Identification of Cytolytic CD161-CD56+ Regulatory CD8 T Cells in Human Peripheral Blood

被引:16
作者
Hu, Dan [1 ,2 ,3 ]
Weiner, Howard L. [1 ,3 ]
Ritz, Jerome [2 ,3 ]
机构
[1] Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Div Hematol Malignancies, Canc Vaccine Ctr, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
来源
PLOS ONE | 2013年 / 8卷 / 03期
基金
美国国家卫生研究院;
关键词
EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; NATURAL-KILLER-CELLS; DENDRITIC CELLS; SELF-TOLERANCE; EXPRESSION; SUBSET; CD27; STIMULATION; LYMPHOCYTES; BIOLOGY;
D O I
10.1371/journal.pone.0059545
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We previously developed methods for establishing CD8 regulatory T cell (Treg) clones from normal human peripheral blood and demonstrated that these clones were capable of killing T cell receptor (TCR)-activated autologous CD4 T cells. Based on phenotypic and functional characterization of the CD8 Treg clones, we have identified a corresponding population of endogenous CD8 Treg in normal human peripheral blood. These cells appear morphologically as large lymphocytes with abundant cytoplasm and have the following unique phenotype: CD3(+)CD8(+)CD161(-)CD56(+). The majority of CD8 Treg express CD45RA and CD62L with low or negative expression of CD45RO, CD25, CD27, CD28 and CCR7. The expression of CD94 and NKG2a on CD8 Treg was elevated compared to conventional CD8 T cells. Following in vitro activation, this T cell subset is capable of killing TCR-activated CD4 T cells. These studies identify an endogenous CD8 Treg population in humans and it will now be possible to characterize these cells in a variety of clinical conditions.
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页数:10
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