Antigen persistence and time of T-cell tolerization determine the efficacy of tolerization protocols for prevention of skin graft rejection

Nat Med. 1998 Sep;4(9):1015-9. doi: 10.1038/2001.

Abstract

We studied antigen-specific T-cell tolerization therapy using skin transplantation across a defined minor histocompatibility antigen difference. Specific tolerization protocols using short-lived peptide or long-lived spleen cells presenting the peptide as antigen prevented graft rejection without immunosuppression when started before or as long as 10 days after transplantation. Peptide-induced T-cell tolerance was transient, and antigen presentation by the graft was not sufficient to maintain tolerance. In contrast, transfer of antigen-expressing lymphoid cells induced long-lasting tolerance correlating with donor cell chimerism. These findings show that antigen-specific tolerization can induce graft acceptance even when begun after transplantation and that long-term graft survival depends on persistence of the tolerizing antigen.

MeSH terms

  • Animals
  • Antigens / immunology
  • Antigens, Viral*
  • Cell Line
  • Epitopes, T-Lymphocyte / genetics
  • Epitopes, T-Lymphocyte / immunology*
  • Glycoproteins / genetics
  • Glycoproteins / immunology
  • Graft Rejection / immunology*
  • Immune Tolerance*
  • Lymphocytic choriomeningitis virus / genetics
  • Lymphocytic choriomeningitis virus / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Peptide Fragments / genetics
  • Peptide Fragments / immunology
  • Skin Transplantation / immunology*
  • T-Lymphocytes, Cytotoxic / immunology*
  • Time Factors
  • Viral Proteins*

Substances

  • Antigens
  • Antigens, Viral
  • Epitopes, T-Lymphocyte
  • Glycoproteins
  • Peptide Fragments
  • Viral Proteins
  • glycoprotein peptide 33-41, Lymphocytic choriomeningitis virus