Clinico-biological Collection of Autoimmune, Dysimmune or Auto-inflammatory Dermatological Diseases

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age6-99
SponsorUniversity Hospital, Toulouse

About this trial

The aim of this project is to start a biological and clinical collection of patients presenting autoimmune, dysimmune or auto-inflammatory dermatological diseases. This collection will provide appropriate biological samples to identify new biomarkers and to be accessible to the medical, scientific and industrial communities for the identification of new therapeutic strategies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with autoimmune bullous dermatoses (pemphigus, pemphigoid and others),

Patients with systemic autoimmune diseases associated with skin damage (lupus, scleroderma, dermatomyositis for example),

Patients with cutaneous lupus

Patients with dysimmune skin diseases (psoriasis, eczema)

Disqualifiers

Patients under protective supervision (guardianship, curators)

Patients under 6 years old

Pregnant or breastfeeding woman

Trial population

Patients with autoimmune, dysimmune or auto-inflammatory dermatological disease

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Blood sampling

    Biological/Vaccine

    Blood will be taken in larger quantity

  • Remainders of samples taken as part of the treatment

    Biological/Vaccine

    blood, CSF, saliva, stools, urine, other biological fluids and tissue biopsies, hair follicles

Treatment groups

800 Participants
are divided into 1 treatment group
Group A: Patients suffering from autoimmune, dysimmune or auto-inflammatory dermatological disease2 interventions

Trial outcomes

Primary outcomes

1

Building a collection of biological samples and clinical-biological data from patients with autoimmune, dysimmune or auto-inflammatory dermatological disease

Blood sampling

Time frame
Day 0 and through study completion, an average of 1 year

Secondary outcomes

1

Identification of new autoantibodies

Western blot or immunoprecipitation method

Time frame
Day 0 and through study completion, an average of 1 year
2

Identification of biomarkers regarding the severity (such as cytokines, survival factors) in order to help the therapeutic decisions

Proteomic analysis of sera and plasma samples at diagnosis and during follow up

Time frame
Day 0 and through study completion, an average of 1 year
3

Exploration of the pathophysiological mechanisms of rare autoimmune dermatological pathologies

Knock-out or knock-in animal models for one specific protein will be used to determine in vivo if the pathophysiological mechanisms of Dermatological Diseases can be induced by the abnormal expression of this protein. Analysis of the phenotypic profiling of blood immune cells by multicolor fluorescence-activated cell sorter (FACS) analysis and of the transcriptomic profiling of blood immune cells by RNA sequencing

Time frame
Day 0 and through study completion, an average of 1 year
4

Comparison of blood cells populations determinants with flow cytometry, before and after cell therapy and in patients responder or not responder to cell therapy

Exploring blood cell populations before and after cell therapy with flow cytometry

Time frame
Day 0 and through study completion, an average of 1 year

Other outcomes

Sponsors and contacts

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