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

C

Centre Hospitalier Universitaire de Nice

Status

Enrolling

Conditions

Psoriasis

Treatments

Other: Biopsy and venous blood

Study type

Interventional

Funder types

Other

Identifiers

NCT05399433
21-PP-25

Details and patient eligibility

About

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,

Enrollment

100 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Production of IL-23 of blood and skin dendriti cells (CD)
Other group
Description:
Simultaneously evaluate the migratory capacity and production of IL-23 of blood and skin cDC on peripheral venous blood and skin biopsies of psoriatic patients with and without type 2 diabetes and control patients (with or without type II diabetes) depending on their metabolic status.
Treatment:
Other: Biopsy and venous blood

Trial contacts and locations

1

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Central trial contact

PASSERON Thierry, PhD

Data sourced from clinicaltrials.gov

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