Interleukin 10 inhibits cytokine production of human AML cells

Ann Oncol. 1996 Apr;7(4):397-404. doi: 10.1093/oxfordjournals.annonc.a010607.

Abstract

Background: Unlike normal hematopoietic cells leukemic blasts from patients with AML constitutively express cytokines like IL1, GM-CSF and TNF alpha and it has been suggested that these cytokines may regulate growth and differentiation of the malignant cells. IL10 inhibits cytokine production of activated macrophages and T-helper 1 cells. We analysed whether IL10 can also suppress cytokine production and may inhibit growth of AML cells.

Materials and methods: AML blasts of 18 patients were purified by immunomagnetic separation and cultured in serum-free medium in the presence of cytokines. The production of cytokines was analysed by ELISA, DNA synthesis by 3H-thymidine incorporation and mRNA expression of cytokine genes by semiquantitative RT-PCR.

Results: Our results confirm previous results that AML blasts produce a variety of cytokines such as GM-CSF, IL1 alpha, IL1 beta, IL6 and TNF alpha. AML cells were induced to proliferation by G-CSF, GM-CSF, IL3, IL1 beta and SCF to a different extent. In contrast, IL10 significantly inhibited the cytokine production at the mRNA and protein level and spontaneous thymidine uptake in a dose-dependent way. This inhibition could be abrogated by IL10 specific antibodies.

Conclusion: These observations suggest an inhibitory effect of IL10 on the proliferation of cultured AML blasts most likely through suppression of endogenous cytokines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Aged
  • Antibodies, Monoclonal
  • Cell Division / drug effects
  • Cytokines / biosynthesis*
  • Cytokines / metabolism
  • DNA, Neoplasm / biosynthesis
  • Female
  • Granulocyte-Macrophage Colony-Stimulating Factor / genetics
  • Humans
  • Interleukin-10 / immunology
  • Interleukin-10 / pharmacology*
  • Leukemia, Myeloid / drug therapy*
  • Leukemia, Myeloid / metabolism
  • Leukemia, Myeloid / physiopathology
  • Male
  • Middle Aged
  • RNA, Messenger / biosynthesis
  • RNA, Neoplasm / biosynthesis
  • Stimulation, Chemical
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Antibodies, Monoclonal
  • Cytokines
  • DNA, Neoplasm
  • RNA, Messenger
  • RNA, Neoplasm
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Granulocyte-Macrophage Colony-Stimulating Factor