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The response to ultraviolet radiation and delayed hypersensitivity in Celts with skin cancer
Author(s) -
Long C.C.,
Marks R.
Publication year - 1996
Publication title -
journal of the european academy of dermatology and venereology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 107
eISSN - 1468-3083
pISSN - 0926-9959
DOI - 10.1111/j.1468-3083.1996.tb00128.x
Subject(s) - erythema , medicine , skin cancer , epidermis (zoology) , dermatology , delayed hypersensitivity , photodermatosis , pathology , immunology , immune system , cancer , biology , dna damage , genetics , anatomy , dna , xeroderma pigmentosum
Background The reasons for the apparent increased risk of skin cancer in Celts are unclear, but it is possible that Celts possess more risk factors than non‐Celts. Aims To determine whether Celts differ from non‐Celts with respect of cutaneous response to UVR, and tests of cell mediated immunity. Methods The MED of UVB, degree of clinical photodamage, pigmentation, numbers of peripheral blood T‐lymphocyte sub‐sets, and response to a battery of infra‐dermal antigens were determined in 18 Celts with a history of BCC and 18 age, sex, and skin type matched non‐Celts with a history of BCC. Each was then exposed to 2MED, and biopsies taken of irradiated and non‐irradiated sites at 24 h. Results Celts tended to have a thinner epidermis than the non‐Celts. Following irradiation the epidermal thymidine labelling index in Celts had almost doubled, whereas in non‐Celts it fell slightly. We found no differences in photodamage, freckling, pigmentation, MED, the erythema response to 2MED, numbers of peripheral T‐lymphocytes, or tests of cell mediated immunity. Summary The tendency of Celts to a thinner epidermis and an increased epidermal labelling index following UV irradiation may be a reflection of an increased susceptibility to skin damage following UV exposure.