Induction of central tolerance by mature T cells

J Immunol. 2004 Dec 15;173(12):7217-22. doi: 10.4049/jimmunol.173.12.7217.

Abstract

Induction of immunological tolerance is highly desirable for the treatment and prevention of autoimmunity, allergy, and organ transplant rejection. Adoptive transfer of MHC class I disparate mature T cells at the time of reconstitution of mice with syngeneic bone marrow resulted in specific tolerance to allogeneic skin grafts that were matched to the T cell donor strain. Mature allogeneic T cells survived long-term in reconstituted hosts and were able to re-enter the thymus. Analysis of T cell development using transgenic mice expressing an alloantigen-reactive TCR revealed that expression of allogeneic MHC class I on adoptively transferred mature T cells mediated negative selection of developing alloreactive T cells in the thymus. Thus, mature allogeneic T cells are able to mediate central deletion of alloreactive cells and induce transplantation tolerance without the requirement for any other alloantigen-expressing cell type.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adoptive Transfer
  • Animals
  • B-Lymphocyte Subsets / cytology
  • B-Lymphocyte Subsets / immunology
  • B-Lymphocyte Subsets / transplantation
  • Bone Marrow Transplantation / immunology
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • Cell Differentiation / genetics
  • Cell Differentiation / immunology
  • Cell Survival / genetics
  • Cell Survival / immunology
  • Female
  • Graft Rejection / genetics
  • Graft Rejection / immunology
  • H-2 Antigens / biosynthesis
  • H-2 Antigens / genetics
  • Histocompatibility Testing
  • Mice
  • Mice, Inbred CBA
  • Mice, Transgenic
  • Radiation Chimera
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / transplantation*
  • Thymus Gland / cytology
  • Thymus Gland / immunology
  • Transplantation Conditioning / methods
  • Transplantation Tolerance* / genetics

Substances

  • H-2 Antigens
  • H-2Kb protein, mouse