Early in life, thymic export establishes the size and the diversity of the human naive T-cell pool. Yet, on puberty thymic activity drastically decreases. Because the overall size of the naive T-cell pool decreases only marginally during ageing, peripheral postthymic expansion of naive T cells has been postulated to account partly for the maintenance of T-cell immunity in adults. So far, the analysis of these processes had been hampered by the inability to distinguish recent thymic emigrants from proliferated, peripheral, naive T cells. However, recently, CD31 has been introduced as a marker to distinguish 2 subsets of naive CD4(+) T cells with distinct T-cell receptor excision circle (TREC) content in the peripheral blood of healthy humans. Here, we review studies that have characterized TREChi CD31(+) thymicnaive CD4(+) T cells and have accordingly used the assessment of this distinct subset of naive CD4(+) T cells as a correlate of thymic activity. We will discuss further potential clinical applications and how more research on CD31(+) thymic naive and CD31(+) centralnaive CD4(+) T cells may foster our knowledge of the impact of thymic involution on immune competence. (Blood. 2009; 113: 769-774)
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Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX3 9DU, EnglandUniv Oxford, Sir William Dunn Sch Pathol, Oxford OX3 9DU, England
Shale, Matthew
Schiering, Chris
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Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX3 9DU, EnglandUniv Oxford, Sir William Dunn Sch Pathol, Oxford OX3 9DU, England
Schiering, Chris
Powrie, Fiona
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Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX3 9DU, England
Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Med, Translat Gastroenterol Unit,Expt Med Div, Oxford OX3 9DU, EnglandUniv Oxford, Sir William Dunn Sch Pathol, Oxford OX3 9DU, England