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DOI 10.1111/j.1601-0825.2012.01960.x

Медицинская библиотека · Oral diseases · 2012

Immunophenotypic characterization and distribution of dendritic cells in odontogenic cystic lesions.

Matos F T C, Rizo V H T, Almeida L Y, Tirapelli C, Silva-Sousa Y T C, Almeida O P, León J E

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

To analyze the expression and distribution patterns of mature dendritic cells (mDCs) and immature DCs (imDCs) in radicular cysts (RCs), dentigerous cysts (DtCs), and keratocystic odontogenic tumors (KCOTs).

MATERIALS AND

METHODS

Forty-nine odontogenic cystic lesions (OCLs) (RCs, n = 20; DtCs, n = 15; KCOTs, n = 14) were assessed using the following markers: S100, CD1a and CD207 for imDCs; and CD83 for mDCs.

RESULTS

Almost all cases were S100, CD1a, and CD207 positive, whereas 63% were CD83 positive. RCs presented greater number of immunostained cells, followed by DtCs, and KCOTs. The number of S100+ cells was greater than both CD1a+ and CD207+ cells (P < 0.001), which showed approximately similar amounts, followed by lower number of CD83+ cells (P < 0.001) in each OCL type. Different from S100+ cells, both CD1a+ and CD207+ cells on the epithelium (P < 0.05) and CD83+ cells on the capsule (P < 0.05) were preferentially observed. In RCs, significant correlation was found between the thickness epithelium with S100+ and CD1a+ cells, and between the degree of inflammation with CD83+ cells.

CONCLUSIONS

Dendritic cell populations in OCLs can be phenotypically heterogeneous, and it could represent distinct lineages and/or functional stages. It is suggested that besides DC-mediated immune cell interactions, DC-mediated tissue differentiation and maintenance in OCLs should also be considered.

Для цитирования: Matos F T C, Rizo V H T, Almeida L Y, Tirapelli C, Silva-Sousa Y T C, Almeida O P, León J E. Immunophenotypic characterization and distribution of dendritic cells in odontogenic cystic lesions.. Oral diseases. 2012. DOI: 10.1111/j.1601-0825.2012.01960.x.

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