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Published in: Archives of Dermatological Research 4/2015

01-05-2015 | Original Paper

Regulation of immune cells in oral lichen planus

Authors: F. A. Firth, L. T. Friedlander, V. P. B. Parachuru, T. B. Kardos, G J. Seymour, A. M. Rich

Published in: Archives of Dermatological Research | Issue 4/2015

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Abstract

Oral lichen planus (OLP) is an immunological disease and while it is understood that the T cell subsets, FoxP3+ Tregs and IL17+ Th17 cells are involved in immune regulation, little is known about their presence in OLP. The aims of this study were to compare the number of cells expressing FoxP3 or IL-17 in OLP with non-specifically inflamed oral mucosa and to determine which cell types expressed FoxP3 and/or IL-17 and their distribution. Immunohistochemistry was used to investigate the presence of FoxP3+ or IL-17+ cells in 12 control cases and 17 cases of OLP. These results were analysed quantitatively and qualitatively. Double-labelling immunofluorescence (IF) was used to determine the type of cell expressing FoxP3/IL-17 and these results were analysed qualitatively. OLP displayed significantly more FoxP3+ cells (mean 79.3 vs. 20.6 cells/defined area, p < 0.0001) and fewer IL-17+ cells (mean 1.05 vs. 3.30 cells/defined area, p = 0.0003) than non-specific inflammatory cases. The majority of FoxP3+ cells were in the sub-epithelial infiltrate, while IL-17+ cells were deeper in the stromal tissues. IF showed that FoxP3+ cells co-localised with T cells, while the IL-17+ cells did not. These results show that the balance between Tregs and IL-17+ cells is altered in OLP, thus supporting the proposition that disturbance in local immune regulation is important in the pathogenesis of OLP. The observation that the IL-17+ cells were mast cells has not previously been reported in OLP and again raises questions about the role of mast cells in this condition.
Literature
1.
go back to reference Beriou G, Costantino CM, Ashley CW, Yang L, Kuchroo VK, Baecher-Allan C et al (2009) IL-17-producing human peripheral regulatory T cells retain suppressive function. Blood 113:4240–4249CrossRefPubMedCentralPubMed Beriou G, Costantino CM, Ashley CW, Yang L, Kuchroo VK, Baecher-Allan C et al (2009) IL-17-producing human peripheral regulatory T cells retain suppressive function. Blood 113:4240–4249CrossRefPubMedCentralPubMed
2.
go back to reference Chen X, O’Shea JJ (2008) Regulation of IL-17 production in human lymphocytes. Cytokine 41:71–78CrossRefPubMed Chen X, O’Shea JJ (2008) Regulation of IL-17 production in human lymphocytes. Cytokine 41:71–78CrossRefPubMed
3.
4.
go back to reference Davari P, Hsiao HH, Fazel N (2014) Mucosal oral lichen planus: an evidence—based treatment update. Am J Clin Dermatol 15:181–195CrossRefPubMed Davari P, Hsiao HH, Fazel N (2014) Mucosal oral lichen planus: an evidence—based treatment update. Am J Clin Dermatol 15:181–195CrossRefPubMed
5.
go back to reference Di Stasio D, Guida A, Salerno C, Contaldo M, Esposito V, Laino et al (2014) Oral lichen planus: a narrative review. Front Biosci 6:370–376CrossRef Di Stasio D, Guida A, Salerno C, Contaldo M, Esposito V, Laino et al (2014) Oral lichen planus: a narrative review. Front Biosci 6:370–376CrossRef
6.
go back to reference Hori S, Nomura T, Sakaguchi S (2003) Control of regulatory T cell development by the transcription factor Foxp3. Science 299:1057–1061CrossRefPubMed Hori S, Nomura T, Sakaguchi S (2003) Control of regulatory T cell development by the transcription factor Foxp3. Science 299:1057–1061CrossRefPubMed
7.
go back to reference Hueber AJ, Asquith DL, Miller AM, Reilly J, Kerr S, Leipe J et al (2010) Cutting edge: mast cells express IL-17A in rheumatoid arthritis synovium. J Immunol 184:3336–3340CrossRefPubMed Hueber AJ, Asquith DL, Miller AM, Reilly J, Kerr S, Leipe J et al (2010) Cutting edge: mast cells express IL-17A in rheumatoid arthritis synovium. J Immunol 184:3336–3340CrossRefPubMed
