In vivo tracking of 'color-coded' effector, natural and induced regulatory T cells in the allograft response

被引:131
作者
Fan, Zhigang [1 ]
Spencer, Joel A. [2 ,3 ]
Lu, Yan [1 ]
Pitsillides, Costas M. [2 ,4 ]
Singh, Gurbakhshish [1 ]
Kim, Pilhan [5 ]
Yun, Seok H. [5 ]
Toxavidis, Vasilis [1 ]
Strom, Terry B. [1 ]
Lin, Charles P. [2 ]
Koulmanda, Maria [1 ]
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Transplant Inst, Sch Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Adv Microscopy Program, Ctr Syst Biol, Boston, MA 02215 USA
[3] Tufts Univ, Dept Biomed Engn, Ctr Sci & Technol, Medford, MA 02155 USA
[4] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[5] Harvard Univ, Sch Med,Adv Microscopy Program, Massachusetts Gen Hosp, Wellman Ctr Photomed,Dept Dermatol, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
TRANSPLANTATION TOLERANCE; INDUCTION; REJECTION; GENERATION; AUTOIMMUNE; APOPTOSIS; BALANCE; FOXP3;
D O I
10.1038/nm.2155
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Here we present methods to longitudinally track islet allograft-infiltrating T cells in live mice by endoscopic confocal microscopy and to analyze circulating T cells by in vivo flow cytometry. We developed a new reporter mouse whose T cell subsets express distinct, 'color-coded' proteins enabling in vivo detection and identification of effector T cells (T(eff) cells) and discrimination between natural and induced regulatory T cells (nT(reg) and iT(reg) cells). Using these tools, we observed marked differences in the T cell response in recipients receiving tolerance-inducing therapy (CD154-specific monoclonal antibody plus rapamycin) compared to untreated controls. These results establish real-time cell tracking as a powerful means to probe the dynamic cellular interplay mediating immunologic rejection or transplant tolerance.
引用
收藏
页码:718 / U125
页数:6
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