In vivo CD30 expression in human diseases with predominant activation of Th2-like T cells

J Leukoc Biol. 1997 May;61(5):539-44.

Abstract

CD30 is a member of the tumor necrosis factor (TNF) receptor family, originally described as a marker for Hodgkin and Reed-Sternberg cells in Hodgkin's disease, which has been found to be preferentially expressed by T cells producing Th2-type cytokines. The presence of CD30 expression was assessed by both immunohistochemistry and reverse transcriptase-polymerase chain reaction in the target organs of patients with Th1- or Th2-dominated disorders. CD30 expression was found in neither the gut of patients with Crohn's disease nor in the gastric antrum of Helicobacter pylori-infected patients, where there was high interferon-gamma (IFN-gamma) expression. In contrast, high CD30 expression in the apparent absence of IFN-gamma expression was observed in the skin of patients with systemic sclerosis or chronic graft versus host disease (GVHD), which can be considered Th2-dominated disorders. Moreover, high levels of soluble CD30 were found in the serum of both systemic sclerosis and GVHD patients but not in the serum of patients suffering from multiple sclerosis, a Th1-dominated disorder. Thus, CD30 expression appears to be preferentially associated with Th2-type responses not only in vitro but also in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crohn Disease / blood
  • Crohn Disease / immunology
  • Crohn Disease / metabolism
  • Gastritis / blood
  • Gastritis / immunology
  • Gastritis / metabolism
  • Graft vs Host Disease / blood
  • Graft vs Host Disease / immunology
  • Graft vs Host Disease / metabolism
  • Humans
  • Immunohistochemistry
  • Ki-1 Antigen / biosynthesis*
  • Ki-1 Antigen / blood
  • Lymphocyte Activation / physiology*
  • Multiple Sclerosis / blood
  • Multiple Sclerosis / immunology
  • Multiple Sclerosis / metabolism
  • Scleroderma, Systemic / blood
  • Scleroderma, Systemic / immunology
  • Scleroderma, Systemic / metabolism
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Th2 Cells / immunology*
  • Th2 Cells / metabolism

Substances

  • Ki-1 Antigen