Scalp Psoriasis Clinical Trial
Official title:
Role of Il-17a in Difficult to Treat Variants of Psoriasis Including Palmo-plantar Psoriasis
The goal of this project is to study some mechanisms involved in the dysregulation of the immune system observed in the skin of subjects with psoriasis. This will be done by analyzing specific immune cells as well as gene and protein expression in small skin samples (biopsies) from patients with psoriasis. These results will be compared to the skin of healthy subjects without psoriasis.
A total of 80 subjects with psoriasis not currently using systemic treatment, with at least
one psoriatic plaque on the trunk or proximal limbs and having also more resistant to treat
psoriasis areas will be recruited. These subjects will be classified in the following 5
groups according to the localization of resistant areas: scalp psoriasis (20 subjects),
pustular palmo-plantar psoriasis (10 subjects), non-pustular palmo-plantar psoriasis (10
subjects), elbow psoriasis (20 subjects) and lower leg psoriasis (20 subjects).
At Day 0 visit, severity of psoriasis will be evaluated using the body surface area (BSA)
and the Psoriasis Area and Severity Index (PASI).
After appropriate washout periods, all 80 subjects will have two skin biopsies: one from a
plaque located on the trunk or proximal limbs and one on a plaque located on an area more
resistant to treatment (scalp, palms/soles, elbow or lower leg). Each biopsy will be split
in half. One part will be used for a limited immunohistochemistry panel and additional
staining will be performed on samples from the pustular palmo-plantar psoriasis and
non-pustular palmo-plantar psoriasis subjects to localize IL-17A and IL-23 producing cells.
The other half will be used for gene expression analysis using
Reverse-Transcription-Polymerase Chain Reaction (RT-PCR) for all subjects including the
following genes: IL-23 (p40 & p19), IL-17A and Human Acidic Ribosomal Protein (HARP). In
addition, the expression of other specific genes of interest will be analyzed using RT-PCR
for subjects with pustular palmo-plantar psoriasis and non-pustular palmo-plantar psoriasis.
Moreover, four skin biopsies will be collected from 10 healthy volunteers for RT-PCR (IL-23
(p40 & p19), IL-17A and HARP). One biopsy will be collected from the trunk and another one
from a palm or a sole. A third and a fourth biopsy will be collected on additional areas
(scalp, elbow or lower limb). Gene expression in plaques from areas more resistant to
treatment (scalp, palms, elbows, lower legs) will be compared to gene expression in plaques
from the trunk or other areas of the upper and lower limbs.
A total of 30 subjects out of 80 will also have one or two additional skin biopsies. The 10
subjects with pustular palmo-plantar psoriasis and 10 subjects with non-pustular
palmo-plantar psoriasis will have one additional biopsy of the involved skin of the palm and
one of a plaque on the trunk or limbs for cell isolation and cell analysis in order to
explore the mechanisms involved in the increased expression of IL-17A without concurrent
increase in IL-23. Ten subjects with psoriasis vulgaris on the trunk or upper limbs but
without pustular or non-pustular palmo-plantar psoriasis will also have an additional biopsy
performed on lesional skin. Following inflammatory cells extraction, flow cytometry
combining cell surface markers and intra-cytoplasmic staining will be used to study IL-17A
and IL-23 in T cells, granulocytes/mastocytes/macrophages and Ag-presenting cells. If enough
cells are harvested, three antibody panels will be analyzed in the following order using
flow cytometry: a T cell panel, a granulocytes / mastocytes / macrophages panel and an
antigen presenting cell (APC) panel. All panels with also be evaluated with an anti-CD45
(cluster of differentiation) antibody and a viability test (Aqua live/dead). Results from
flow cytometry will be compared for biopsies from palms of subjects with pustular and
non-pustular palmo-plantar psoriasis, trunk or proximal limbs of subjects with pustular and
non-pustular palmo-plantar psoriasis and trunk or proximal limbs of subjects with psoriasis
vulgaris.
All skin biopsies will be performed at Day 0 visit and an optional study visit (Day 10) will
be performed if suture removal from skin biopsies is necessary.
In addition, circulating plasma levels of IL-17A will be measured for all subjects and
healthy volunteers in order to compare IL-17A levels in the 5 groups of subjects with
psoriasis and healthy subjects. Moreover, correlation between IL-17A levels and PASI will be
explored.
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Observational Model: Cohort, Time Perspective: Cross-Sectional
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