Replicative Stress in Hair Follicle Stem Cells and Pathogeny of Hidradenitis Suppurativa

NCT ID: NCT05531747

Last Updated: 2025-02-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-06-13

Study Completion Date

2029-12-13

Brief Summary

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Hidradenitis Suppurativa is a recurrent chronic inflammatory follicular occlusive disease affecting hair follicles. HS is notoriously difficult and challenging to treat with a high morbidity impact and could be classified as an unmet medical need with no efficient therapeutic options.

Objective:

Investigators previously showed that Outer Root Sheath Cells (ORS) isolated from hair follicle of HS patients (HS-ORS) have a pro-inflammatory phenotype and secrete spontaneously IP-10 and RANTES. To identify the mechanisms involved in the pro-inflammatory phenotype of HS-ORS, investigators performed a transcriptomic analysis in healthy and HS patients. This revealed: (i) an IFN signature, (i) a dysregulation of genes involved in cell proliferation and differentiation, and (iii) an upregulation of DNA damage response and cell cycle G2/M checkpoint pathways in HS-ORS. These findings support the notion that, in HS patients, a perturbation of HF-SC homeostasis leading to an increased proliferation induces a replicative stress and an accumulation of cytoplasmic ssDNA, stimulating IFN synthesis through IFI16-STING pathway. Interestingly, replicative stress in ORS were present in some but not all patients with Hidradenitis Suppurativa. The goal of study is to determine replicative stress in ORS in a large cohort of HS patients.

Method Patients will be enrolled in the Mondor Dermatology department, during routine care. A dermatologist will check all inclusion and exclusion criteria with the technical support of a research technician of the Henri Mondor Clinical Investigation Center. Medical history, clinical data, comorbidities and concomitant therapies will be prospectively recorded in a dedicated case report form. Skin biopsies will be performed in perilesional zone rich in hair follicles. mRNA will be extracted from freshly isolated hair follicle cells and some slides will be prepared and stored at -80°C to perform immunohistochemistry analysis on freshly isolated hair follicle cells. PBMC and serum will be collected.

All these biological samples will allow us to quantify the replicative stress in HS-ORS of each patient, and to quantify several cytokine of interest : IFN de type 1, IL-17, IL-6, TNF-α, IL-10

This study will allow investigators to evaluate the rate of patients with replicative stress in hair follicle stem cells in Hidradenitis Suppurativa. The investigator will also determine whether HF-SC replication stress correlates with clinical characteristics and/or with clinical course and/or comorbidities.

Detailed Description

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Conditions

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Hidradenitis Suppurativa

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Biological assays will be performed by technician blinded from patients clinical status

Study Groups

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Physiopathologic exploration

A non randomised study with one arm, addind experimental acts to standard of care (skin biopsy and biological sample ) in order to explore Hidradenitis Suppurativa physiopathology

Group Type EXPERIMENTAL

Skin biopsy

Intervention Type OTHER

A maximum of 2 superficial skin biopsies (epidermis/dermis), allowing 10 hair follicles to be obtained, at the edge of the affected area, in healthy territory (excluding the face and folds but not excluding the pubic region), at initiation visit.

Blood sample

Intervention Type OTHER

42mL of blood (6 tubes of 7mL) sampled at initiation visit

Interventions

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Skin biopsy

A maximum of 2 superficial skin biopsies (epidermis/dermis), allowing 10 hair follicles to be obtained, at the edge of the affected area, in healthy territory (excluding the face and folds but not excluding the pubic region), at initiation visit.

Intervention Type OTHER

Blood sample

42mL of blood (6 tubes of 7mL) sampled at initiation visit

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients referred to the consultation of dermatology of Henri Mondor Hospital
* Diagnosis of Hidradenitis Suppurativa
* Age\> 18 y.o.
* Affiliation to a social security system

Exclusion Criteria

* Patient under tutorship or curatorship
* Breastfeeding or pregnant women
* Refusal to sign the consent letter
* Patients benefiting from State Medical Aid
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Assistance Publique Hôpitaux de Paris - CHU Henri Mondor

Créteil, Val-de-marne, France

Site Status RECRUITING

Countries

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France

Central Contacts

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Claire HOTZ, MD

Role: CONTACT

33-1-49-81-37-96

Philippe Le Corvoisier, MD PhD

Role: CONTACT

33-1-49-81-37-96

Facility Contacts

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Claire HOTZ, MD-PhD

Role: primary

33-1-49-81-45-11

Philippe Le Corvoisier, MD-pHD

Role: backup

33-1-49-81-37-96

Other Identifiers

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APHP211351

Identifier Type: -

Identifier Source: org_study_id

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