8.
go back to reference Jontell M, Hansson H-A, Nygren H (1986) Mast cells in oral lichen planus. J Oral Pathol Med 15:273–275CrossRef Jontell M, Hansson H-A, Nygren H (1986) Mast cells in oral lichen planus. J Oral Pathol Med 15:273–275CrossRef
9.
go back to reference Khan A, Farah CS, Savage NW, Walsh LJ, Harbrow DJ, Sugerman PB (2003) Th1 cytokines in oral lichen planus. J Oral Pathol Med 32:77–83CrossRefPubMed Khan A, Farah CS, Savage NW, Walsh LJ, Harbrow DJ, Sugerman PB (2003) Th1 cytokines in oral lichen planus. J Oral Pathol Med 32:77–83CrossRefPubMed
10.
go back to reference Liew F, Pitman N, McInnes I (2010) Disease-associated functions of IL-33: the new kid in the IL-1 family. Nat Rev Immunol 10:103–110CrossRefPubMed Liew F, Pitman N, McInnes I (2010) Disease-associated functions of IL-33: the new kid in the IL-1 family. Nat Rev Immunol 10:103–110CrossRefPubMed
11.
go back to reference Lin AM, Rubin CJ, Khandpur R, Wang JY, Riblett M, Yalavarthi S et al (2011) Mast cells and neutrophils release IL-17 through extracellular trap formation in psoriasis. J Immunol 187:490–500CrossRefPubMedCentralPubMed Lin AM, Rubin CJ, Khandpur R, Wang JY, Riblett M, Yalavarthi S et al (2011) Mast cells and neutrophils release IL-17 through extracellular trap formation in psoriasis. J Immunol 187:490–500CrossRefPubMedCentralPubMed
12.
go back to reference Lodi G, Scully C, Carrozzo M, Griffiths M, Sugerman PB, Thongprasom K (2005) Current controversies in oral lichen planus: report of an international consensus meeting. Oral Surg Oral Med Oral Pathol 100:40–51CrossRef Lodi G, Scully C, Carrozzo M, Griffiths M, Sugerman PB, Thongprasom K (2005) Current controversies in oral lichen planus: report of an international consensus meeting. Oral Surg Oral Med Oral Pathol 100:40–51CrossRef
13.
go back to reference Lu R, Zeng X, Han Q, Lin M, Long L, Dan H et al (2014) Overexpression and selectively regulatory roles of IL-23/Il-17 axis in the lesions of oral lichen planus. Med Inflamm. doi:10.1155/2014/701094 Lu R, Zeng X, Han Q, Lin M, Long L, Dan H et al (2014) Overexpression and selectively regulatory roles of IL-23/Il-17 axis in the lesions of oral lichen planus. Med Inflamm. doi:10.​1155/​2014/​701094
14.
go back to reference O’Connor RACT, Prendergast CA, Sabatos CW (2008) Cutting edge: Th1 cells facilitate the entry of Th17 cells to the central nervous system during experimental autoimmune encephalomyelitis. J. Immunol 181:3750–3754CrossRefPubMedCentralPubMed O’Connor RACT, Prendergast CA, Sabatos CW (2008) Cutting edge: Th1 cells facilitate the entry of Th17 cells to the central nervous system during experimental autoimmune encephalomyelitis. J. Immunol 181:3750–3754CrossRefPubMedCentralPubMed
15.
go back to reference Payeras MR, Cherubini K, Figueiredo MA, Salum FG (2013) Oral lichen planus: focus on etiopathogenesis. Arch Oral Biol 100:1057–1069CrossRef Payeras MR, Cherubini K, Figueiredo MA, Salum FG (2013) Oral lichen planus: focus on etiopathogenesis. Arch Oral Biol 100:1057–1069CrossRef
16.
go back to reference Pereira JS, Monteiro BV, Nonaka CF, Silveira EJ, Miguel MC (2012) FoxP3(+) T regulatory cells in oral lichen planus and its correlation with the distinct clinical appearance of the lesions. Int J Exp Pathol 93:287–294CrossRefPubMedCentralPubMed Pereira JS, Monteiro BV, Nonaka CF, Silveira EJ, Miguel MC (2012) FoxP3(+) T regulatory cells in oral lichen planus and its correlation with the distinct clinical appearance of the lesions. Int J Exp Pathol 93:287–294CrossRefPubMedCentralPubMed
17.
go back to reference Piccirillo CA, Tritt M, Sgouroudis E, Albanese A, Pyzik M, Hay V (2005) Control of type 1 autoimmune diabetes by naturally occurring CD4 + CD25 + regulatory T lymphocytes in neonatal NOD mice. Ann NY Acad Sci 1051:72–87CrossRefPubMed Piccirillo CA, Tritt M, Sgouroudis E, Albanese A, Pyzik M, Hay V (2005) Control of type 1 autoimmune diabetes by naturally occurring CD4 + CD25 + regulatory T lymphocytes in neonatal NOD mice. Ann NY Acad Sci 1051:72–87CrossRefPubMed
