JP-8 jet fuel exposure rapidly induces high levels of IL-10 and PGE2 secretion and is correlated with loss of immune function

Toxicol Ind Health. 2007 May;23(4):223-30. doi: 10.1177/0748233707083956.

Abstract

The US Air Force has implemented the widespread use of JP-8 jet fuel in its operations, although a thorough understanding of its potential effects upon exposed personnel is unclear. Previous work has demonstrated that JP-8 exposure is immunosuppressive. In the present study, the potential mechanisms for the effects of JP-8 exposure on the immune system were investigated. Exposure of mice to JP-8 for 1 h/day resulted in immediate secretion of two immunosuppressive agents; namely, interleukin-10 (IL-10) and prostaglandin E2 (PGE2). JP-8 exposure rapidly induced a persistently high level of serum IL-10 and PGE2 at an exposure concentration of 1000 mg/m3. IL-10 levels peaked at 2 h post-JP-8 exposure and then stabilized at significantly elevated serum levels, while PGE2 levels peaked after 2-3 days of exposure and then stabilized. Elevated IL-10 and PGE2 levels may at least partially explain the effects of JP-8 exposure on immune function. Elevated IL-10 and PGE2 levels, however, cannot explain all of the effects due to JP-8 exposure (e.g., decreased organ weights and decreased viable immune cells), as treatment with a PGE2 inhibitor did not completely reverse the immunosuppressive effects of jet fuel exposure. Thus, low concentration JP-8 jet fuel exposures have significant effects on the immune system, which can be partially explained by the secretion of immunosuppressive modulators, which are cumulative over time.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Celecoxib
  • Cyclooxygenase Inhibitors / pharmacology
  • Dinoprostone / blood*
  • Dinoprostone / metabolism
  • Female
  • Hydrocarbons / toxicity*
  • Inhalation Exposure / adverse effects
  • Interleukin-10 / blood*
  • Interleukin-10 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Models, Animal
  • Pyrazoles / pharmacology
  • Sulfonamides / pharmacology
  • Teratogens / toxicity*
  • Time Factors

Substances

  • Cyclooxygenase Inhibitors
  • Hydrocarbons
  • JP8 aviation fuel
  • Pyrazoles
  • Sulfonamides
  • Teratogens
  • Interleukin-10
  • Celecoxib
  • Dinoprostone