NDT Advance Access originally published online on June 25, 2007
Nephrology Dialysis Transplantation 2007 22(11):3221-3227; doi:10.1093/ndt/gfm361
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Treatment with recombinant human erythropoietin is associated with rejuvenation of CD8+ T cell compartment in chronic renal failure patients
bska-
lizie
2
liwski1
aw Rutkowski2
1Department of Histology and Immunology and 2Department of Nephrology, Transplantology and Internal Diseases, Medical University of Gda
sk, Poland
Correspondence and offprint requests to: Piotr Trzonkowski, MD, PhD, Department of Histology and Immunology, Medical University of Gda
sk, Ul. D
binki 1, 80-211 Gda
sk, Poland. Email: ptrzon{at}amg.gda.pl; piotr.trzonkowski{at}surgery.oxford.ac.uk
| Abstract |
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Background. A growing body of evidence suggests an impact of rHuEpo on the immune system.
Methods. We assessed the impact of recombinant human erythropoietin (rHuEpo) on the immunity of 11 chronic renal failure patients who did not require haemodialysis. Naïve (Tn), central (Tcm) and effectory memory (Tcm, Tem, TemRA) subsets of CD8+ T cells, memory-CMV-specific CD8+ T cells, titres of anti-CMV antibodies and activity of NK cells were evaluated during the first year of rHuEpo administration.
Results. While the number of CD8 T cells did not change, significant change was found in their proportions. Percentage of Tn cells increased at the expense of Tcm cells. Appearing Tn cells were CD28+ increasing the total pool of CD28+ T cells. Together with decreasing number, Tcm cells changed to mainly CD28– Tcm cells. A move towards the naïve compartment was also confirmed as the level of memory-CMV-specific CD8+ T cells decreased. Humoral immunity analysed as titres of anti-CMV antibodies as well as innate immunity measured as cytotoxicity of NK cells did not change during the follow-up.
Conclusions. We found that the administration of rHuEpo caused rejuvenation of cellular CD8+ T-dependent immunity in our patients.
Keywords: CD8+ T cells; CD28- T cells; central memory T cells; chronic renal failure; naïve T cells; recombinant human erythropoietin
Received for publication: 25. 1.07
Accepted in revised form: 11. 5.07