18.
go back to reference Shen Z, Gao X, Ma L, Zhou Z, Shen X, Liu W (2014) Expression of Foxp3 and interleukin-17 in lichen planus lesions with emphasis on difference in oral and cutaneous variants. Arch Dermatol Res 306:441–446CrossRefPubMed Shen Z, Gao X, Ma L, Zhou Z, Shen X, Liu W (2014) Expression of Foxp3 and interleukin-17 in lichen planus lesions with emphasis on difference in oral and cutaneous variants. Arch Dermatol Res 306:441–446CrossRefPubMed
19.
go back to reference Sugerman PB, Savage NW, Walsh LJ, Zhao ZZ, Zhou XJ, Khan A et al (2002) The pathogenesis of oral lichen planus. Crit Rev Oral Biol Med 13:350–365CrossRefPubMed Sugerman PB, Savage NW, Walsh LJ, Zhao ZZ, Zhou XJ, Khan A et al (2002) The pathogenesis of oral lichen planus. Crit Rev Oral Biol Med 13:350–365CrossRefPubMed
20.
go back to reference Tao XA, Xia J, Chen XB, Wang H, Dai YH, Rhodus NL et al (2010) FoxP3 + T regulatory cells in lesions of oral lichen planus correlated with disease activity. Oral Dis 16:76–82CrossRefPubMed Tao XA, Xia J, Chen XB, Wang H, Dai YH, Rhodus NL et al (2010) FoxP3 + T regulatory cells in lesions of oral lichen planus correlated with disease activity. Oral Dis 16:76–82CrossRefPubMed
21.
go back to reference Taylor A, Verhagen J, Blaser K, Akdis M, Akdis CA (2006) Mechanisms of immune suppression by interleukin-10 and transforming growth factor-β: the role of T regulatory cells. Immunol 117:433–442CrossRef Taylor A, Verhagen J, Blaser K, Akdis M, Akdis CA (2006) Mechanisms of immune suppression by interleukin-10 and transforming growth factor-β: the role of T regulatory cells. Immunol 117:433–442CrossRef
22.
go back to reference van der Meij EH, van der Waal I (2003) Lack of clinicopathologic correlation in the diagnosis of oral lichen planus based on the presently available diagnostic criteria and suggestions for modifications. J Oral Pathol Med 32:507–512CrossRefPubMed van der Meij EH, van der Waal I (2003) Lack of clinicopathologic correlation in the diagnosis of oral lichen planus based on the presently available diagnostic criteria and suggestions for modifications. J Oral Pathol Med 32:507–512CrossRefPubMed
23.
go back to reference Walsh LJ, Savage NW, Ishii T, Seymour GJ (1990) Immunopathogenesis of oral lichen planus. J Oral Pathol Med 19:389–396CrossRefPubMed Walsh LJ, Savage NW, Ishii T, Seymour GJ (1990) Immunopathogenesis of oral lichen planus. J Oral Pathol Med 19:389–396CrossRefPubMed
24.
go back to reference Zhang l, Yang X-Q, Chen J, Hui R-S, Gao T-W (2010) Increased Th17 cells are accompanied by FoxP3+ Treg cell accumulation and correlated with psoriasis disease severity. Clin Immunol 135:108–117CrossRefPubMed Zhang l, Yang X-Q, Chen J, Hui R-S, Gao T-W (2010) Increased Th17 cells are accompanied by FoxP3+ Treg cell accumulation and correlated with psoriasis disease severity. Clin Immunol 135:108–117CrossRefPubMed
25.
go back to reference Zhou XJ, Sugerman PB, Savage NW, Walsh LJ, Seymour GJ (2002) Intra-epithelial CD8+ T cell and basement membrane disruption in oral lichen planus. J Oral Pathol Med 31:23–27CrossRefPubMed Zhou XJ, Sugerman PB, Savage NW, Walsh LJ, Seymour GJ (2002) Intra-epithelial CD8+ T cell and basement membrane disruption in oral lichen planus. J Oral Pathol Med 31:23–27CrossRefPubMed
Metadata
Title
Regulation of immune cells in oral lichen planus
Authors
F. A. Firth
L. T. Friedlander
V. P. B. Parachuru
T. B. Kardos
G J. Seymour
A. M. Rich
Publication date
01-05-2015
Publisher
Springer Berlin Heidelberg
Published in
Archives of Dermatological Research / Issue 4/2015
Print ISSN: 0340-3696
Electronic ISSN: 1432-069X
DOI
https://doi.org/10.1007/s00403-015-1540-8

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