ULTRAVIOLET-B INDUCED SUPPRESSION OF INDUCTION OF CONTACT SENSITIVITYIN HUMAN SKIN IS NOT ASSOCIATED WITH TUMOR NECROSIS FACTOR-ALPHA-308 OR INTERLEUKIN-10 GENETIC POLYMORPHISMS
Mh. Allen et al., ULTRAVIOLET-B INDUCED SUPPRESSION OF INDUCTION OF CONTACT SENSITIVITYIN HUMAN SKIN IS NOT ASSOCIATED WITH TUMOR NECROSIS FACTOR-ALPHA-308 OR INTERLEUKIN-10 GENETIC POLYMORPHISMS, British journal of dermatology, 139(2), 1998, pp. 225-229
Low doses of ultraviolet B (UVB) can induce localized immunosuppressio
n in skin. This effect may be important in the induction of skin cance
rs and is thought to be mediated by tumour necrosis factor (TNF) (alph
a and interleukin (IL) 10 iii conjunction with other factors. In human
s a transition polymorphism in the TNF-alpha gene may affect TNF-alpha
secretion and the promoter region of the IL-10 gene contains a CA rep
eat polymorphism which may affect gene function. We have therefore inv
estigated the association of these polymorphisms with WE-induced immun
osuppression in humans. Volunteers (n=42) were irradiated with UVB the
n sensitized on irradiated skin with diphenylcyclopropanone (DPCP) and
subsequently antigen challenged with DPCP, DNA was extracted from blo
od samples and volunteers genotyped for the TNF-alpha polymorphism by
polymerase chain reaction (PCR) and restriction digestion, The CA repe
at polymorphism was amplified by PCR and sized by gel electrophoresis.
Twenty-four volunteers were susceptible to UVB-induced immunosuppress
ion and 18 were resistant, The association of allele frequencies and p
henotype was statistically tested using a chi(2)-test, For both the TN
F-alpha and IL-10 polymorphisms, there was no statistically significan
t association between allele types and response to UVB. These results
indicate that variation in the immune response to UVB in humans is not
associated with the TNF-alpha-308 transition or IL-10 CA repeat polym
orphisms, although other as yet undetected DNA sequence variants of th
ese genes may be involved.