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 inJournal of oral pathology & medicine Vol. 43; no. 10; pp. 754 - 760
Main Authors Gasparoto, Thaís Helena, de Souza Malaspina, Tatiana Salles, Damante, José Humberto, de Mello Jr, Edgard Franco, Ikoma, Maura Rosane Valério, Garlet, Gustavo Pompermaier, Costa, Maria Renata Sales Nogueira, Cavassani, Karen Angélica, da Silva, João Santana, Campanelli, Ana Paula
Format Journal Article
LanguageEnglish
Published Frederiksberg Blackwell Publishing Ltd 01.11.2014
Wiley
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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.
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