Induction of alloreactive CD4 T cell tolerance in molecular chimeras: a possible role for regulatory T cells

J Immunol. 2006 Mar 15;176(6):3410-6. doi: 10.4049/jimmunol.176.6.3410.

Abstract

Induction of molecular chimerism following reconstitution of mice with autologous bone marrow cells expressing a retrovirally encoded allogeneic MHC class I Ag results in donor-specific tolerance. To investigate the mechanism by which CD4 T cells that recognize allogeneic MHC class I through the indirect pathway of Ag presentation are rendered tolerant in molecular chimeras, transgenic mice expressing a TCR on CD4 T cells specific for peptides derived from K(b) were used. CD4 T cells expressing the transgenic TCR were detected in mice reconstituted with bone marrow cells transduced with retroviruses carrying the gene encoding H-2K(b), albeit detection was at lower levels than in mice receiving mock-transduced bone marrow. Despite the presence of CD4 T cells expressing an alloreactive TCR, mice receiving H-2K(b)-transduced bone marrow permanently accepted K(b) disparate skin grafts. CD4+CD25+ T cells from mice reconstituted with H-2K(b)-transduced bone marrow prevented rejection of K(b) disparate skin grafts when adoptively transferred into immunodeficient mice along with effector T cells, suggesting that induction of molecular chimerism leads to the generation of donor specific regulatory T cells, which may be involved in preventing alloreactive CD4 T cell responses that lead to rejection.

Publication types

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

MeSH terms

  • Animals
  • Antigen Presentation / immunology
  • Bone Marrow / immunology
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Differentiation
  • Cell Transplantation
  • Cells, Cultured
  • Chimera / immunology*
  • Female
  • Gene Deletion
  • Immune Tolerance / immunology*
  • Isoantigens / immunology*
  • Mice
  • Mice, Transgenic
  • Models, Immunological
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / immunology
  • Receptors, Antigen, T-Cell / metabolism
  • Survival Rate
  • T-Lymphocytes, Regulatory / immunology*
  • Thymus Gland / metabolism
  • Transplantation, Homologous

Substances

  • Isoantigens
  • Receptors, Antigen, T-Cell