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- Title
Patients suffering from dystrophic epidermolysis bullosa are prone to developing autoantibodies against skin proteins: A longitudinal confirmational study.
- Authors
Bremer, J.; Pas, H. H.; Diercks, G. F. H.; Meijer, H. J.; van der Molen, S. M.; Nijenhuis, A. M.; van Nijen‐Vos, L. L.; Morandé, P.; Yubero, M. J.; Palisson, F.; Fuentes, I.; Pasmooij, A. M. G.
- Abstract
Epidermolysis bullosa (EB) is a heritable skin blistering disease caused by variants in genes coding for proteins that secure cell–cell adhesion and attachment of the epidermis to the dermis. Interestingly, several proteins involved in inherited EB are also associated with autoimmune blistering diseases (AIBD). In this study, we present a long‐term follow‐up of 15 patients suffering from recessive dystrophic or junctional EB. From these patients, 62 sera were analysed for the presence of autoantibodies associated with AIBD. We show that patients suffering from recessive dystrophic EB (RDEB) are more susceptible to developing autoantibodies against skin proteins than patients suffering from junctional EB (70% vs. 20%, respectively). Interestingly, no correlation with age was observed. Most patients showed reactivity to Type XVII collagen/linear IgA bullous dermatosis autoantigen (n = 5; 33%), followed by BP230 (n = 4; 27%), Type VII collagen (n = 4; 27%) and laminin‐332 (n = 1; 7%). The pathogenicity of these autoantibodies remains a subject for future experiments.
- Subjects
SKIN proteins; EPIDERMOLYSIS bullosa; AUTOANTIBODIES; LONGITUDINAL method; GENETIC code
- Publication
Experimental Dermatology, 2024, Vol 33, Issue 2, p1
- ISSN
0906-6705
- Publication type
Case Study
- DOI
10.1111/exd.15035