Deciphering IL-17-dependant Inflammatory Response in Bullous Pemphigoid

Phase

N/A

Condition

Epidermolysis Bullosa

Pemphigus Vulgaris (Pv)

Treatment

Cutaneous biopsy

Blood sampling

Liquid bubble sampling

Clinical Study ID

NCT06479018

PO21096

Ages > 18
All Genders

Study Summary

Bullous pemphigoid (BP) is the most frequent autoimmune skin disease and mainly affects elderly individuals. BP classically manifests with tense blisters over urticarial plaques on the trunk and extremities accompanied by intense itches. However, BP is characterized by a large spectrum of clinical presentations allowing to distinguish between typical (with blisters) and atypical forms (non bullous, mucosal damage).

High potency topical steroids and systemic steroids are the current first line intention treatments. While very efficient, these therapies are non-targeted and cause numerous side-effects, especially in these elderly patients that are the most affected. Furthermore, around 30% of BP patients will relapse during the first year of treatment when corticotherapy is decreased or stopped.

The investigators and others have highlighted the presence of Il-17 family belonging-inflammatory cytokines in BP patients. Their functions in the amplification of the inflammatory response and in the mechanisms of relapse have to be precisely determined in order to develop innovative therapeutic approaches and to move forwards precision medicine.

Eligibility Criteria

Inclusion

Inclusion Criteria:

patients with Bullous Pemphigoid (BP) using the following criteria: clinicalfeatures typical of BP with presence of at least three out of four well-establishedcriteria by Vaillant et al.47; subepidermal blister on skin biopsy; and deposits ofIgG and/or C3 in a linear pattern along the epidermal basement membrane zone bydirect IF.
patient agreed to participate to the study
patient affiliated to the French Healthcare System

Exclusion

Exclusion Criteria:

patient that does not have the ability to give its written informed consent beforeinclusion in the study
patient with a pemphigoid gestationis
patient with a relapse of Bullous Pemphigoid
patient with Bullous Pemphigoid that already received local superpotentcorticotherapy during the last 14 days before inclusion or systemic corticoidtreatment during the last 28 days before inclusion
anemic patient (hemoglobin < 10 g/dL)

Study Design

Cutaneous biopsy

February 10, 2022

January 10, 2026

Study Description

This is a pathophysiological study with prospective and monocentric inclusion.

90 patients with bullous phemphigoid will be recruited from the department of dermatology at the Reims University Hospital.

The main objectives of this study are to identify the cellular and molecular actors of the IL-17B/IL-17RB axis at diagnosis in patients with bullous pemphigoid and to determine their functions in the pathophysiological mechanisms associated with BP at systemic and in situ levels.

The secondary aims of this research are:

To confirm IL-17B concentrations in sera at diagnosis as predictive biomarker of BP outcome under local corticotherapy
To study the expression kinetics of IL-17B and its receptor IL-17RB in BP patients under treatment
To study the implication of IL-17B/IL-17RB axis in BP relapse
To establish inflammatory cell composition profile in skin and blood issued from clinical variants of BP as well as from BP patients during the first year of treatment.

Connect with a study center

Chu Reims
Reims, 51092
France
Active - Recruiting

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