Generation of adaptive regulatory T cells by alloantigen is required for some but not all transplant tolerance protocols

Transplantation. 2011 Apr 15;91(7):707-13. doi: 10.1097/TP.0b013e31820e50b3.

Abstract

Background: Because CD4CD25Foxp3 regulatory T cells (Tregs) are essential for the maintenance of self-tolerance, significant interest surrounds the developmental cues for thymic-derived natural Tregs (nTregs) and periphery-generated adaptive Tregs (aTregs). In the transplant setting, the allograft may play a role in the generation of alloantigen-specific Tregs, but this role remains undefined. We examined whether the immune response to a transplant allograft results in the peripheral generation of aTregs.

Methods: To identify generation of aTregs, purified graft-reactive CD4CD25 T cells were adoptively transferred to mice-bearing skin allograft. To demonstrate that aTregs are necessary for tolerance, DBA/2 skin was transplanted onto C57BL/6-RAG-1-deficient recipients adoptively transferred with purified sorted CD4CD25 T cells; half of the recipients undergo tolerance induction treatment.

Results: By tracking adoptively transferred cells, we show that purified graft-reactive CD4CD25 T lymphocytes up-regulate Foxp3 in mice receiving skin allografts in the absence of any treatment. Interestingly, cotransfer of antigen-specific nTregs suppresses the up-regulation of Foxp3 by inhibiting the proliferation of allograft-responsive T cells. In vitro data are consistent with our in vivo data-Foxp3 cells are generated on antigen activation, and this generation is suppressed on coculture with antigen-specific nTregs. Finally, blocking aTreg generation in grafted, rapamycin-treated mice disrupts alloantigen-specific tolerance induction. In contrast, blocking aTreg generation in grafted mice treated with nondepleting anti-CD4 plus anti-CD40L antibodies does not disrupt graft tolerance.

Conclusions: We conclude that graft alloantigen stimulates the de novo generation of aTregs, and this generation may represent a necessary step in some but not all protocols of tolerance induction.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • CD40 Antigens / physiology
  • CD40 Ligand / physiology
  • Forkhead Transcription Factors / genetics
  • Interleukin-2 / pharmacology
  • Isoantigens / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Sirolimus / pharmacology
  • T-Lymphocytes, Regulatory / physiology*
  • Transforming Growth Factor beta / pharmacology
  • Transplantation Tolerance*
  • Transplantation, Homologous

Substances

  • CD40 Antigens
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Interleukin-2
  • Isoantigens
  • Transforming Growth Factor beta
  • CD40 Ligand
  • Sirolimus