Donor lymphocyte infusion induces long-term donor-specific cardiac xenograft survival through activation of recipient double-negative regulatory T cells

J Immunol. 2005 Sep 1;175(5):3409-16. doi: 10.4049/jimmunol.175.5.3409.

Abstract

Previous studies have shown that pretransplant donor lymphocyte infusion (DLI) can enhance xenograft survival. However, the mechanism by which DLI induces xenograft survival remains obscure. Using T cell subset-deficient mice as recipients we show that CD4+, but not CD8+, T cells are necessary to mediate the rejection of concordant cardiac xenografts. Adoptive transfer of naive CD4+ T cells induces rejection of accepted cardiac xenografts in CD4-/- mice. This rejection can be prevented by pretransplant DLI in the absence of any other treatment. Furthermore, we demonstrate that DLI activates alphabeta-TCR+CD3+CD4-CD8- double-negative (DN) regulatory T (Treg) cells in xenograft recipients, and that DLI-activated DN Treg cells can inhibit the proliferation of donor-specific xenoreactive CD4+ T cells in vitro. More importantly, adoptive transfer of DLI-activated DN Treg cells from xenograft recipients can suppress the proliferation of xenoreactive CD4+ T cells and their ability to produce IL-2 and IFN-gamma in vivo. Adoptive transfer of DLI-activated DN Treg cells also prevents CD4+ T cell-mediated cardiac xenograft rejection in an Ag-specific fashion. These data provide direct evidence that DLI can activate recipient DN Treg cells, which can induce donor-specific long-term cardiac xenograft survival by suppressing the proliferation and function of donor-specific CD4+ T cells in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • CD4-Positive T-Lymphocytes / physiology
  • Cytokines / biosynthesis
  • Graft Rejection / etiology
  • Graft Survival*
  • Heart Transplantation / immunology*
  • Lymphocyte Activation*
  • Lymphocyte Transfusion*
  • Mice
  • Mice, Inbred C57BL
  • Rats
  • Rats, Inbred Lew
  • Rats, Inbred WF
  • Receptors, Interleukin-2 / analysis
  • T-Lymphocytes / immunology*
  • Tissue Donors*
  • Transplantation, Heterologous / immunology*

Substances

  • Cytokines
  • Receptors, Interleukin-2