Enhanced monocyte Th1 cytokine production in HCV-infected cryoglobulinemic patients

J Hepatol. 2003 Feb;38(2):230-6. doi: 10.1016/s0168-8278(02)00353-7.

Abstract

Background/aims: The etiologic link between chronic hepatitis C virus (HCV) infection and mixed cryoglobulinemia is well established, while its prognostic significance within the context of HCV-related hepatitis is not as clear. Patients with an HCV-related cryoglobulinemic syndrome oft have mild liver disease, an aspect that can be influenced by an individual's Th1/Th2 orientation. Our goal was to document stigmata of differentiate cytokine production in this subgroup of patients.

Methods: Fifteen patients with chronic HCV-related liver disease (CLD) and a cryoglobulinemic syndrome (CRYO) were compared to age/sex matched CLD controls with negative cryocrit. Cultured monocytes were stimulated with either Staphylococcus aureus (SAC) or lipopolysaccharide (LPS).

Results: The protein concentrations of TNF-alpha and of the Th1-type cytokines interleukin (IL)-12 and IL-18 were significantly greater in the CRYO group, while IL-10 (a Th2 cytokine) levels were greater in the control group.

Conclusions: The clinical distinctiveness of the two groups was reflected at the cytokine level. The cryoglobulinemic patients studied showed a greater Th1 polarization than their cryoglobulin-negative counterparts. This enhanced production of Th1-type cytokines is seemingly not able to rid the host of infection but may account for a milder course of liver disease.

MeSH terms

  • Adult
  • Aged
  • Cells, Cultured
  • Cryoglobulinemia / etiology
  • Cryoglobulinemia / immunology*
  • Cytokines / metabolism*
  • Female
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / immunology*
  • Humans
  • Interleukin-10 / metabolism
  • Interleukin-12 / metabolism
  • Interleukin-18 / metabolism
  • Lipopolysaccharides / pharmacology
  • Male
  • Middle Aged
  • Monocytes / cytology
  • Monocytes / metabolism*
  • Monocytes / virology
  • Staphylococcus aureus
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Interleukin-18
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Interleukin-12