Contrasting CD25hiCD4+T cells/FOXP3 patterns in chronic rejection and operational drug-free tolerance

Transplantation. 2006 Feb 15;81(3):398-407. doi: 10.1097/01.tp.0000203166.44968.86.

Abstract

Background: Although immunosuppression withdrawal in kidney recipients usually leads to rejection, in some patients it does not, leading to a state of clinical operational tolerance.

Methods: We compared these highly contrasted situations by analyzing blood cell phenotype and transcriptional patterns in drug-free spontaneously tolerant kidney recipients, recipients with chronic rejection, recipients with stable graft function under standard or minimal immunosuppression and healthy individuals

Results: The blood cell phenotype of clinically tolerant patients did not differ from that of healthy individuals. In contrast, recipients with chronic rejection had significantly less CD25hiCD4+T cells and lower levels of FOXP3 transcripts compared with clinically tolerant recipients. Patients with chronic rejection also displayed CD25-CD4+T cells expressing NKG2D+CD94+ and CD57+CD27-CD28- cytotoxic-associated markers (P<0.05).

Conclusion: These data show that whereas clinically tolerant recipients displayed normal levels of CD25hiCD4+T cells and FOXP3 transcripts, chronic rejection is associated with a decrease in CD25hiCD4+T cells and FOXP3 transcripts, suggesting that clinically "operational tolerance" may be due to a maintained phenomenon of natural tolerance that is lacking in patients with chronic rejection.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • B-Lymphocytes / immunology
  • CD4 Antigens / analysis
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / immunology
  • Female
  • Forkhead Transcription Factors / genetics*
  • Graft Rejection / genetics*
  • Graft Rejection / immunology*
  • Graft Rejection / therapy
  • Humans
  • Immune Tolerance / genetics
  • Immune Tolerance / immunology
  • Immunosuppression Therapy
  • Kidney Transplantation*
  • Male
  • Middle Aged
  • Receptors, Interleukin-2 / analysis*
  • Receptors, Interleukin-2 / immunology
  • T-Lymphocyte Subsets / immunology
  • Transcription, Genetic

Substances

  • CD4 Antigens
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Receptors, Interleukin-2