DIFFERENTIAL-EFFECTS OF A MONOCLONAL-ANTIBODY TO CIS-UROCANIC ACID ONTHE SUPPRESSION OF DELAYED AND CONTACT HYPERSENSITIVITY FOLLOWING ULTRAVIOLET-IRRADIATION
Am. Moodycliffe et al., DIFFERENTIAL-EFFECTS OF A MONOCLONAL-ANTIBODY TO CIS-UROCANIC ACID ONTHE SUPPRESSION OF DELAYED AND CONTACT HYPERSENSITIVITY FOLLOWING ULTRAVIOLET-IRRADIATION, The Journal of immunology, 157(7), 1996, pp. 2891-2899
Urocanic acid (UCA) occurs naturally in the stratum corneum of the ski
n as the transisomer and, upon exposure to UVB radiation, converts to
cis-UCA. It has been proposed that trans-UCA is the photoreceptor for
and, following its isomerization to cis-UCA, a mediator of the suppres
sive effects of UVB irradiation on systemic T cell-mediated immune res
ponses, such as contact hypersensitivity (CH) and delayed-type hyperse
nsitivity (DTH). To address this question directly, we studied the con
sequence of deleting the in vivo function of cis-UCA on systemic suppr
ession of CH and DTH, by injecting mice with a anti-cis-UCA mAb severa
l hours before exposure to UVB radiation. We found that while DTH resp
onses were completely restored, the anti-cis-UCA Ab had no effect on U
V-induced immunosuppression of the CH response, even though suppressor
cell formation was inhibited in both cases. Further, the kinetics of
IL-10 expression in the skin of irradiated mice injected with the anti
-cis-UCA mAb was altered and the diminished APC function of spleen-adh
erent cells from UVB-irradiated mice was totally reversed by the Ab. T
hese findings suggest that cis-UCA acts as a mediator for some but not
all of the systemic suppressive effects of UVB irradiation. They also
suggest that cis-UCA may act indirectly via IL-10 to modulate immune
function.