Redirection of CMV-specific CTL towards B-CLL via CD20-targeted HLA/CMV complexes

Leukemia. 2006 Jun;20(6):1096-102. doi: 10.1038/sj.leu.2404185.

Abstract

B-cell chronic lymphocytic leukaemia (B-CLL) is a slowly progressing malignancy of CD5(+) B cells, for which at present no curative treatment is available. In our current study, we apply a novel bridging reagent to redirect cytomegalovirus (CMV)-specific cytotoxic T lymphocytes (CTL) to target B-CLL. A streptavidin-fused anti-CD20 single-chain variable fragment (scFv) is used in combination with biotinylated MHC class I molecules containing CMV pp65 peptide (HLA/CMV). We demonstrate that B-CLL cells coated with this CD20-HLA/CMV complex can be lysed by autologous CMV-specific CTL with similar efficiency as B-CLL cells directly loaded with CMV peptide. Killing is HLA restricted and occurs at scFv CD20 concentrations of >/=100 ng ml(-1) and HLA/CMV concentrations of >/=20 ng ml(-1). Furthermore, complex-coated B-CLL cells induce both proliferation and cytokine production (interferon gamma, tumour necrosis factor alpha and macrophage inflammatory protein-1 beta) in CMV-specific CD8(+) T cells. Hereby, a necessary step towards possible application of CD20-HLA/CMV complexes for immunotherapy of B-cell malignancies is constituted.

MeSH terms

  • Antigens, CD20 / biosynthesis
  • Antigens, CD20 / immunology*
  • Cell Proliferation
  • Cytokines / biosynthesis
  • Cytomegalovirus / immunology*
  • Cytotoxicity Tests, Immunologic
  • HLA Antigens / immunology*
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell / diagnosis
  • Leukemia, Lymphocytic, Chronic, B-Cell / immunology*
  • Multiprotein Complexes / immunology
  • Peptides / immunology*
  • T-Lymphocytes, Cytotoxic / immunology*
  • Tumor Cells, Cultured

Substances

  • Antigens, CD20
  • Cytokines
  • HLA Antigens
  • Multiprotein Complexes
  • Peptides