Braudeau Cécile, Racape Maud, Giral Magali, Louis Stéphanie, Moreau Anne, Berthelot Laureline, Heslan Michèle, Ashton-Chess Joanna, Soulillou Jean-Paul, Brouard Sophie
INSERM, U643, Nantes, F44000, France.
Transpl Int. 2007 Oct;20(10):845-55. doi: 10.1111/j.1432-2277.2007.00537.x.
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.
慢性排斥反应(CR)是导致长期移植物丢失的主要原因,而诱导免疫耐受可避免这种情况。我们之前发现,与具有手术诱导免疫耐受的患者、移植肾功能稳定的患者及健康志愿者(HV)相比,发生CR的肾移植患者外周血CD4(+)CD25(high) T细胞数量较少。在此,我们重点研究了这些患者血液中CD4(+)CD25(high) T细胞的特征,包括其调节性T细胞(Treg)基因叉头框P3(FOXP3)的表达及其抑制功能。我们发现,CR与具有正常调节特征的CD4(+)CD25(high)FOXP3(+)T细胞数量减少有关,而移植肾的成功接受则与数量类似于健康志愿者的CD4(+)CD25(high)FOXP3(+)T细胞有关。这些数据表明,Treg的数量而非其内在抑制能力,可能有助于决定肾移植的长期转归。