EPIDERMAL-CELL DNA CONTENT AND INTERMEDIATE FILAMENTS KERATIN-10 AND VIMENTIN AFTER TREATMENT OF PSORIASIS WITH CALCIPOTRIOL CREAM ONCE-DAILY, TWICE-DAILY AND IN COMBINATION WITH CLOBETASONE 17-BUTYRATE CREAM OR BETAMETHASONE 17-VALERATE CREAM - A COMPARATIVE FLOW CYTOMETRIC STUDY
Cp. Glade et al., EPIDERMAL-CELL DNA CONTENT AND INTERMEDIATE FILAMENTS KERATIN-10 AND VIMENTIN AFTER TREATMENT OF PSORIASIS WITH CALCIPOTRIOL CREAM ONCE-DAILY, TWICE-DAILY AND IN COMBINATION WITH CLOBETASONE 17-BUTYRATE CREAM OR BETAMETHASONE 17-VALERATE CREAM - A COMPARATIVE FLOW CYTOMETRIC STUDY, British journal of dermatology, 135(3), 1996, pp. 379-384
Calcipotriol and corticosteroids, two therapy modalities frequently pr
escribed in the treatment of psoriasis, are often used in combination.
The aim of the present study was to determine whether the cell biolog
ical response pattern of concurrent use of calcipotriol and corticoste
roids is different from calcipotriol monotherapy, Forty patients with
chronic plaque psoriasis were divided at random in four parallel group
s and treated for 8 weeks with: (1) calcipotriol cream (50 mu g/g once
daily); (2) calcipotriol cream twice daily; (3) calcipotriol and clob
etasone 17-butyrate (0.5 mg/g) creams; and (4) calcipotriol and betame
thasone 17-valerate (1 mg/g) creams, Before and after treatment kerato
tome biopsies were taken and single cell suspensions prepared for now
cytometric analysis, Flow cytometric multiparameter quantification of
markers for proliferation (TO-PRO-3), differentiation (antikeratin 10)
and inflammation (antivimentin) was used to evaluate all four therapy
modalities. A statistically significant decrease of the percentage of
basal cells in S- and G(2)M-phase (proliferation) was obtained with a
ll therapy modalities, except for calcipotriol monotherapy applied onc
e daily. A significant reduction of the number of vimentin-positive ce
lls (non-keratinocytes) was observed following combined treatment with
calcipotriol acid clobetasone butyrate. In contrast, monotherapy with
calcipotriol had virtually no effect on the number of vimentin-positi
ve cells. It can be concluded that: (i) calcipotriol monotherapy, appl
ied once daily was less antiproliferative compared with twice daily ap
plications of calcipotriol or the combined treatment with corticostero
ids and that (ii) the combination of calcipotriol and corticosteroids
proved to have a marked effect on the percentage of non-keratinocytes,
in contrast to the modest effect of calcipotriol.