.org/10.1038/s41467-020-16219-3