The aim of this study is to determine some functions of neutrophil in
patients affected by psoriatic arthritis and to compare them to those
of patients affected by cutaneous psoriasis and to normal controls. We
used a model of experimental cutaneous inflammation allowing to separ
ate a cluster of purified and viable PMN cells, Then we analyzed, with
in the three groups, the IL-8 concentration in serum and in the supern
atant obtained from the inflammatory site to gather data on the possib
le pathogenic role played by this cytokine in psoriatic arthritis. We
studied neutrophil functions in patients with cutaneous psoriasis and
psoriatic arthritis, in acute phase, in comparison with healthy contro
l subjects. We investigated in vivo neutrophil migration by Senn's ski
n window technique and measured adhesion assay and superoxide producti
on in circulating and migrating neutrophils after different stimuli. W
e also measured IL-8 concentration in serum and in the supernatant obt
ained from the inflammatory site, artificially created through the ski
n window scrape. Neutrophil migration in vivo was significantly higher
in both groups of patients than in controls. In the presence of fMLP,
blood cells showed a burst of superoxide release, which was significa
ntly more pronounced in patients when compared to healthy controls. Ne
utrophils from skin window scrape showed a much higher response to fML
P as compared to blood cells of all subject groups, but no differences
were observed between patients and controls. No correlation was found
between the three groups in adhesion ability under basal condition or
in response to different stimuli by circulating and migrating neutrop
hils. Our results also show a great increase of IL-8 in the exudate fr
om patients compared to controls. Our study shows that there is no dif
ference in neutrophil functions between patients with psoriatic arthri
tis and cutaneous psoriasis; moreover we suggest that the source of hi
gh IL-8 levels are neutrophils rather than the keratinocytes.