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Recruiting Not applicable

Cellular and Molecular Biomarkers in Patients With Lichen Planus

NCT06451744 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-11-01
Last updated
2025-07-01

Condition(s) studied

Lichen Planus

Investigational drug(s) / intervention(s)

Blood samples collectionSkin or mucous membrane brushingSkin or mucous membrane biopsy

Blood samples collection: 50 mL blood sample

Skin or mucous membrane brushing: brushing on skin or mucous membrane lesions

Skin or mucous membrane biopsy: 6 mm biopsy

Study summary

Lichen planus (LP) is a chronic inflammatory disease of unknown aetiology, affecting the skin and mucous membranes, characterised by a CD8+ cytotoxic T-cell infiltrate, associated with epithelial cell death and disruption of the basement membrane zone. In previous work, T cell antigen receptor (TCR) repertoire studies were performed. In all patients tested, whether with erosive or non-erosive LP, unique nucleotide sequences, called clonotypes, have been identified. They appear during the process of TCR gene rearrangement. These clonotypes are specific for human papillomavirus (HPV) in blood and lesions, suggesting antigenic stimulation of these clonotypes by a viral epitope of HPV, which crosses with an epitope on keratinocytes. The diagnosis of LP is made on the basis of clinical and histological criteria, but in some patients and in some anatomical locations, the diagnosis is difficult to make and LP may be confused with other skin conditions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Subject coming at the time of diagnosis of the disease before any systemic treatment, or at the time of a progressive episode of the disease, without systemic treatment or after cessation of immunomodulatory or immunosuppressive treatment * Ability to give their consent in writing * Must understand spoken and written French * Affiliated to the French social security or assimilated regimes Exclusion Criteria: * Dermatosis exclusively localised in the skin folds or on the face (risk of scarring from biopsies)

Primary outcome measure(s)

  • Identification of TCR repertoire by flow cytometry — 3 years
    Determination by flow cytometry and PCR testing for TCR repertoire bias

Trial sites (6)

FacilityCityRegionStatus
CHU de Besançon Besançon France Recruiting
CHU Paris Seine-Saint-Denis- Hôpital Avicenne Bobigny France Recruiting
Centre Medical de l'Institut Pasteur Paris France Recruiting
Hôpital Saint-Louis Paris France Recruiting
Hôpital Robert Debré, CHU de Reims Reims France Recruiting
CHU de Rouen Rouen France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06451744 on ClinicalTrials.gov ↗ ← All trials in France