NDT Advance Access published online on February 4, 2009
Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfp005
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
End-stage renal failure and regulatory activities of CD4+CD25bright+FoxP3+ T-cells
1 Department of Internal Medicine 2 Department of General Surgery, Erasmus MC, University Medical Center Rotterdam, Dr Molewaterplein 50, 3015 GE Rotterdam, The Netherlands
Correspondence and offprint requests to: Carla C. Baan, Erasmus MC, University Medical Center Rotterdam, Dr Molewaterplein 50, Room Ee559, 3015 GE Rotterdam, The Netherlands. Tel: +31-10-7035420; Fax: +31-10-7044718; E-mail: c.c.baan{at}erasmusmc.nl
 |
Abstract |
|---|
Background. The defensive immune system in patients with end-stage renal failure is impaired at multiple levels. This state of immune incompetence is associated with continuous activation of the immune system. An additional explanation for this state of activation may be the disturbed function of CD4+CD25bright+FoxP3+ regulatory T-cells.
Methods. The phenotype and function of peripheral regulatory T-cells from patients with end-stage renal failure (N = 80) and healthy controls (N = 17) was studied by flow cytometry, RT-PCR and mixed lymphocyte reaction. Patients were on haemodialysis (N = 40), peritoneal dialysis (N = 26) or not treated with dialysis yet (N = 14). The latter group had a glomerular filtration rate of <20 ml/min/ 1.73 m2.
Results. The basal IL-2 mRNA level was high in patient-PBMC (P = 0.0002 versus healthy controls). The absolute number of CD4+CD25bright+ T-cells was low in patients (P < 0.05 versus healthy controls). Furthermore, proliferation of patient-PBMC upon allogeneic stimulation was impaired (P < 0.0001 versus healthy controls). The regulatory function of CD4+CD25bright+ T-cells was determined in the setting of direct allorecognition. First, the effect of depletion of CD25bright+ cells from patient-PBMC on proliferation was low. Second, co-culture of CD25bright+ cells with CD25neg/dim cells (1:10 ratio) showed impaired regulatory function (P < 0.001 versus healthy controls), which was especially pronounced in patients on dialysis. The FOXP3 mRNA level was also low upon stimulation (P = 0.0002 versus healthy controls).
Conclusions. In line with previous studies, we observed an overactivated but functionally compromised immune system in patients with end-stage renal failure. It now appears that in this setting, regulation by CD4+CD25bright+FoxP3+ T-cells is also impaired.
Keywords: dialysis; end-stage renal failure; FoxP3; patients; regulatory T-cells
Received for publication: 17. 4.08
Accepted in revised form: 29.12.08