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Life after the thymus: CD31+ and CD31- human naive CD4+ T-cell subsets
被引:250
|作者:
Kohler, Siegfried
[1
]
Thiel, Andreas
[1
,2
]
机构:
[1] Deutsch Rheuma Forschungszentrum Berlin, Clin Immunol Grp, D-10117 Berlin, Germany
[2] Berlin Brandenburg Ctr Regenerat Therapies, Berlin, Germany
来源:
关键词:
HOMEOSTATIC PROLIFERATION;
TCR REPERTOIRE;
CLASS-II;
IN-VIVO;
MULTIPLE-SCLEROSIS;
FLOW-CYTOMETRY;
RECEPTOR;
ADHESION;
SURVIVAL;
PECAM-1;
D O I:
10.1182/blood-2008-02-139154
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
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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页码:769 / 774
页数:6
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