The in vivo biologic effect of interleukin 2 and interferon alfa on natural immunity in patients with head and neck cancer

Arch Otolaryngol Head Neck Surg. 1990 Nov;116(11):1302-8. doi: 10.1001/archotol.1990.01870110074009.

Abstract

Given the association of deficient natural immunity with the risk of metastatic disease, the ability to activate natural killer cell function may have a therapeutic significance. The effect of continuous infusion of interleukin 2 plus intramuscular interferon alfa on natural immune status was, therefore, analyzed in eight patients with head and neck cancer. Also evaluated was the effect of interleukin 2-interferon alfa therapy on lymphokine-activated killer cell activity as well as total lymphocyte count, percent of lymphocyte subsets, and levels of both circulating immune complexes and antibody classes. Both the percent and absolute number of natural killer cells (ie, CD56+ CD3- lymphocytes) within peripheral blood as well as natural killer cell activity against K562 targets increased significantly with treatment. The remaining immune parameters were not significantly altered. The demonstrated capacity to modulate natural immune function supports the potential use of interleukin 2-containing regimens as a preventive measure against metastatic disease in patients with head and neck cancer.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Antigen-Antibody Complex / analysis
  • Drug Therapy, Combination
  • Female
  • Head and Neck Neoplasms / immunology*
  • Head and Neck Neoplasms / therapy
  • Humans
  • Immunity, Innate / drug effects
  • Injections, Intramuscular
  • Interferon Type I / administration & dosage
  • Interferon Type I / therapeutic use*
  • Interleukin-2 / therapeutic use*
  • Killer Cells, Lymphokine-Activated / drug effects
  • Killer Cells, Natural / drug effects
  • Lymphocytes / immunology
  • Male
  • Middle Aged
  • Neoplasm Metastasis / prevention & control

Substances

  • Antigen-Antibody Complex
  • Interferon Type I
  • Interleukin-2