Journal article
The molecular bases of δ/αβ T cell-mediated antigen recognition
DG Pellicci, AP Uldrich, J Le Nours, F Ross, E Chabrol, SBG Eckle, R de Boer, RT Lim, K McPherson, G Besra, AR Howell, L Moretta, J McCluskey, MHM Heemskerk, S Gras, J Rossjohn, DI Godfrey
Journal of Experimental Medicine | Published : 2014
DOI: 10.1084/jem.20141764
Abstract
αβ and γδ T cells are disparate T cell lineages that can respond to distinct antigens (Ags) via the use of the αβ and γδ T cell Ag receptors (TCRs), respectively. Here we characterize a population of human T cells, which we term δ/αβ T cells, expressing TCRs comprised of a TCR-δ variable gene (Vδ1) fused to joining α and constant α domains, paired with an array of TCR-β chains. We demonstrate that these cells, which represent ~50% of all Vδ1+ human T cells, can recognize peptide-and lipid-based Ags presented by human leukocyte antigen (HLA) and CD1d, respectively. Similar to type I natural killer T (NKT) cells, CD1dlipid Ag-reactive δ/αβ T cells recognized α-galactosylceramide (α-GalCer); ho..
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Grants
Awarded by National Institute of General Medical Sciences
Funding Acknowledgements
This work was supported by the Australian Research Council (ARC; DP110104124, CE140100011, and LE110100106), the National Health and Medical Research Council of Australia (NHMRC; #1013667), the Cancer Council of Victoria (#1042866), and National Institutes of Health R01 grant (GM 087136). D.G. Pellicci is supported by an NHMRC Biomedical fellowship, A.P. Uldrich by an ARC Future Fellowship (FT140100278), S. Gras by an ARC Future Fellowship (FT120100416), D.I. Godfrey by an NHMRC Senior Principal Research Fellowship (#1020770), and J. Rossjohn by an NHMRC Australia Fellowship (AF50).