Chronic graft versus host disease is associated with an immune response to autologous human leukocyte antigen-derived peptides

Transplantation. 2010 Sep 15;90(5):555-63. doi: 10.1097/TP.0b013e3181e86b58.

Abstract

Background: Chronic graft-versus-host disease (cGVHD) is a major complication of allogeneic bone marrow transplantation (BMT) the immunopathogenesis of which is not well understood. Humoral and cellular immunity are both implicated, patients express a range of autoantibodies, but the targets of cellular immunity are not well defined. Autologous human leukocyte antigen (HLA)-derived peptides constitute a significant proportion of the repertoire.

Methods: We have investigated the response to HLA-derived peptides after allogeneic BMT using gamma-interferon enzyme-linked immunospot assay (ELISPOT). We also studied the release of this gamma-interferon by flow cytometry in a subgroup of responsive patients.

Results: The peripheral blood mononuclear cell response was assessed by gamma-interferon ELISPOT in 42 BMT recipients (21 with cGVHD) and 30 healthy donors. Thirteen of 21 patients diagnosed with cGVHD responded to at least one HLA-derived peptide compared with 1 of 21 patients without cGVHD (62% vs. 5%, P<10) and 1 of 30 healthy donors. In all but one patient these peptides correspond with the sequences of autologous HLA. The median single peptide-specific response in ELISPOT was 43/10 peripheral blood mononuclear cells. In a subgroup studied by flow cytometry, gamma-interferon production to individual peptides occurred in 0.04% to 0.18% of CD4 T lymphocytes.

Conclusion: These observations identify HLA-derived peptides as targets of a cellular immune response in cGVHD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Marrow Transplantation / immunology*
  • Female
  • Graft vs Host Disease / etiology
  • Graft vs Host Disease / immunology*
  • HLA Antigens / immunology*
  • Histocompatibility Antigens Class I / immunology
  • Humans
  • Immunity, Cellular
  • Immunity, Humoral
  • Immunophenotyping / methods
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / blood
  • Leukemia / surgery
  • Lymphocytes / immunology
  • Male
  • Transplantation, Homologous / immunology

Substances

  • HLA Antigens
  • Histocompatibility Antigens Class I
  • Interferon-gamma