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Recruiting Not applicable

Role of Glucose Metabolism in Migration of Cutaneous Dendritic Cells in Psoriasis

NCT05399433 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-06-30
Last updated
2026-10-01

Condition(s) studied

Psoriasis

Investigational drug(s) / intervention(s)

Biopsy and venous blood

Biopsy and venous blood: A skin biopsy will be performed under local anesthesia in diabetic and non-diabetic psoriatic patients (25 per group) in the injured area (joint extension) and in the non-injured area more than 2 cm from any lesion in the same area. In patients in the diabetic or non-diabetic control group (25 per group) only one biopsy will be performed. Peripheral venous blood will be collected in heparin tubes for metabolic parameter analysis and blood CD analysis

Study summary

Dendritic cells (DC) paly a key role in the induction and chronicity of psoriasis by capturing the antigenes and activating the T cell repsonse. This activation requires their migration from the cutaneous sensitisation site to the lymph nodes. This migration requires an important intracellular metabolic activity, with a strong involvmenet of glucdic metabolism. This activity is linked with the systemic activity. This study aims to compare the migration and the phenotypic and metabolic caracteristics of blood and skin DCs in patients with or without psoriasis and with or without type 2 diabetes,

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Patients of both sexes * hospitalized in the Dermatology department of the CHU of Nice for moderate to severe psoriasis (defined by a PASI \> or = 10) * covered by a social security scheme after obtaining a free * Clinical diagnosis of plaque psoriasis by a dermatologist with or without type 2 diabetes (defined by glycated hemoglobin \>7%) * For the control group: without psoriasis or other inflammatory dermatosis aged in the presence or not of type 2 diabetes (glycated hemoglobin \>7%). * free and informed consent Exclusion Criteria: * Minor or incapable or unwilling to consent freely or in an informed manner Pregnant or nursing woman. * Patient in a period of exclusion from other biomedical research * Patient with generalized chronic inflammatory disease or other inflammatory dermatosis * Patients on general corticosteroid, immunomodulator or immunosuppressant therapy in the month prior to local inclusion or treatment with corticosteroid therapy in the 15 days prior to inclusion, on anti- treatmentIL-23 or anti IL12/23 for less than 3 months or under anti-IL-17 or anti-TNF treatment for less than 1 month. * Contraindication to cutaneous biospsis (known hemostasis disorder, taking anticoagulants, allergy to xylocaine, history of cheloid scars, congenital immune deficiency)

Primary outcome measure(s)

  • Percentage of dentridic cells producers of IL-23 — at baseline
    Alterations in the percentage of dentridic cells that have migrated with the metabolic status of patients

Trial sites (1)

FacilityCityRegionStatus
CHU de Nice Nice Alpes-maritimes Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05399433 on ClinicalTrials.gov ↗ ← All trials in France