Comparison of tyrosinase antibody, tyrosinase-related protein-1 and-2 antibodies, melanin-concentrating hormone receptor antibody levels with autologous serum skin test and autologous plasma skin test results in patients with vitiligo

dc.contributor.authorUnal, Abdullah
dc.contributor.authorOzkol, Hatice Uce
dc.contributor.authorBayram, Yasemin
dc.contributor.authorAkdeniz, Necmettin
dc.date.accessioned2025-05-10T19:31:36Z
dc.date.issued2021
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractIntroduction: Although the exact etiopathogenesis of vitiligo is unknown, the autoimmunity hypothesis is much in evidence. The autologous serum skin test (ASST) and autologous plasma skin test (APST) are in vivo methods used in the diagnosis of some autoimmune diseases, which are easy and inexpensive to perform. Aim: In this study, we investigated whether or not ASST and APST could determine autoimmunity in patients with vitiligo. Material and methods: In this study, 30 vitiligo patients presenting to the dermatology outpatient clinic and 30 healthy volunteers without any known autoimmune diseases were included. Antibodies such as tyrosinase, tyrosinase-related protein-1 (TYRP1), tyrosinase-related protein-2 (TYRP2) and melanin-concentrating hormone receptor 1 (MCHR1) antibodies determined to be associated with vitiligo were examined. In addition, the association of these antibodies with the positivity of ASST and APST, which were suggested to be associated with autoimmunity, were examined. Results: In our study, tyrosinase antibody was found to be significantly higher in vitiligo patients. ASST was positive in 12 (40%) patients with vitiligo and 8 (26.6%) control subjects. APST was positive in 8 (26.6%) of the patients with vitiligo and in 2 (6.6%) of the controls, and there was a significant difference between the groups in terms of APST positivity (p = 0.032). In addition, in our study, a significant correlation was found between TYRP1 antibody positivity and APST positivity in the patient group (p = 0.005). Conclusions: These findings suggest that we may use APST to investigate the autoimmune etiopathogenesis of vitiligo.
dc.description.sponsorshipVan YYU - BAP
dc.description.sponsorshipVan YYU - BAP provided financial support to this clinical trial.
dc.identifier.doi10.5114/ada.2020.93272
dc.identifier.endpage479
dc.identifier.issn1642-395X
dc.identifier.issn2299-0046
dc.identifier.issue3
dc.identifier.pmid34377130
dc.identifier.scopus2-s2.0-85112726310
dc.identifier.scopusqualityQ2
dc.identifier.startpage473
dc.identifier.urihttps://doi.org/10.5114/ada.2020.93272
dc.identifier.urihttps://hdl.handle.net/20.500.14730/7976
dc.identifier.volume38
dc.identifier.wosWOS:000678928900019
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTermedia Publishing House Ltd
dc.relation.ispartofPostepy Dermatologii I Alergologii
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectvitiligo
dc.subjectautoimmunity
dc.subjectantibodies
dc.subjectautologous serum skin test
dc.titleComparison of tyrosinase antibody, tyrosinase-related protein-1 and-2 antibodies, melanin-concentrating hormone receptor antibody levels with autologous serum skin test and autologous plasma skin test results in patients with vitiligo
dc.typeArticle

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