IL-10 contributes to the inhibition of contact hypersensitivity in mice treated with photodynamic therapy

J Immunol. 2000 Mar 1;164(5):2457-62. doi: 10.4049/jimmunol.164.5.2457.

Abstract

We have explored the effect of photodynamic therapy (PDT) with verteporfin on the induction and expression of contact hypersensitivity (CHS) to 2,4-dinitrofluorobenzene (DNFB) in normal mice and IL-10-deficient mice. Our results indicate that DNFB sensitized mice given PDT with verteporfin and whole body red light irradiation exhibited a significant reduction in CHS compared with control animals. Administration of rIL-12 reversed the effect(s) of PDT as did treatment of mice with anti-IL-10-neutralizing Ab. Knockout mice deficient in IL-10 were found to be resistant to the inhibitory effects of PDT. In vitro proliferative responses using spleen cells from DNFB-sensitized and PDT-treated mice showed a significantly lower response to DNBS as compared with cells from DNFB-sensitized mice or DNFB and PDT-treated IL-10-deficient mice. Finally, naive mice exposed to PDT exhibited an increase in skin IL-10 levels, which peaked between 72 and 120 h post-PDT. Together these data support the role of IL-10 as a key modulator in the inhibition of the CHS response by whole body PDT.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • Dermatitis, Contact / drug therapy
  • Dermatitis, Contact / genetics
  • Dermatitis, Contact / immunology*
  • Dermatitis, Contact / prevention & control*
  • Dinitrofluorobenzene / immunology
  • Ear, External / immunology
  • Female
  • Interleukin-10 / biosynthesis
  • Interleukin-10 / genetics
  • Interleukin-10 / immunology
  • Interleukin-10 / physiology*
  • Lymphocyte Activation / drug effects
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Photochemotherapy* / methods
  • Skin / immunology
  • Skin / metabolism
  • Spleen / cytology
  • Spleen / drug effects
  • Spleen / immunology

Substances

  • Antibodies, Monoclonal
  • Interleukin-10
  • Dinitrofluorobenzene