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Possible involvement of allogeneic antigens recognised by donor-derived CD4 + cytotoxic T cells in selective GVL effects after stem cell transplantation of patients with haematological malignancy

  • Maiko Matsushita
  • , Rie Yamazaki
  • , Hideyuki Ikeda
  • , Takehiko Mori
  • , Hidetoshi Sumimoto
  • , Tomonobu Fujita
  • , Shinichiro Okamoto
  • , Yasuo Ikeda
  • , Yutaka Kawakami

Research output: Contribution to journalArticlepeer-review

Abstract

Cytotoxic T lymphocyte (CTL) lines specific for allogeneic antigens were generated by in vitro stimulation of donor-derived peripheral blood mononuclear cells obtained from patients who received human leucocyte antigen (HLA)-matched allogeneic haematopoietic stem cell transplantation (HSCT). One of the allogeneic antigen-specific CD4 + CTL lines, CTL-A, generated from a patient with T cell acute lymphoblastic leukaemia, recognised HLA-DPB1*0501-positive Epstein-Barr virus-immortalised human B cell line (EBV-B cells), phytohaemagglutinin blasts and leukaemia cells, but not interferon-γ (IFN-γ) treated HLA-DPB1*0501-positive fibroblasts, indicating that this CD4 + T-cell line recognised a minor histocompatibility antigen (mHa) that is preferentially expressed in haematopoietic cells in an HLA-DPB1*0501-restricted manner. The other CD4 + CTL line, CTL-B, generated from a patient with chronic myeloid leukaemia, recognised mismatched HLA-DQB1*0303 on EBV-B cells and phytohaemagglutinin (PHA) blasts. Interestingly, this CTL line did not recognise IFN-γ-treated recipient's skin fibroblasts, as HLA-DQ was merely upregulated even after IFN-γ stimulation in non-haematopoietic cells including fibroblasts, endothelial cells and hepatocytes. These results suggest that these CD4 positive CTLs, specific for mismatch HLA-DQ and mHa that are preferentially expressed on haematopoietic cells, may play an important role in induction of selective graft-versus-leukaemia effect without development of graft-versus-host disease after allogeneic HSCT.

Original languageEnglish
Pages (from-to)56-65
Number of pages10
JournalBritish Journal of Haematology
Volume132
Issue number1
DOIs
Publication statusPublished - 2006 Jan

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • CD4 cytotoxic T cells
  • Graft-versus leukaemia effect
  • Minor histocompatibility antigens
  • Stem cell transplantation

ASJC Scopus subject areas

  • Hematology

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