Regulatory T cells in the actinic cheilitis
Background Actinic cheilitis (AC) is an oral potentially malignant lesion which is the counterpart of actinic keratosis of the skin and has potential to develop into squamous cell carcinoma. Regulatory T cells (Tregs) have a critical role in modulating the antitumor immune responses. The presence of...
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Published in | Journal of oral pathology & medicine Vol. 43; no. 10; pp. 754 - 760 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frederiksberg
Blackwell Publishing Ltd
01.11.2014
Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Actinic cheilitis (AC) is an oral potentially malignant lesion which is the counterpart of actinic keratosis of the skin and has potential to develop into squamous cell carcinoma. Regulatory T cells (Tregs) have a critical role in modulating the antitumor immune responses. The presence of regulatory T cells in potentially malignant lesions has not been described. We chose investigate the involvement of regulatory T cells in potentially malignant lesions.
Methods
The frequency, phenotype, and activity of CD4+CD25+ T cells isolated from blood and lesion of AC patients were analyzed by flow cytometry. Cytokines were quantified by ELISA. Data were compared with samples from healthy subjects.
Results
The frequency and suppressor activity of circulating CD4+CD25+ T cells was similar in AC patients and control subjects. However, the frequencies of IL‐10‐positive Tregs were higher in AC patients, and these cells inhibited interferon‐gamma (IFN‐γ) and increased interleukin (IL)‐10 productions in co‐cultures. Furthermore, CD4+CD25+ T cells accumulate in AC lesions. Lesions‐derived regulatory T cells suppressed lymphocyte proliferation and pro‐inflammatory cytokine production. Moreover, high levels of IL‐10 and transforming growth factor‐β (TGF‐β), and low IFN‐γ were detected in the potentially malignant lesions.
Conclusion
Therefore, our data show that Tregs accumulate in AC lesions, and these cells could be suppressing immune responses in a potentially malignant microenvironment. |
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Bibliography: | Fundação de Amparo à Pesquisa do Estado de São Paulo-FAPESP - No. 2006/04264-9; No. 2009/14127-7 Conselho Nacional de Desenvolvimento Científico e Tecnológico istex:38C928F5AE2849B6C5B2DC2E1934F6BE5FD9B15F ArticleID:JOP12207 Coordenação de Aperfeiçoamento de Pessoal de Nível ark:/67375/WNG-Z5Q11GT8-3 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0904-2512 1600-0714 |
DOI: | 10.1111/jop.12207 |