Perilymphatic injections of recombinant interleukin-2 (rIL-2) partially correct the immunologic defects in patients with advanced head and neck squamous cell carcinoma

Laryngoscope. 1992 May;102(5):572-8. doi: 10.1288/00005537-199205000-00018.

Abstract

Patients with advanced head and neck squamous cell carcinoma (HNSCC) are severely immunocompromised. In virtually all such patients who have been studied, reduced numbers of circulating CD3+ T-cell-receptor (TCR)alpha/beta+ T lymphocytes, a reduction of natural killer (NK) activity, and a poor induction of lymphokine-activated killer (LAK) cell activity (following in vitro treatment with recombinant interleukin-2 [rIL-2]) have been detected. Recently, however, it has been demonstrated that perilymphatic injections of low doses of rIL-2 may induce a local reduction of tumor masses in these patients. The present study, a cooperative pilot effort on the clinical effects of this route of administration, showed an activation of the lytic machinery in lymphocytes belonging to the T-cell lineage, as well as a potentiation of NK activity in the peripheral blood. These findings demonstrated that the severe immunodeficiency of HNSCC patients may be at least partially corrected by in vivo administration of rIL-2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antigens, Surface / analysis
  • Carcinoma, Squamous Cell / immunology*
  • Carcinoma, Squamous Cell / therapy
  • Female
  • Head and Neck Neoplasms / immunology*
  • Head and Neck Neoplasms / therapy
  • Humans
  • Immunocompromised Host / immunology*
  • Injections, Intralymphatic
  • Interleukin-2 / administration & dosage
  • Interleukin-2 / therapeutic use*
  • Killer Cells, Lymphokine-Activated / immunology
  • Killer Cells, Lymphokine-Activated / pathology
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / pathology
  • Leukocyte Count
  • Male
  • Middle Aged
  • Perilymph
  • Phenotype
  • Recombinant Proteins
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / pathology
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Helper-Inducer / pathology

Substances

  • Antigens, Surface
  • Interleukin-2
  • Recombinant Proteins