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One naive T cell, multiple fates in CD8+ T cell differentiation
Journal article   Open access   Peer reviewed

One naive T cell, multiple fates in CD8+ T cell differentiation

C. Gerlach, J.W.J. van Heijst, E. Swart, D. Sie, N. Armstrong, R.M. Kerkhoven, D. Zehn, M.J. Bevan, K. Schepers and T.N.M. Schumacher
Journal of Experimental Medicine, Vol.207(6), pp.1235-1246
2010
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Abstract

The mechanism by which the immune system produces effector and memory T cells is largely unclear. To allow a large-scale assessment of the development of single naive T cells into different subsets, we have developed a technology that introduces unique genetic tags (barcodes) into naive T cells. By comparing the barcodes present in antigen-specific effector and memory T cell populations in systemic and local infection models, at different anatomical sites, and for TCR–pMHC interactions of different avidities, we demonstrate that under all conditions tested, individual naive T cells yield both effector and memory CD8+ T cell progeny. This indicates that effector and memory fate decisions are not determined by the nature of the priming antigen-presenting cell or the time of T cell priming. Instead, for both low and high avidity T cells, individual naive T cells have multiple fates and can differentiate into effector and memory T cell subsets.

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.6 Immunology
1.6.127 T Cell Regulation
Web Of Science research areas
Immunology
Medicine, Research & Experimental
ESI research areas
Immunology
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