Generation and administration of HA-1-specific T-cell lines for the treatment of patients with relapsed leukemia after allogeneic stem cell transplantation: a pilot study

Haematologica. 2012 Aug;97(8):1205-8. doi: 10.3324/haematol.2011.053371. Epub 2012 Apr 17.

Abstract

Since HA-1-specific T cells have been shown to make a significant contribution to the clinical responses in patients with relapsed leukemia, we investigated the feasibility of adoptive transfer of in vitro induced HA-1-specific CD8 positive T cells to patients with relapsed leukemia after allogeneic stem cell transplantation. The in vitro generation of clinical grade HA-1-specific T-cell lines from HA-1 negative donors was seen to be feasible and 3 patients were treated with HA-1-specific T-cell lines. No toxicity after infusion was observed. Although in one patient, during a period of stable disease, HA-1-specific T cells could be detected in the peripheral blood and bone marrow, these patients had no clear clinical response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer*
  • CD8-Positive T-Lymphocytes / immunology*
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Leukemia / immunology*
  • Leukemia / therapy*
  • Minor Histocompatibility Antigens / immunology*
  • Oligopeptides / immunology*
  • Pilot Projects
  • Recurrence
  • Transplantation, Homologous
  • Treatment Outcome

Substances

  • HA-1 antigen
  • Minor Histocompatibility Antigens
  • Oligopeptides