Patterns of circulating autoantibodies against desmoglein-1 and desmoglein-3 in the progression of oral lichen planus: A scoping review

IF 2.3 4区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Archives of oral biology Pub Date : 2026-01-01 Epub Date: 2025-10-17 DOI:10.1016/j.archoralbio.2025.106431
Andari Sarasati , Kadek Gede Putra Wibawa , Meircurius Dwi Condro Surboyo , Rene Luis Panico , Arvind Babu Rajendra Santosh , Adhistya Viany , Dewi Agustina , Diah Savitri Ernawati
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引用次数: 0

Abstract

Objective

The potential role of autoantibodies targeting desmosomal proteins, particularly desmoglein 1 (Dsg-1) and desmoglein 3 (Dsg-3), in modulating disease severity and epithelial integrity in oral lichen planus (OLP) remains a subject of growing interest. Distinct patterns of anti-Dsg-1 and anti-Dsg-3 autoantibodies across OLP subtypes may correlate with disease progression. This scoping review investigates the expression patterns of circulating anti-Dsg-1 and anti-Dsg-3 autoantibodies in reticular, erosive, and ulcerative forms of OLP to elucidate their potential roles in epithelial disruption and disease advancement.

Design

Following PRISMA guidelines, a systematic search of four electronic databases was conducted. Eligible studies included case reports, case series, case-control and cross-sectional studies that reported serum levels of anti-Dsg-1 and anti-Dsg-3 autoantibodies in OLP patients.

Results

Reticular-type OLP showed variable anti-Dsg-1 and anti-Dsg-3 autoantibody levels, with some patients testing positive while others were negative, indicating an inconsistent involvement of desmosomal autoimmunity in this milder form of the disease.
In erosive-type OLP, the presence of both autoantibodies indicated deeper epithelial damage and an active autoimmune response. Interestingly, ulcerative-type OLP consistently tested negative for both antibodies despite extensive epithelial breakdown, implying a potential shift from desmosomal autoimmunity to chronic inflammation–driven tissue destruction that could compromise human health.

Conclusion

These findings suggest a potential continuum in which reticular OLP may progress to erosive OLP, with Dsg-3 autoantibodies as a possible early marker of worsening pathology. Ulcerative OLP appears to represent a late-stage, inflammation-driven phenotype with minimal autoantibody involvement. Given the limited and heterogeneous data, these observations are preliminary and should be interpreted cautiously.
口腔扁平苔藓发展过程中抗粘连蛋白-1和粘连蛋白-3循环自身抗体的模式:范围综述。
目的:针对桥粒蛋白的自身抗体,特别是桥粒蛋白1 (Dsg-1)和桥粒蛋白3 (Dsg-3),在调节口腔扁平苔藓(OLP)疾病严重程度和上皮完整性方面的潜在作用仍然是一个越来越受关注的主题。不同OLP亚型的抗dsg -1和抗dsg -3自身抗体的不同模式可能与疾病进展相关。本综述研究了网状、糜烂和溃疡性OLP中循环抗dsg -1和抗dsg -3自身抗体的表达模式,以阐明它们在上皮破坏和疾病进展中的潜在作用。设计:按照PRISMA的指导方针,系统地检索了四个电子数据库。符合条件的研究包括报告OLP患者血清抗dsg -1和抗dsg -3自身抗体水平的病例报告、病例系列、病例对照和横断面研究。结果:网状型OLP显示抗dsg -1和抗dsg -3自身抗体水平变化,一些患者检测呈阳性,而另一些患者检测呈阴性,表明在这种较轻形式的疾病中,桥粒体自身免疫的参与不一致。在糜烂型OLP中,两种自身抗体的存在表明更深的上皮损伤和积极的自身免疫反应。有趣的是,尽管有广泛的上皮破坏,溃疡型OLP的两种抗体检测结果始终呈阴性,这意味着从桥粒体自身免疫到慢性炎症驱动的组织破坏的潜在转变,可能危及人类健康。结论:这些发现表明网状OLP可能发展为糜烂性OLP, Dsg-3自身抗体可能是病理恶化的早期标志。溃疡性OLP似乎代表了一种晚期,炎症驱动的表型,自身抗体参与最小。考虑到有限和异质性的数据,这些观察结果是初步的,应该谨慎解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Archives of oral biology
Archives of oral biology 医学-牙科与口腔外科
CiteScore
5.10
自引率
3.30%
发文量
177
审稿时长
26 days
期刊介绍: Archives of Oral Biology is an international journal which aims to publish papers of the highest scientific quality in the oral and craniofacial sciences. The journal is particularly interested in research which advances knowledge in the mechanisms of craniofacial development and disease, including: Cell and molecular biology Molecular genetics Immunology Pathogenesis Cellular microbiology Embryology Syndromology Forensic dentistry
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