Cytokine production in patients with mite-sensitive bronchial asthma

Int Arch Allergy Immunol. 1994;104 Suppl 1(1):46-8. doi: 10.1159/000236750.

Abstract

We examined the eosinophil viability-enhancing activity (EVEA) of peripheral blood mononuclear cells (PBMNCs) obtained from mite-sensitive bronchial asthma (BA) and normal control subjects. Mite concentrations of 1 and 10 micrograms/ml significantly increased EVEA in BA patients as compared with normal controls (p < 0.05 and p < 0.05, respectively). The level of IFN-gamma in PBMNC culture supernatants was higher in BA patients than in normal controls. Dexamethasone, cyclosporin A and FK506 significantly inhibited EVEA in BA patients (p < 0.05 to p < 0.001).

MeSH terms

  • Allergens / adverse effects*
  • Animals
  • Antibodies / pharmacology
  • Asthma / immunology*
  • Asthma / metabolism
  • Cell Survival / drug effects
  • Cell Survival / immunology
  • Cyclosporine / pharmacology
  • Cytokines / biosynthesis*
  • Dexamethasone / pharmacology
  • Eosinophils / cytology
  • Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis
  • Granulocyte-Macrophage Colony-Stimulating Factor / immunology
  • Humans
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / immunology
  • Interleukin-3 / biosynthesis
  • Interleukin-3 / immunology
  • Interleukin-5 / biosynthesis
  • Interleukin-5 / immunology
  • Mites / immunology*
  • Tacrolimus / pharmacology

Substances

  • Allergens
  • Antibodies
  • Cytokines
  • Interleukin-3
  • Interleukin-5
  • Dexamethasone
  • Interferon-gamma
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Cyclosporine
  • Tacrolimus