Monokine antagonism is reduced in patients with IDDM

Diabetes. 1994 Oct;43(10):1242-7. doi: 10.2337/diab.43.10.1242.

Abstract

Interleukin-1 (IL-1) and tumor necrosis factor alpha (TNF-alpha) have been implicated as immune effector molecules in the pathogenesis of insulin-dependent diabetes mellitus (IDDM). Recently, an increased frequency of the A1/A1 genotype of an IL-1 receptor antagonist (IL-1Ra) gene polymorphism was observed in patients with IDDM. Therefore, we investigated plasma IL-1Ra and soluble TNF p55 receptor (TNFsRp55) levels in 18 men with recent-onset IDDM, 10 men with long-standing IDDM, and 35 age-matched healthy men. No differences in plasma IL-1Ra were found among the three groups. However, when the plasma IL-1Ra levels in the subjects with IDDM and the control subjects were analyzed according to IL-1Ra genotypes, we found a 30% lower level of plasma IL-1Ra in subjects with IDDM carrying the A1/A1 genotype compared with the levels in those carrying the A1/A2 genotype (372 +/- 40 vs. 530 +/- 54 ng/l, respectively, P = 0.025). In contrast, no significant association was seen between plasma IL-1Ra and IL-1Ra genotype in the control subjects. The TNFsRp55 level in heparinized plasma was 17% lower in patients with IDDM than in control subjects (3.93 +/- 0.22 vs. 4.72 +/- 0.24 micrograms/l, respectively, P = 0.038). These findings could not be explained by metabolic derangement in the IDDM patients.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Base Sequence
  • Blood Glucose / metabolism
  • DNA Primers
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / genetics*
  • Diabetes Mellitus, Type 1 / immunology*
  • Genotype
  • Humans
  • Interleukin 1 Receptor Antagonist Protein
  • Leukocyte Count
  • Male
  • Molecular Sequence Data
  • Monokines / antagonists & inhibitors*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*
  • Radioimmunoassay
  • Receptors, Tumor Necrosis Factor / analysis*
  • Reference Values
  • Sialoglycoproteins / biosynthesis
  • Sialoglycoproteins / blood*
  • Sialoglycoproteins / genetics

Substances

  • Blood Glucose
  • DNA Primers
  • IL1RN protein, human
  • Interleukin 1 Receptor Antagonist Protein
  • Monokines
  • Receptors, Tumor Necrosis Factor
  • Sialoglycoproteins