Autoimmune potential of perchloroethylene: Role of lipid-derived aldehydes

Toxicol Appl Pharmacol. 2017 Oct 15;333:76-83. doi: 10.1016/j.taap.2017.08.009. Epub 2017 Aug 14.


Tetrachloroethene (perchloroethylene, PCE), an ubiquitous environmental contaminant, has been implicated in inducing autoimmunity/autoimmune diseases (ADs), including systemic lupus erythematosus (SLE) and scleroderma in humans. However, experimental evidence suggesting the potential of PCE in mediating autoimmunity is lacking. This study was, therefore, undertaken to explore PCE's potential in inducing/exacerbating an autoimmune response. Six-week old female MRL+/+ mice, in groups of 6 each, were treated with PCE (0.5mg/ml) via drinking water for 12, 18 and 24weeks and markers of autoimmunity and oxidative stress were evaluated. PCE exposure led to significant increases in serum anti-nuclear antibodies (ANA), anti-dsDNA and anti-scleroderma-70 (anti-Scl-70) antibodies at 18weeks and, to a greater extent at 24weeks, suggesting that PCE exposure exacerbated autoimmunity in our animal model. The increases in autoantibodies were associated with time-dependent increases in malondialdehyde (MDA)-protein adducts and their antibodies, as well as significantly decreased levels of antioxidants GSH and SOD. The splenocytes isolated from mice treated with PCE for 18 and 24weeks showed greater Th17 cell proliferation and increased release of IL-17 in culture supernatants following stimulation with MDA-mouse serum albumin adducts, suggesting that MDA-modified proteins may act as an immunologic trigger by activating Th17 cells and contribute to PCE-mediated autoimmunity. Our studies thus provide an experimental evidence that PCE induces/exacerbates an autoimmune response and lipid-derived aldehydes (such as MDA) contribute to this response.

Keywords: Autoantibody; Autoimmunity; Lipid-derived aldehydes; Oxidative stress; Perchloroethylene; Th17 cell.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antibodies / blood
  • Autoimmunity / drug effects*
  • Cell Proliferation / drug effects
  • Disease Models, Animal
  • Female
  • Glutathione / blood
  • Interleukin-17 / metabolism
  • Lipids
  • Lupus Erythematosus, Systemic
  • Malondialdehyde / metabolism*
  • Mice
  • Protein Binding
  • Scleroderma, Systemic
  • Solvents / toxicity*
  • Spleen / cytology
  • Superoxide Dismutase / blood
  • Tetrachloroethylene / toxicity*
  • Th17 Cells / drug effects


  • Antibodies
  • Interleukin-17
  • Lipids
  • Solvents
  • Malondialdehyde
  • Superoxide Dismutase
  • Glutathione
  • Tetrachloroethylene