Evaluation of cases with silicosis using the parameters related to Fas-mediated apoptosis

Int J Mol Med. 1999 Oct;4(4):407-11. doi: 10.3892/ijmm.4.4.407.

Abstract

To establish a new clinical index for immunological abnormalities occurring in silicosis, several clinical parameters related to Fas-mediated apoptosis; i.e., membrane Fas expression on peripheral blood lymphocytes (mFas), serum soluble Fas levels (sFas), serum soluble Fas ligand levels (sFasL), and soluble/membrane Fas mRNA expression ratios (s/mFas ExR) in peripheral blood mononuclear cells (PBMC) were investigated. Fifty-eight silicosis patients with no clinical symptoms of autoimmune diseases were the subjects of this study. Factor analysis was performed using 12 clinical parameters including four parameters related to Fas-mediated apoptosis. Two common factors were identified. Factor 1 which consisted of the following parameters; duration of exposure, symptomatic dyspnea, PO2, PCO2, and A-aDO2, should be designated as the respiratory factor for cases with silicosis. The parameters of factor 2 were serum IgG, sFas with high factor loading, titer of ANA, sFasL, and s/mFas ExR. These parameters of factor 2 are indicative of the immunological disorders occurring in silicosis cases. Some cases exhibited abnormalities in parameters of factor 2 but not factor 1. The factor analysis clearly demonstrated that the parameters related to Fas-mediated apoptosis should be the most beneficial for predicting the pre-clinical status of complicated autoimmune diseases in silicosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Apoptosis / immunology*
  • Fas Ligand Protein
  • Female
  • Humans
  • Lymphocytes / immunology
  • Lymphocytes / pathology
  • Male
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / blood
  • Membrane Glycoproteins / immunology*
  • RNA, Messenger / analysis
  • Silicosis / blood
  • Silicosis / immunology*
  • Silicosis / pathology
  • fas Receptor / biosynthesis
  • fas Receptor / blood
  • fas Receptor / immunology*

Substances

  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • RNA, Messenger
  • fas Receptor