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

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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University of Melbourne Researchers

Grants

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.).