Human recombinant interleukin-6 enhances antibody-dependent cellular cytotoxicity of human tumor cells mediated by human peripheral blood mononuclear cells

Cancer Immunol Immunother. 1991;34(1):9-16. doi: 10.1007/BF01741318.

Abstract

The effects of human recombinant interleukin-6 (hrIL-6) on antibody-dependent cellular cytotoxicity (ADCC) activity mediated by human peripheral blood mononuclear cells (PMNC) were investigated. Human PMNC were preincubated for 24 h with various concentrations of hrIL-6 and were used as effector cells in a 4-h 51Cr-release assay. The ability of hrIL-6 to augment ADCC was measured using anti-colorectal carcinoma mAbs D612, 17.1A and 31.1 (each directed against a distinct tumor antigen) and using three human colorectal carcinoma cell lines, LS-174T, WiDr and HT-29, as targets. A significant increase in ADCC activity was observed after PMNC were preincubated in 100-400 U/ml but not in lower concentrations of hrIL-6. Variations in activities of PMNC among donors were observed. Non-specific mAb showed no effect in augmenting ADCC activity. hrIL-6 treatment did not augment non-specific (non-mAb-mediated) cytotoxicity. The enhancement of ADCC activity was blocked by the addition of an antibody against hrIL-6 but not by an antibody to the IL-2 receptor (capable of blocking the induction of lymphokine-activated killer cell cytotoxicity by IL-2), suggesting that hrIL-6 augmentation of ADCC activity may not be mediated through IL-2. These results demonstrate that hrIL-6 augments ADCC activity of human PMNC using mAbs to human tumor antigens and human tumor cells as targets, suggesting a potential role for IL-6 in combination with anti-cancer antibodies for cancer immunotherapy.

MeSH terms

  • Adult
  • Antibodies, Monoclonal / immunology
  • Antibody-Dependent Cell Cytotoxicity / drug effects*
  • Antigens, Differentiation / analysis
  • Colorectal Neoplasms / immunology*
  • Colorectal Neoplasms / pathology
  • Dose-Response Relationship, Drug
  • Flow Cytometry
  • Humans
  • Interleukin-2 / pharmacology
  • Interleukin-6 / immunology
  • Interleukin-6 / pharmacology*
  • Killer Cells, Lymphokine-Activated / immunology
  • Leukocytes, Mononuclear / immunology*
  • Receptors, Fc / analysis
  • Receptors, IgG
  • Receptors, Interleukin-2 / immunology
  • Recombinant Proteins / pharmacology

Substances

  • Antibodies, Monoclonal
  • Antigens, Differentiation
  • Interleukin-2
  • Interleukin-6
  • Receptors, Fc
  • Receptors, IgG
  • Receptors, Interleukin-2
  • Recombinant Proteins