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

Transpl Int. 2007 Oct;20(10):845-55. doi: 10.1111/j.1432-2277.2007.00537.x.

Abstract

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.

MeSH terms

  • Adult
  • Aged
  • CD4 Antigens / immunology*
  • Cell Proliferation
  • Disease Progression
  • Female
  • Follow-Up Studies
  • Forkhead Transcription Factors / immunology*
  • Graft Rejection / blood
  • Graft Rejection / immunology*
  • Graft Rejection / pathology
  • Humans
  • Immune Tolerance
  • Immunity, Cellular / immunology*
  • Interleukin-2 Receptor alpha Subunit / immunology*
  • Kidney Transplantation / immunology*
  • Kidney Transplantation / pathology
  • Male
  • Middle Aged
  • Prognosis
  • T-Lymphocytes / immunology*
  • Time Factors

Substances

  • CD4 Antigens
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Interleukin-2 Receptor alpha Subunit