Vitamin E-loaded dialyzer resets PBMC-operated cytokine network in dialysis patients

Kidney Int. 2004 Apr;65(4):1473-81. doi: 10.1111/j.1523-1755.2004.00528.x.

Abstract

Background: In hemodialysis patients the activity of stimulated Th1 lymphocytes is depressed, while Th2 cells are constitutively primed. Such phenomena may depend on monocyte activation and altered release of interleukin (IL)-12 and IL-18, which regulate Th cell differentiation. Reactive oxygen species (ROS) activate monocytes; therefore, a hemodialyzer with antioxidant activity would contrast ROS, prevent monocyte activation, reset IL-12 and IL-18 release, and restore Th1/Th2 balance.

Methods: Ten patients on regular dialysis treatment (RDT) with cellulosic membrane (CM) were shifted to vitamin E-coated dialyzer (VE). During treatment with CM and after 3, 6, and 12 months of treatment with VE, peripheral blood mononuclear cells (PBMC) and purified CD4+ cells were isolated, and cultured, resting, mitogen-stimulated, and interferon gamma (IFNgamma), IL-4, IL-10, IL-12, and IL-18 release was measured. Vitamin E and A plasma levels and the effects of a single dialysis session on peripheral blood NO levels were assayed.

Results: The constitutive release of IL-4 and IL-10 by CD4+ cells was abated significantly by treatment with VE (nadir -77.8% and -55.3%, respectively, at 12 months). INFgamma release by mitogen-stimulated CD4+ recovered with VE (zenith +501% at 12 months). PBMC constitutive production of IL-12 and IL-18 was significantly reduced by VE (nadir at 12 months -64.7% and -51.3%, respectively). VE increased plasma levels of vitamins E and A. NO plasma levels fell after a single dialysis treatment with VE (-17%, P < 0.05) in contrast with CU (+27.1%, P < 0.05).

Conclusion: The network of cytokines released by monocytes and Th cells is reset toward normality by treatment with vitamin E-coated dialyzer.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Adult
  • Antioxidants* / metabolism
  • Biocompatible Materials
  • CD4-Positive T-Lymphocytes / drug effects
  • CD4-Positive T-Lymphocytes / metabolism
  • Cells, Cultured
  • Cellulose / analogs & derivatives*
  • Coated Materials, Biocompatible*
  • Cytokines / blood*
  • Female
  • Humans
  • Interferon-gamma / metabolism
  • Interleukins / metabolism
  • Male
  • Membranes, Artificial*
  • Middle Aged
  • Monocytes / drug effects
  • Monocytes / metabolism*
  • Nitric Oxide / blood
  • Renal Dialysis / instrumentation*
  • Retreatment
  • Time Factors
  • Vitamin A / blood
  • Vitamin E* / blood

Substances

  • Antioxidants
  • Biocompatible Materials
  • Coated Materials, Biocompatible
  • Cytokines
  • Interleukins
  • Membranes, Artificial
  • Vitamin A
  • Vitamin E
  • Nitric Oxide
  • acetylcellulose
  • Interferon-gamma
  • Cellulose