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.
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. Several triggers have been proposed for LP, including viral antigens. In previous work, T cell antigen receptor (TCR) repertoire studies were performed, i.e. investigating the diversity of TCRs expressed on the surface of an individual's lymphocyte population. 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.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
70
50 mL blood sample
brushing on skin or mucous membrane lesions
6 mm biopsy
CHU de Besançon
Besançon, France
RECRUITINGCHU Paris Seine-Saint-Denis- Hôpital Avicenne
Bobigny, France
RECRUITINGCentre Medical de l'Institut Pasteur
Paris, France
RECRUITINGHôpital Saint-Louis
Paris, France
RECRUITINGHôpital Robert Debré, CHU de Reims
Reims, France
RECRUITINGCHU de Rouen
Rouen, France
RECRUITINGIdentification of TCR repertoire by flow cytometry
Determination by flow cytometry and PCR testing for TCR repertoire bias
Time frame: 3 years
Identification of characteristic biomarkers of lichen
Identify complementary biomarkers characterising lichen by quantitative PCR
Time frame: 3 years
Identification of T CD8 clonotypes
Measurement of the antigenic specificity of identified T CD8 clonotypes by flow cytometry
Time frame: 3 years
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