학술논문

New insight of itch mediators and proinflammatory cytokines in epidermolysis bullosa
Document Type
article
Source
Journal of Cutaneous Immunology and Allergy, Vol 5, Iss 3, Pp 78-87 (2022)
Subject
cytokines
dystrophic epidermolysis bullosa pruriginosa
IL‐1β
IL‐31
IL‐4
IL‐6
Dermatology
RL1-803
Immunologic diseases. Allergy
RC581-607
Language
English
ISSN
2574-4593
Abstract
Abstract Objectives Epidermolysis bullosa (EB) is a hereditary disorder characterized by mechanical stress‐induced blistering. The presence of extracutaneous complications such as cardiomyopathy and renal disease observed in severe EB subtypes and the fact that pruritus is a common symptom across all EB subtypes indicate that EB is not only a skin fragility disease but also a systemic inflammatory disorder. Our study aims to elucidate the basis of the systemic inflammation seen in EB patients. Methods We analyzed serum samples of 20 EB patients by Luminex bead‐based cytokine assays and enzyme‐linked immunosorbent assays. Results The serum levels of sIL‐2R, IL‐6, HGF, M‐CSF, SCGF‐β, IL‐8, IL‐16, IFN‐γ, MIF, MIP‐1α, and thymic stromal lymphopoietin (TSLP) (p