Immune response and evasion mechanisms in lip carcinogenesis: An immunohistochemical study

Programmed death ligand-1 (PD-L1) and human leukocyte antigen-G (HLA-G) are considered immune checkpoint molecules that inhibit T-cell effectiveness, contributing to tumor immune escape. This study investigated PD-L1, HLA-G, CD8, and granzyme B (GrB) expression at different stages of lip carcinogene...

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Veröffentlicht in:Archives of oral biology 2019-02, Vol.98, p.99
Hauptverfasser: Lopes, Maria Luiza Diniz de Sousa, Gonzaga, Amanda Katarinny Goes, Mosconi, Carla, Palomino, Gustavo Martelli, Mendonça, Elismauro Francisco, Batista, Aline Carvalho, Silveira, Éricka Janine Dantas da
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Sprache:eng
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Zusammenfassung:Programmed death ligand-1 (PD-L1) and human leukocyte antigen-G (HLA-G) are considered immune checkpoint molecules that inhibit T-cell effectiveness, contributing to tumor immune escape. This study investigated PD-L1, HLA-G, CD8, and granzyme B (GrB) expression at different stages of lip carcinogenesis. Forty cases of lip squamous cell carcinoma (LSCC), 55 actinic cheilitis (AC), and 10 healthy lip mucosa (HLM) were submitted to immunohistochemistry. Semiquantitative (PD-L1, HLA-G), and quantitative (CD8, GrB) analysis were performed. PD-L1 and HLA-G expression in neoplastic cells/keratinocytes and stroma/connective tissue was significantly higher in LSCC and AC, compared to HLM (p
ISSN:1879-1506
DOI:10.1016/j.archoraibio.2018.09.017