CD8+CD28- T cells:: Certainties and uncertainties of a prevalent human T-cell subset

被引:65
|
作者
Arosa, FA
机构
[1] Inst Mol & Cell Biol, Lab Mol Immunol, P-4150180 Oporto, Portugal
[2] Abel Salazar Inst Biomed Sci, Oporto, Portugal
来源
IMMUNOLOGY AND CELL BIOLOGY | 2002年 / 80卷 / 01期
关键词
CD8(+) T cells; CD28; downmodulation; epithelial cells; homeostasis; major histocompatibility complex-class I;
D O I
10.1046/j.1440-1711.2002.01057.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human peripheral blood CD8(+) T cells comprise cells that are in different states of differentiation and under the control of complex homeostatic processes. In a number of situations ranging from chronic inflammatory conditions and infectious diseases to ageing, immunodeficiency, iron overload and heavy alcohol intake, major phenotypic changes, usually associated with an increase in CD8(+) T cells lacking CD28 expression, take place. CD8(+)CD28(-) T cells are characterized by a low proliferative capacity to conventional stimulation in vitro and by morphological and functional features of activated/memory T cells. Although the nature of the signals that give origin to this T-cell subset is uncertain, growing evidence argues for the existence of an interplay between epithelial cells, molecules with the MHC-class I fold and CD8(+) T cells. The possibility that the generation of CD8(+)CD28(-) cells is the combination of TCR/CD3zeta- and regulatory factor-mediated signals as a result of the sensing of modifications of the internal environment is discussed.
引用
收藏
页码:1 / 13
页数:13
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