Clinical Trials Directory

Trials / Completed

CompletedNCT02883894

Interest of Dosage of Anti-PB230, Anti-PB180 and Cytokines for Monitoring of Patients Suffering From Bullous Pemphigoid

Status
Completed
Phase
Study type
Observational
Enrollment
120 (actual)
Sponsor
CHU de Reims · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Bullous pemphigoid is the most common subepidermal autoimmune blistering disease of the skin in European countries, including France. Immunologically, BP is characterized by the production of autoantibodies directed against two major components of the hemidesmosome, BP180 and BP230. The anti-BP180 autoantibody is detected in 79-93% of cases of bullous pemphigoid and its serum level at diagnosis have been correlated with disease activity. The anti-BP230 autoantibody is detected in 57%-63% of bullous pemphigoid cases and its score at diagnosis did not correlate with disease activity. Up to now, no clinical or immunologic factors have been identified to predict outcome of patients with good or poor prognosis bullous pemphigoid as defined by long complete remission off therapy and recurrent disease requiring maintenance therapy for years. The usefulness of BP180 or BP230 ELISA scores for monitoring BP patients during treatment also remains unclear.

Detailed description

Aim of the study were : To study association between the serum level of cytokines (IL-17 and IL-23) and of the protease MMP-9 and the relapse of bullous pemphigoid.

Conditions

Interventions

TypeNameDescription
OTHERBlood sample for dosages of cytokines (IL-17 and IL-23) and of the protease MMP-9

Timeline

Start date
2009-11-01
Primary completion
2012-04-01
Completion
2014-04-01
First posted
2016-08-30
Last updated
2016-08-30

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02883894. Inclusion in this directory is not an endorsement.