CD8(+) minor histocompatibility antigen-specific cytotoxic T lymphocyte clones eliminate human acute myeloid leukemia stem cells

Proc Natl Acad Sci U S A. 1999 Jul 20;96(15):8639-44. doi: 10.1073/pnas.96.15.8639.

Abstract

Effective immunotherapy for human leukemia based on infusions of T lymphocytes requires the identification of effector T cells that target the leukemic stem cell. The transplantation of human acute myeloid leukemia into nonobese diabetic/severe combined immune deficient (SCID) mice has identified a rare leukemic progenitor termed the SCID leukemia-initiating cell, which is present in low frequency in the leukemic population and is essential for establishing leukemic hematopoiesis. Thus, this transplant model may be ideally suited to identify effector T cells with antileukemic activity. We report that CD8(+) cytotoxic T lymphocyte (CTL) clones specific for minor histocompatibility antigens inhibit the engraftment of human acute myeloid leukemia cells in nonobese diabetic/SCID mice and demonstrate that this inhibition is mediated by direct CTL recognition of SCID leukemia-initiating cells. These results indicate that CD8(+) minor histocompatibility antigen-specific CTL may be mediators of the graft-versus-leukemia effect associated with allogeneic hematopoietic cell transplantation and provide an experimental model to identify and select T cell clones for immunotherapy to prevent or treat relapse after allogeneic hematopoietic cell transplantation.

Publication types

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

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • Cell Transplantation
  • Clone Cells / immunology
  • Coculture Techniques
  • Cytotoxicity Tests, Immunologic
  • Flow Cytometry
  • Graft Rejection / immunology
  • Humans
  • Immunotherapy / methods
  • Leukemia, Myeloid / immunology*
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Minor Histocompatibility Antigens / immunology*
  • Stem Cells / immunology*
  • T-Lymphocytes, Cytotoxic / immunology*

Substances

  • Minor Histocompatibility Antigens