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Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment
Author(s) -
Castela E.,
Tulic M.K.,
Rozières A.,
Bourrat E.,
Nicolas J.F.,
Kanitakis J.,
Vabres P.,
Bessis D.,
Mazereeuw J.,
MoricePicard F.,
Baty D.,
Berard F.,
Lacour J.P.,
Passeron T.,
Chiaverini C.
Publication year - 2019
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.16897
Subject(s) - epidermolysis bullosa simplex , medicine , epidermolysis bullosa , pathogenesis , apremilast , inflammation , pathology , cytokine , psoriasis , immunology , dermatology , psoriatic arthritis
Summary Background Epidermolysis bullosa simplex generalized severe ( EBS ‐gen sev) is a genetic disorder caused by mutation in the KRT 5 or KRT 14 genes. Although it is usually considered a mechanical disease, recent data argue for additional inflammatory mechanisms. Objectives To assess the inflammation in the skin of patients with EBS ‐gen sev. Methods A first immunohistochemical retrospective study was performed on frozen skin samples from 17 patients with EBS ‐gen sev. A second multicentre prospective study was conducted on 10 patients with severe EBS ‐gen sev. Blister fluid and epidermis were processed for immunochemical analysis and quantitative real‐time polymerase chain reaction. Cytokine expression was analysed in blister fluid and compared with that in controls. Results Histological analysis showed a constant dermal perivascular CD 4 + lymphocyte infiltrate in skin biopsies of both blister ( n = 17) and rubbed skin ( n = 5), an epidermal infiltration of neutrophils and eosinophils in 70% of cases, and increased immunostaining for CXCL 9 and CXCL 10 in blistering skin. High levels of T helper 17 cytokines were detected in lesional skin. Three adult patients with EBS ‐gen sev were treated with apremilast, with a dramatic improvement of skin blistering and good tolerance. Conclusions Our study demonstrates the importance of inflammation in patients with EBS ‐gen sev and underlines the key role for T helper 17 cells in its pathogenesis. In addition, this study provides promising new therapeutic approaches for this disabling disorder.