Variation in numbers of CD4+CD25highFOXP3+ T cells with normal immuno-regulatory properties in long-term graft outcome

被引:98
|
作者
Braudeau, Cecile
Racape, Maud
Giral, Magali
Louis, Stephanie
Moreau, Anne
Berthelot, Laureline
Heslan, Michele
Ashton-Chess, Joanna
Soulillou, Jean-Paul
Brouard, Sophie
机构
[1] INSERM, U643, F-44000 Nantes, France
[2] CHU Nantes, Inst Transplantat & Rech Translantat, ITERT, F-44000 Nantes, France
[3] Univ Nantes, Fac Med, F-44000 Nantes, France
[4] CHU Nantes, F-44000 Nantes, France
[5] Univ Nantes, Fac Med, F-44000 Nantes, France
关键词
chronic rejection; kidney; operational tolerance; regulatory cells; suppression; CHRONIC REJECTION; FOXP3; EXPRESSION; GENERATION; RECIPIENTS; INDUCTION; TOLERANCE; RAPAMYCIN; BLOOD;
D O I
10.1111/j.1432-2277.2007.00537.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Chronic rejection (CR) is a major cause of long-term graft loss that would be avoided by the induction of tolerance. We previously showed that renal transplant patients with CR have lower numbers of peripheral CD4(+)CD25(high) T cells than operationally tolerant patients, patients with stable graft function and healthy volunteers (HV). We explored here the profile of CD4(+)CD25(high) blood T cells in these patients focusing on their expression of the regulatory T cells (Treg) gene Forkhead Box P3 (FOXP3) and their suppressive function. We show that CR is associated with a decreased number of CD4(+)CD25(high)FOXP3(+)T cells with normal regulatory profile, whereas graft acceptance is associated with CD4(+)CD25(high)FOXP3(+)T cell numbers similar to HVs. These data suggest that Treg numbers, rather than their intrinsic suppressive capacity, may contribute to determining the long-term fate of renal transplants.
引用
收藏
页码:845 / 855
页数:11
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