Journal article
T cells maintain an exhausted phenotype after antigen withdrawal and population reexpansion
DT Utzschneider, A Legat, SA Fuertes Marraco, L Carrié, I Luescher, DE Speiser, D Zehn
Nature Immunology | NATURE PUBLISHING GROUP | Published : 2013
DOI: 10.1038/ni.2606
Abstract
During chronic infection, pathogen-specific CD8+ T cells upregulate expression of molecules such as the inhibitory surface receptor PD-1, have diminished cytokine production and are thought to undergo terminal differentiation into exhausted cells. Here we found that T cells with memory-like properties were generated during chronic infection. After transfer into naive mice, these cells robustly proliferated and controlled a viral infection. The reexpanded T cell populations continued to have the exhausted phenotype they acquired during the chronic infection. Thus, the cells underwent a form of differentiation that was stably transmitted to daughter cells. We therefore propose that during pers..
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Awarded by Swiss Vaccine Research Institute
Funding Acknowledgements
We thank S. Enouz, S. Oberle and M. Prlic for discussions and critical review of the manuscript; A. Oxenius (Institute of Microbiology, Swiss Federal Institute of Technology Zurich) for P14 alpha beta mice; P. Fink (University of Washington, Seattle) for V<INF>beta</INF>5 mice; and A. Wilson and H.R. MacDonald (Ludwig Center for Cancer Research, University of Lausanne) for antibodies specific to CD45.2 (clone 104) and CD45.1 (clone A20). Supported by the Swiss Vaccine Research Institute (D.Z.) and the Swiss National Science Foundation (CRSII3_141879 to D.Z. and D.E.S.).