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Childrens Research Centre, Our Ladys Hospital for Sick Children, Dublin, Ireland; and
Conway Institute for Biomolecular and Biomedical Research, University College, Dublin, Ireland.
This study shows that, in humans at birth, circulating T cells
represent recent thymic emigrants (RTEs) as reflected in their high
level of expression of TCR excision circles. RTEs express
"thymocyte-like" characteristics with regard to rapid rate of
apoptosis. In the presence of common
-chain cytokines, in particular
IL-7, they show enhanced potential to survive, entry into cell cycle,
and proliferation. Although common
-chain cytokines were also potent
antiapoptotic stimuli for mature adult-derived naive
CD4+CD45RA+ T cells, these cells were
refractory to IL-7-induced expansion in vitro. RTEs cultured with IL-7
could not reinduce recombination-activating gene-2 gene expression in
vitro. These data suggest that postthymic naive T cells in the
periphery during early life are at a unique stage in ontogeny as RTEs,
during which they can undergo homeostatic regulation including
expansion and survival in an Ag-independent manner while maintaining
their preselected TCR repertoire.
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