Related Experiment Videos
Ultraviolet radiation causes less immunosuppression in patients with polymorphic light eruption than in controls
Roy A Palmer1, Peter S Friedmann
1Department of Dermatopharmacology, Southampton General Hospital, Southampton, UK. roypalmer@totalise.co.uk
The Journal of Investigative Dermatology
|March 11, 2004
Summary
Polymorphic light eruption (PLE) patients show reduced UVR-induced immunosuppression, leading to a stronger sensitization response to 2,4-dinitrochlorobenzene after UVR exposure compared to controls. This suggests a partial failure in UVR-induced immune suppression in PLE.
Area of Science:
- Immunology
- Dermatology
- Photobiology
Background:
- Polymorphic light eruption (PLE) is a common photodermatosis.
- It is hypothesized that PLE involves impaired ultraviolet radiation (UVR)-induced immunosuppression.
- This impairment may lead to delayed-type hypersensitivity to photo-induced antigens.
Purpose of the Study:
- To investigate the susceptibility of PLE patients to UVR-induced immunosuppression.
- To compare the immune response to 2,4-dinitrochlorobenzene (DNCB) after UVR exposure in PLE patients and controls.
- To assess the immune response to diphenylcyclopropenone (DPCP) without UVR exposure in both groups.
Main Methods:
- Thirteen PLE patients and 11 controls were exposed to 1 minimum erythema dose (MED) of UVR.
- Sensitization with 2,4-dinitrochlorobenzene (DNCB) was performed on UVR-exposed skin, and with diphenylcyclopropenone (DPCP) on non-irradiated skin.
- Reactivity was measured by skin thickness increase after challenge doses of DNCB and DPCP.
Main Results:
- A strong correlation was observed between reactivity to DNCB and DPCP across all subjects.
- The reaction to DNCB relative to DPCP was significantly greater in PLE patients than in controls.
- This indicates that UVR suppressed DNCB sensitization less in PLE patients.
Conclusions:
- Patients with polymorphic light eruption exhibit a partial failure of UVR-induced immunosuppression.
- The induction of sensitization by 2,4-dinitrochlorobenzene is less suppressed by UVR in PLE patients compared to healthy individuals.
- This finding supports the hypothesis that impaired UVR-induced immunosuppression plays a role in the pathogenesis of PLE.