Immune mechanisms in oral lichen planus.

T cell antigen presenting cell keratinocyte mast cell oral disease oral lichen planus

Journal

Oral diseases
ISSN: 1601-0825
Titre abrégé: Oral Dis
Pays: Denmark
ID NLM: 9508565

Informations de publication

Date de publication:
May 2023
Historique:
revised: 12 01 2022
received: 17 10 2021
accepted: 17 01 2022
medline: 21 4 2023
pubmed: 30 1 2022
entrez: 29 1 2022
Statut: ppublish

Résumé

Oral lichen planus (OLP) is a T cell-mediated inflammatory disease of the oral mucosa that has been extensively researched over many years but as yet the mechanisms of pathogenesis are still not fully understood. Whilst the specific aetiological factors driving OLP remain ambiguous, evidence points to the development of a chronic, dysregulated immune response to OLP-mediating antigens presented by innate immune cells and oral keratinocytes leading to increased cytokine, chemokine and adhesion molecule expression. These molecules recruit T cells and mast cells to the diseased site and orchestrate a complex interplay between cells that culminates in keratinocyte cell death, mucosal basement membrane destruction and long-term chronicity of the disease. The main lymphocytes involved are thought to be CD8+ cytotoxic and CD4+ Th1 polarised T cells although recent evidence indicates the involvement of other Th subsets such as Th9, Th17 and Tregs, suggesting that a more complex immune cell relationship exists during the disease process. This review provides an overview of the immune mechanisms at play in OLP pathogenesis with particular emphasis on the role of the different Th subsets and how these recent discoveries may guide research towards identifying potential therapeutic targets.

Identifiants

pubmed: 35092132
doi: 10.1111/odi.14142
doi:

Substances chimiques

Cytokines 0

Types de publication

Journal Article Review

Langues

eng

Pagination

1400-1415

Informations de copyright

© 2022 Wiley Periodicals LLC.

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Auteurs

Asma El-Howati (A)

School of Clinical Dentistry, University of Sheffield, Sheffield, United Kingdom.
Faculty of Dentistry, Department of Oral Medicine, University of Benghazi, Benghazi, Libya.

Martin H Thornhill (MH)

School of Clinical Dentistry, University of Sheffield, Sheffield, United Kingdom.

Helen E Colley (HE)

School of Clinical Dentistry, University of Sheffield, Sheffield, United Kingdom.

Craig Murdoch (C)

School of Clinical Dentistry, University of Sheffield, Sheffield, United Kingdom.

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