Effect of TIM-3 Blockade on the Immunophenotype and Cytokine Profile of Murine Uterine NK Cells

被引:17
作者
Tripathi, Sudipta [1 ]
Chabtini, Lola [1 ]
Dakle, Pranal J. [1 ]
Smith, Brian [1 ]
Akiba, Hisaya [2 ]
Yagita, Hideo [2 ]
Guleria, Indira [1 ]
机构
[1] Harvard Univ, Sch Med, Div Renal, Childrens Hosp Boston, Boston, MA 02163 USA
[2] Juntendo Univ, Dept Immunol, Tokyo, Japan
来源
PLOS ONE | 2015年 / 10卷 / 04期
基金
美国国家卫生研究院;
关键词
NATURAL-KILLER-CELLS; METRIAL GLAND-CELLS; INNATE IMMUNE CELLS; CHRONIC HEPATITIS-B; SUPPRESSOR-CELLS; RECEPTORS; PREGNANCY; DIFFERENTIATION; REPERTOIRE; MICE;
D O I
10.1371/journal.pone.0123439
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
NK cells are the most abundant lymphocyte population in the feto-maternal interface during gestation. The uterine NK cells (uNK) are transient, have a unique immunophenotype and produce a number of cytokines. These cytokines play an important role in establishment and maintenance of vascular remodeling and tolerance associated with successful pregnancy. The uNK cells also express TIM-3 during gestation and blockade of TIM-3 expression results in fetal loss in mice. In this study we determined the effect of TIM-3 blockade on uNK cells. Specifically we observed surface receptor phenotype and cytokine production by uNK cells following TIM-3 blockade. Our results show that TIM-3 plays a role in regulating the uNK cells and contributes to the maintenance of tolerance at the feto-maternal interface.
引用
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页数:19
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