Killing activity of human umbilical cord blood-derived TCRValpha24(+) NKT cells against normal and malignant hematological cells in vitro: a comparative study with NK cells or OKT3 activated T lymphocytes or with adult peripheral blood NKT cells

Cancer Immunol Immunother. 2002 Mar;51(1):1-8. doi: 10.1007/s00262-001-0246-2. Epub 2001 Dec 12.

Abstract

Purpose: We aimed to determine the effects of human umbilical cord blood (UCB)-derived natural killer T (NKT) cells as immunological effectors against hematological malignancies, as well as auto- or allo-dendritic cells (DCs) or EB transformed cell lines (EBCLs).

Materials: TCRValpha24(+) Vbeta11(+) UCB- or PB-NKT cells were isolated by sorting and activated by alpha-galactosylceramide-pulsed autologous DCs. UCB-NK cells were induced from CD34(+) cells by stem cell factor plus IL-15. UCB-T cells were primarily activated by anti-CD3 monoclonal antibody. All those effectors were cultured with IL-2 (100 U/ml), and their cytotoxic activities were evaluated by (51)Cr-release assay. UCB-NKT cells were cultured with IL-12, IL-18 or higher dose of IL-2 (1000 U/ml), and again tested for the cytotoxicity against selected targets.

Results: UCB-NKT cells exhibited a pattern of killing activity against various hematological malignancies similar to that of UCB-NK cells, but could not kill K562, which was a vulnerable target for NK cells. The level of activity was quite similar to that of PB-NKT cells. In contrast, OKT-3-activated UCB-T lymphocytes showed a stronger and wider spectrum of killing compared with UCB-NK or NKT cells. IL-12, IL-18 or a higher dose of IL-2 upregulated the activity; however several targets, including fresh leukemic cells, still remained resistant. NKT cells killed auto- or allo-DCs at a level similar to that of T cells, but could not kill allo-EBCLs, which were efficiently killed by T cells. While NK cells showed only marginal or no killing against DC or EBCLs.

Discussion: The anti-cancer activity of human NKT cells depends on the concentrations or the combination of Th1-cytokines. Basically, those cells might not be contributing to the immune surveillance of hematological malignancies, as shown by a relatively low cytotoxicity against malignant cells, together with the quite strong killing against auto-DCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD1 / analysis
  • Antigens, CD1 / immunology
  • Antigens, CD1d
  • Antigens, Neoplasm / analysis
  • Antigens, Neoplasm / immunology
  • Autoimmunity
  • Blood Cells
  • Cell Line, Transformed
  • Cell Separation
  • Cytotoxicity, Immunologic / drug effects
  • Dendritic Cells / immunology
  • Dose-Response Relationship, Drug
  • Fetal Blood / cytology*
  • Fetal Blood / immunology
  • Flow Cytometry
  • Galactosylceramides / immunology
  • Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor
  • Hematologic Neoplasms / immunology
  • Hematologic Neoplasms / pathology
  • Humans
  • Interleukin-12 / pharmacology
  • Interleukin-18 / pharmacology
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology*
  • Lymphocyte Activation / drug effects
  • Muromonab-CD3 / pharmacology*
  • Neoplastic Stem Cells
  • Receptors, Antigen, T-Cell, alpha-beta / genetics*
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / immunology*
  • Tumor Cells, Cultured

Substances

  • Antigens, CD1
  • Antigens, CD1d
  • Antigens, Neoplasm
  • CD1D protein, human
  • Galactosylceramides
  • Interleukin-18
  • Muromonab-CD3
  • Receptors, Antigen, T-Cell, alpha-beta
  • Interleukin-12