Modulating effect of interleukin 2 therapy on interferon production by blood leukocytes of patients with minimal residual hematological disease

Arch Immunol Ther Exp (Warsz). 1997;45(2-3):177-81.

Abstract

This study was designed to investigate the effect of 1.8 x 10(6) U/day interleukin 2 (IL-2) therapy on interferon (IFN) production. Patients enrolled in the study suffered from multiple myeloma (MM), Hodgkin's disease (HD) and non-Hodgkin lymphoma (NHL). All of them were in remission after chemotherapy or radiotherapy. Results indicated that IL-2 given subcutaneously at a dose of 1.8 x 10(6) U/day for 3 weeks induced IFN-gamma in serum of patients and caused a prolonged effect on the ability of blood leukocytes to produce IFN-gamma after stimulation in vitro by mitogen phytohemagglutinin (PHA). Such enhancement of IFN-gamma production may be beneficial for antitumor immune response. Low-dose IL-2 therapy was well tolerated by all patients and side effects not exceeding II grade of toxicity according to WHO scale were observed. Five patients with MM have relapsed 3-10 months after cesation of IL-2 therapy but 15 patients 18 months after therapy were in complete remission.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Combined Modality Therapy
  • Drug Evaluation
  • Female
  • Hematologic Neoplasms / drug therapy
  • Hematologic Neoplasms / mortality
  • Hematologic Neoplasms / pathology
  • Hematologic Neoplasms / radiotherapy
  • Hematologic Neoplasms / therapy*
  • Humans
  • Immunologic Factors / adverse effects
  • Immunologic Factors / pharmacology
  • Immunologic Factors / therapeutic use*
  • Interferon-gamma / biosynthesis*
  • Interleukin-2 / adverse effects
  • Interleukin-2 / pharmacology
  • Interleukin-2 / therapeutic use*
  • Leukocytes / drug effects*
  • Leukocytes / metabolism
  • Male
  • Middle Aged
  • Neoplasm, Residual
  • Recombinant Proteins / adverse effects
  • Recombinant Proteins / pharmacology
  • Recombinant Proteins / therapeutic use
  • Remission Induction

Substances

  • Immunologic Factors
  • Interleukin-2
  • Recombinant Proteins
  • Interferon-gamma