Prevention of UV radiation-induced immunosuppression by IL-12 is dependent on DNA repair

J Exp Med. 2005 Jan 17;201(2):173-9. doi: 10.1084/jem.20041212.

Abstract

The immunostimulatory cytokine IL-12 is able to antagonize immunosuppression induced by solar/ultraviolet (UV) radiation via yet unknown mechanisms. IL-12 was recently found to induce deoxyribonucleic acid (DNA) repair. UV-induced DNA damage is an important molecular trigger for UV-mediated immunosuppression. Thus, we initiated studies into immune restoration by IL-12 to discern whether its effects are linked to DNA repair. IL-12 prevented both UV-induced suppression of the induction of contact hypersensitivity and the depletion of Langerhans cells, the primary APC of the skin, in wild-type but not in DNA repair-deficient mice. IL-12 did not prevent the development of UV-induced regulatory T cells in DNA repair-deficient mice. In contrast, IL-12 was able to break established UV-induced tolerance and inhibited the activity of regulatory T cells independent of DNA repair. These data identify a new mechanism by which IL-12 can restore immune responses and also demonstrate a link between DNA repair and the prevention of UV-induced immunosuppression by IL-12.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / pharmacology*
  • Animals
  • Antigen-Presenting Cells / drug effects
  • DNA Damage / physiology
  • DNA Repair / physiology*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Immune System / drug effects*
  • Immune System / radiation effects*
  • Immunosuppression Therapy*
  • Interleukin-12 / pharmacology*
  • Langerhans Cells / drug effects
  • Langerhans Cells / radiation effects
  • Mice
  • Ultraviolet Rays
  • Xeroderma Pigmentosum Group A Protein

Substances

  • Adjuvants, Immunologic
  • DNA-Binding Proteins
  • Xeroderma Pigmentosum Group A Protein
  • Xpa protein, mouse
  • Interleukin-12